Adjunct Professor Ann Bye | Brain Sciences UNSW

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University role:

Conjoint Associate Professor

Phone:

(02) 9382 1549

Email:

a.bye@unsw.edu.au

Dr Annie Bye OAM is a Conjoint Associate Professor in the Discipline of Paediatrics in the School of Women's & Children's Health. She is a Senior Paediatric Neurologist at Sydney Children’s Hospital and Departmental Head.

Memberships:

Australian & New Zealand Association of Neurologists
Royal Australian College of Physicians
Australian College of Paediatrics
Australian Child Neurology Study Group
National Epilepsy Association of Australia
Epilepsy Society of NSW (formerly Vice-President of the Epilepsy Society of Australia) 2012-2014
Member Scientific Committee Epilepsy Society of Australia 2022

Qualifications:

MB BS Syd, FRACP, Doctorate of Medicine

OAM

Grants:

Se CV

2022 NHMRC Grant 2011481: Characterisation of novel genetic variants in Hyperekplexia and Dravet Syndrome. Chief Investigator: Associate Professor Seo-Kyung Chung Head, Translational Neurogenomics Research Group, Faculty of Medicine and Health, University of Sydney. (Associate investigator: Ann Bye et al). Amount (2022-2024): $585,714.50

2021 Sydney Children’s Hospital Network Early Career Researcher Award - Suzanne Nevin (PhD candidate): Kids Research at The Sydney Children’s Hospitals Network and Sydney Children’s Hospitals Foundation. Senior Chief Investigator: AME Bye. Amount (2021-2022): $20,000

2021 Manildra Foundation – administered via UNSW (Philanthropic Research Grant)

ClinEquip: Development and evaluation of resources for carers and clinicians involved in care of children with severe genetic epilepsies. $150,000. Chief Investigators: A Bye, K Nunn)

2020 Manildra Foundation – administered via UNSW (Philanthropic Research Grant): GeneCompass

Pilot study, new model of care in severe genetic epilepsy. Amount: $265,000 Chief Investigator: A Bye, E Palmer

2019 /2020 SPHERE funding for CoGENES project Officer: Improving clinical care and support for children with severe early-onset epilepsies and their families. Investigators: Rebecca Macintosh, Sean Kennedy, Rani Sachdev, Annie Bye, Hugh McCarthy, Emma Palmer, Claire Wakefield. Amount (2019): $17,000; 2020 Amount: $36,690

2018 SCHN Foundation: Improving support and providing integrated care for children with chronic genetic conditions. Investigators: R. Macintosh, S. Kennedy, R. Sachdev, A. Bye, H. McCarthy, C. Wakefield. Amount (2018): $20,000

2016 NSW Genomics Collaborative Grants: Drug resistant childhood onset epilepsy with intellectual disability: leveraging genomic sequencing to identify novel genes and neurodevelopmental pathways and determine optimal diagnostic protocols. Collaborative grant (member of the NSW collaboration led by Prof Edward Kirk, SCH, UNSW). Amount: $180,000

2016 NHMRC PhD Scholarship (Dr Emma Palmer): Application of next generation sequencing for the diagnosis of epileptic encephalopathy – the science, the costings and the impact. PhD Supervisors Edwin Kirk and Annie Bye. Amount: $127,000

2016 Michelle Beets Award (Humpty Dumpty Charity) : Used for infrastructure/resources and implementation of EEG service SCH. Annie Bye. Amount: $20,000

2016 /2017 NSW HEALTH GRANTS (Children’s Healthcare Network, NSW Health) Chief Investigator: A Bye. Modification of App based on scientific study Efficacy. Amount: $15,290

2015 /16 NSW HEALTH GRANTS (Children’s Healthcare Network, NSW Health): Chief Investigator: A Bye. Development of App for education of adolescents in epilepsy. Phase 2 Scientific Study of Evaluation. Amount: $35,000

2014 NSW HEALTH GRANTS (Children’s Healthcare Network, NSW Health): Chief Investigator: A Bye. Development of Paediatric Epilepsy Network NSW. Website Educational Resource in Epilepsy for Paediatricians and Families: Amount: $82,.800

2014 /15 NSW HEALTH GRANTS (Children’s Healthcare Network, NSW Health): Chief Investigator: A Bye. Development of App for education of adolescents in epilepsy. Phase 1 Amount: $65,100

2013 NSW HEALTH GRANTS (Children’s Healthcare Network, NSW Health): Chief Investigator: A Bye. Development: Paediatric Epilepsy Network NSW - Website Educational Resource for Paediatricians and Families. Amount: $48,000

Awards:

1974

Robert Scot Skirving Memorial Prize in Medicine and Surgery

1974

Harold John Ritchie Memorial Prize

in Clinical Medicine

2007

Paediatric Teaching Award: Senior Staff Member

UNSW School of Women’s and Children’s Health Disciple of Paediatrics

2008

Excellence in Teaching Award Senior Consultant: Inaugural Presentation

Sydney Children’s Hospital

2010

Excellence in Teaching Award Senior Consultant

Sydney Children’s Hospital

2011

Excellence in Teaching Award Senior Consultant

Sydney Children’s Hospital

2012

Michelle Beets Memorial Award 2012

Humpty Dumpty Foundation ($20,000 awarded)

For services to paediatric epilepsy

2013

Highly Commended

SCHN Quality and Innovation Awards: “Supporting clinicians and families to improve the care of children and adolescents with epilepsy across NSW: the paediatric epilepsy network NSW (PENNSW).”

2014

Paediatrics Staff Award: Senior Staff Research

UNSW School of Women’s and Children’s Health

2016

Finalist (Highly Commended) – SCHN Quality Improvement Awards

Development & evaluation of an E-learning resource on approach to first seizure.

2017

Finalist – SCHN Quality Improvement Awards

An app for adolescents with epilepsy: design and evaluation of EpApp.

Order of Australia

2016

The Order of Australia - Appointed as member in the general division (OAM)

For Services to Paediatric Neurology

For significant service to medicine in the field of paediatric neurology as a clinician, academic and mentor.

Research

Research activities:

Conjoint A/Prof Annie Bye has an extensive portfolio of research into paediatric epilepsy and neurology, with over 90 original research articles together with over 100 abstracts published in international and national peer reviewed journals. Research topics include neonatal seizures, neuropsychological and language profiles in paediatric epilepsy, MRI correlates of childhood epilepsy syndromes, quality of life in paediatric epilepsy, the neurogenetic profiles of severe drug resistant epilepsies and education of epilepsy to patients and medical staff. This research has been supported by NHMRC, Ramichotti, Brain Foundation and Sydney Children’s Hospital Foundation funding bodies. She was awarded her MD for publications in epilepsy in 1996

Current Research Projects:

1) Pilot evaluation of Gene Compass, an information linker service that provides caregivers with personalised reports in response to their specific questions about their child's condition.

2. Exploration of the psychological burdens of health professionals managing patients with severe genetic epilepsies and development of resources to assist skill formation and resilience in this area.

3) Paediatric Epilepsy Network

This is a major project to raise minimal standards of care in management of paediatric epilepsy across NSW. This work commenced in 2010. It has been funded by NSW Health (Statewide Complex Epilepsy, NSW Kids and Families). A GAP analysis was done to determine needs of paediatricians across NSW. In response to a need for easily assessable, evidence based educational resources a website was created- PENNSW. This resource has two sections, one for clinicians and one for families. It has information on epilepsy syndromes, medications, lifestyle implications-employment, pregnancy, contraception, driving. Key documents for safety, seizure management plan, medication plans, seizure recording are available. The website was evaluated.( Journal of Clinical Neuroscience : 21 (2014) 1831-1832) Currently it has approximately 352,000 views, 100, 000 in last 7 months. Sept 2015. Subsequent to this an E-Learning Package for First Unprovoked Seizure has been developed, validated and published. An APP for education of teenagers with epilepsy with a functional component for seizure tracking and medication reminder has been developed and also validated and the work published.

4.Evaluation of educational programmes for paediatricians. The first involves an assessment of an outreach teaching programme of neurology to paediatricians. The second is an evaluation of recorded webinars in a series of paediatric topics and comparison to face to face teaching.

Research Collaborations:

A present major work is one in conjunction with her colleagues across the Sydney Children’s Hospital Network Randwick and Westmead campus and the John Hunter Hospital to evaluate and improve epilepsy services for children across the State of NSW. This has resulted in the formation of the Paediatric Epilepsy Network NSW website www.pennsw.com.au

Research Interests:

Current major interests are the scientific evaluation of teaching programmes directed to paediatricians and evaluation of an information linker directed to the caregivers of patients with severe genetic epilepsy (see above). the other major interest is exploration of the psychological burdens places on health professionals assisting families of children with severe genetic epilepsy and building resources to support them informed by the work.

Field of Research (FOR) Tag:

Paediatrics

Neurology and Neuromuscular Diseases

Socio-economic Objective (SEO) tags:

Child health

Teaching & Supervision

I am available to supervise:

Areas of supervision:

As a paediatric neurologist my major academic interest is clinical research of paediatric epilepsy. I have an extensive portfolio with over 90 original research articles published in international and national high impact peer reviewed journals. Research epilepsy topics include neonatal seizures, neuropsychological and language profiles in paediatric epilepsy, MRI correlates of childhood epilepsy syndromes, quality of life in paediatric epilepsy, childhood epilepsy with centrotemporal spikes, temporal lobe dysplasia and associated pathologies in an adult and paediatric surgical cohort.

From 2013 with the increasing impact of gene discovery, I concentrated on the genetic aspects of developmental epileptic encephalopathy with the supervision of a PhD undertaken by Emma Palmer. We interrogated a cohort of 45 children with undiagnosed severe infantile epilepsies using whole genome sequencing, evaluating cost effectiveness and facilitation of functional studies in selected targeted genes with international collaborators. This work led to increasing awareness of the psychological needs of caregivers of severe genetic epilepsies and clinician burden navigating management in this area. The PhD of Suzanne Nevin accepted 2022, addressed caregiver need and resulted in the psychological resource “Finding A Way”.

Current research focuses on a continuation of this work: A pre-post pilot evaluation of “GenE Compass”- Linking families and clinicians with the highest quality information about developmental and epileptic encephalopathies (Postdoctorate Researcher, Eden Robinson, ethics approved, in analytic phase); and a second project: ‘ClinEquip: equipping clinicians to navigate and manage severe neurogenetic disease’ - codesign and development of positive psychology informed resources for clinicians managing patients with severe, rare neurogenetic diseases (Post doctorate Researcher Suzanne Nevin, ethics accepted – include HREC number).

My third area of research is the evaluation of teaching and information provision to patients, clinicians and medical students with the development of a number of resources, many assessed scientifically.

Publications: Impact factor >5: Epilepsia (10), Neurology (6), (Developmental Medicine Child Neurology (7), Nature Genetics (2) American Journal Human Genetics(2) British Journal Pharmacology (1), Medical Journal Australia (1), European Journal Nuclear Medicine (1), Molecular Neurobiology (1), Frontiers in Immunology (1), Human Molecular Genetics (1), Cell Reports (1), Cell (1), Medical Education (1). H Index: 29 (CV p12-15)

The above research profile involved supervision of 11 higher degrees: 4 PhDs, a Doctorate of Clinical Neuropsychology, 5 Masters and an Honours degree to successful completion. (CV p6)

The research was funded by 3 NHMRC grants, NHMRC PhD scholarship Emma Palmer, Ramichotti, Financial Markets, 5 Brain Foundation Grants, 10 Sydney Children Hospital Grants, 4 NSW Health Grants, NSW Genomics Collaborative Grant; Philanthropy: Manildra Foundation. (CV p8-11)

Current collaborators include national and international workers in field. (CV p22-23)

This research has made a significant contribution to the understanding and phenotyping of childhood epilepsy, added to genetic interrogation of developmental epileptic encephalopathies preparing for precision medicine and resulted in development/evaluation of educational and psychology based tools for clinicians and families coping with rare neurogenetic disorders.

Currently supervising:

Suzanne Nevin: Post doctorate in project known as Gene-Equip exploring the needs of cinicians in managing patients with severe genetic epilepsies.

The methodology is to define the problem, understand the reasons for it and then provide solutions through interview and workshops.

The ultimate aim is to create resources informed by the research to empower and assist clinicians, health professionals and students.

Supervision keywords:

paediatric neurology

genomics

mental health

Teaching:

A/Prof Bye has had a longstanding interest in education of medical students and junior medical staff, allied health and patients. She has supervised young doctors in medical training and research and has published on teaching techniques. Recently she has been involved in the development of a published tool to teach adolescents about the challenges of epilepsy in all aspects of their lives- issues such as driving, pregnancy and contraception, life style and career.

The UNSW Health and Medicine Strategy, Health 25 is to build a vibrant learning community: one that works in equitable partnership with students. This has been my philosophy and since my appointment at Sydney Children’s Hospital and Conjoint appointment at UNSW I have strived to do this and teaching at this point is a major commitment.

I have served as a Principal medical student teacher 1-2 terms per year 1987- 2019. As a Principal Teacher I gave tutorials weekly and did much bedside teaching and took student grand rounds. I have given formal medical student lectures from my earliest Conjoint appointment to the present, a minimum of 10 lectures per year on aspects of epilepsy (till 2016) and currently 5/year. From 1991-2011 I gave 4 lectures/ year to Diploma of Paediatric students (SCH/UNSW) and was a regular examiner. From 1987-2011. I was a regular, medical student examiner for the viva short case sessions. From 2011-2019 I have performed many Mini-CEXs when Principal teacher. Throughout my appointment as a conjoint I have regularly (twice weekly) had medical students in my outpatients. Medical students regularly attend our weekly Neurology Grand Rounds and my teaching to junior staff, particularly a series of 6 sessions given annually on “Neurological Gait” illustrated by video. In COVID I gave extra online sessions to students: case presentations, and online teaching of normal development using the resource “Beyond Milestones”. As part of the hospital COVID response team I recruited other teachers. From 2008 I have given weekly epilepsy teaching sessions to medical students and junior staff. As Head of Department, I arranged medical student teaching rosters 2012-2019 and championed teaching.

Following cessation of my clinical on-call and ward duties (2020-2021), I developed new ways of serving students. I recently led a team in the production of educational resources (CV p24-25). These are given to all UNSW students. These include: a Website-PENNSW providing epilepsy resources for students, clinicians and families, First Seizure E-Learning resource, a video series teaching normal development, “Beyond Milestones”, 4 videos on aspects of childhood epilepsy management ( “First seizure”, “Using Midazolam”, “Living well with Epilepsy”, educational resource for adolescence, “The Ketogenic diet”-an Introduction and, released to medical students in 2022, “Finding A Way”, a six module Positive Psychology informed video resource for parents of children with severe genetic epilepsy.

I have researched my techniques in teaching medical students and evaluated many of above resources in 8 published papers related to educational research (CV p25).

My teaching extends to: The Royal Australian College of Physicians (Basic trainees) and College Brain School for Paediatric Neurology trainees, the annual Masterclass and EEG National courses for all Neurology trainees and annual SCH Course in Paediatrics. I have given many invited National/ International presentations (CV p24-33).

In 2017 I began an online neurology teaching program for Paediatricians, Junior Staff and Medical Students involving case presentations, mini-lectures and question time. Rotating UNSW medical students in neurology attend as do medical students from 7 UNSW teaching hospitals.

Media

Facebook:

https://www.facebook.com/UNSWPaediatrics

Publications related to this Person

Journal articles

Nevin SM; Wakefield CE; Barlow-Stewart K; McGill BC; Bye A; Palmer EE; Dale RC; Gill D; Kothur K; Boggs K; Le Marne F; Beavis E; Macintosh R; Sachdev R, 2022, 'Psychosocial impact of genetic testing on parents of children with developmental and epileptic encephalopathy', Developmental Medicine and Child Neurology, vol. 64, pp. 95 - 104, http://dx.doi.org/10.1111/dmcn.14971

Nevin SM; Wakefield CE; Dadich A; LeMarne F; Macintosh R; Beavis E; Sachdev R; Bye A; Nunn K; Palmer EE, 2022, 'Hearing parents' voices: A priority-setting workshop to inform a suite of psychological resources for parents of children with rare genetic epilepsies', PEC Innovation, vol. 1, pp. 100014 - 100014, http://dx.doi.org/10.1016/j.pecinn.2021.100014

Palmer EE; Sachdev R; Macintosh R; Melo US; Mundlos S; Righetti S; Kandula T; Minoche AE; Puttick C; Gayevskiy V; Hesson L; Idrisoglu S; Shoubridge C; Thai MHN; Davis RL; Drew AP; Sampaio H; Andrews PI; Lawson J; Cardamone M; Mowat D; Colley A; Kummerfeld S; Dinger ME; Cowley MJ; Roscioli T; Bye A; Kirk E, 2021, 'Diagnostic Yield of Whole Genome Sequencing After Nondiagnostic Exome Sequencing or Gene Panel in Developmental and Epileptic Encephalopathies', Neurology, vol. 96, pp. e1770 - e1782, http://dx.doi.org/10.1212/WNL.0000000000011655

Ng EWM; Le Marne F; Sinclair KG; Lorentzos MS; Waak M; Deuble N; Georgeson T; Rao A; Rikhi S; Mallitt KA; Bye A, 2021, 'Evaluation of an educational video providing key messages for doctors to counsel families following a first afebrile seizure', Journal of Paediatrics and Child Health, vol. 57, pp. 198 - 203, http://dx.doi.org/10.1111/jpc.15171

Kelada L; Wakefield CE; Drew D; Ooi CY; Palmer EE; Bye A; De Marchi S; Jaffe A; Kennedy S, 2021, 'Siblings of young people with chronic illness: Caring responsibilities and psychosocial functioning', Journal of Child Health Care, pp. 13674935211033466, http://dx.doi.org/10.1177/13674935211033466

Palmer EE; Carroll R; Shaw M; Kumar R; Minoche AE; Leffler M; Murray L; Macintosh R; Wright D; Troedson C; McKenzie F; Townshend S; Ward M; Nawaz U; Ravine A; Runke CK; Thorland EC; Hummel M; Foulds N; Pichon O; Isidor B; Le Caignec C; Demeer B; Andrieux J; Albarazi SH; Bye A; Sachdev R; Kirk EP; Cowley MJ; Field M; Gecz J, 2020, 'RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features', American Journal of Human Genetics, vol. 107, pp. 1157 - 1169, http://dx.doi.org/10.1016/j.ajhg.2020.10.005

Balestrini S; Mikati MA; Álvarez-García-Rovés R; Carboni M; Hunanyan AS; Kherallah B; McLean M; Prange L; De Grandis E; Gagliardi A; Pisciotta L; Stagnaro M; Veneselli E; Campistol J; Fons C; Pias-Peleteiro L; Brashear A; Miller C; Samões R; Brankovic V; Padiath QS; Potic A; Pilch J; Vezyroglou A; Bye AME; Davis AM; Ryan MM; Semsarian C; Hollingsworth G; Scheffer IE; Granata T; Nardocci N; Ragona F; Arzimanoglou A; Panagiotakaki E; Carrilho I; Zucca C; Novy J; Dzieżyc K; Parowicz M; Mazurkiewicz-Bełdzińska M; Weckhuysen S; Pons R; Groppa S; Sinden DS; Pitt GS; Tinker A; Ashworth M; Michalak Z; Thom M; Cross JH; Vavassori R; Kaski JP; Sisodiya SM, 2020, 'Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study.', Neurology, vol. 95, pp. e2866 - e2879, http://dx.doi.org/10.1212/WNL.0000000000010794

Nevin SM; Wakefield CE; Schilstra CE; McGill BC; Bye A; Palmer EE, 2020, 'The information needs of parents of children with early-onset epilepsy: A systematic review', Epilepsy and Behavior, vol. 112, pp. 107382 - 107382, http://dx.doi.org/10.1016/j.yebeh.2020.107382

Le Marne FA; Towns SJ; Gaskin C; Ho J; Baker R; Beavis E; Bye AM, 2019, 'Implementing a new adolescent epilepsy service: Improving patient experience and readiness for transition', Journal of Paediatrics and Child Health, vol. 55, pp. 819 - 825, http://dx.doi.org/10.1111/jpc.14301

Palmer EE; Hong S; Al Zahrani F; Hashem MO; Aleisa FA; Ahmed HMJ; Kandula T; Macintosh R; Minoche AE; Puttick C; Gayevskiy V; Drew AP; Cowley MJ; Dinger M; Rosenfeld JA; Xiao R; Cho MT; Yakubu SF; Henderson LB; Guillen Sacoto MJ; Begtrup A; Hamad M; Shinawi M; Andrews MV; Jones MC; Lindstrom K; Bristol RE; Kayani S; Snyder M; Villanueva MM; Schteinschnaider A; Faivre L; Thauvin C; Vitobello A; Roscioli T; Kirk EP; Bye A; Merzaban J; Jaremko Ł; Jaremko M; Sachdev RK; Alkuraya FS; Arold ST, 2019, 'De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-Progressive Neurocognitive Syndrome', American Journal of Human Genetics, vol. 104, pp. 542 - 552, http://dx.doi.org/10.1016/j.ajhg.2019.01.013

Tea F; Lopez JA; Ramanathan S; Merheb V; Lee FXZ; Zou A; Pilli D; Patrick E; van der Walt A; Monif M; Tantsis EM; Yiu EM; Vucic S; Henderson APD; Fok A; Fraser CL; Lechner-Scott J; Reddel SW; Broadley S; Barnett MH; Brown DA; Lunemann JD; Dale RC; Brilot F; Sinclair A; Kermode AG; Kornberg A; Bye A; McGettigan B; Trewin B; Brew B; Taylor B; Bundell C; Miteff C; Troedson C; Pridmore C; Spooner C; Yiannikas C; O'Gorman C; Clark D; Suan D; Jones D; Kilfoyle D; Gill D; Wakefield D; Hofmann D; Mathey E; O'Grady G; Jones HF; Beadnall H; Butzkueven H; Joshi H; Andrews I; Sutton I; MacIntyre J; Sandbach JM; Freeman J; King J; O'Neill JH; Parratt J; Barton J; Garber J; Ahmad K; Riney K; Buzzard K; Kothur K; Cantrill LC; Menezes MP; Paine MA; Marriot M; Ghadiri M; Boggild M; Lawlor M; Badve M; Ryan M; Aaqib M; Shuey N; Jordan N; Urriola N; Lawn N; White O; McCombe P; Patel R; Leventer R; Webster R; Smith R; Gupta S; Mohammad SS; Pillai S; Hawke S; Simon S; Calvert S; Blum S; Malone S; Hodgkinson S; Nguyen TK; Hardy TA; Kalincik T; Ware T; Fung VSC, 2019, 'Characterization of the human myelin oligodendrocyte glycoprotein antibody response in demyelination', Acta Neuropathologica Communications, vol. 7, http://dx.doi.org/10.1186/s40478-019-0786-3

Le Marne FA; Butler S; Beavis E; Gill D; Bye AME, 2018, 'EpApp: Development and evaluation of a smartphone/tablet app for adolescents with epilepsy', Journal of Clinical Neuroscience, vol. 50, pp. 214 - 220, http://dx.doi.org/10.1016/j.jocn.2018.01.065

Palmer EE; Schofield D; Shrestha R; Kandula T; Macintosh R; Lawson JA; Andrews I; Sampaio H; Johnson AM; Farrar MA; Cardamone M; Mowat D; Elakis G; Lo W; Zhu Y; Ying K; Morris P; Tao J; Dias KR; Buckley M; Dinger ME; Cowley MJ; Roscioli T; Kirk EP; Bye A; Sachdev RK, 2018, 'Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness', Molecular Genetics and Genomic Medicine, vol. 6, pp. 186 - 199, http://dx.doi.org/10.1002/mgg3.355

Gennarino VA; Palmer EE; McDonell LM; Wang L; Adamski CJ; Koire A; See L; Chen CA; Schaaf CP; Rosenfeld JA; Panzer JA; Moog U; Hao S; Bye A; Kirk EP; Stankiewicz P; Breman AM; McBride A; Kandula T; Dubbs HA; Macintosh R; Cardamone M; Zhu Y; Ying K; Dias KR; Cho MT; Henderson LB; Baskin B; Morris P; Tao J; Cowley MJ; Dinger ME; Roscioli T; Caluseriu O; Suchowersky O; Sachdev RK; Lichtarge O; Tang J; Boycott KM; Holder JL; Zoghbi HY, 2018, 'A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures', Cell, vol. 172, pp. 924 - 936.e11, http://dx.doi.org/10.1016/j.cell.2018.02.006

Said M; Uppal P; Bye A; Palasanthiran P, 2018, 'Unusual case of tuberculous meningitis with discordant ventricular and lumbar cerebrospinal fluid; lessons in the era of world-wide migration', Journal of Paediatrics and Child Health, vol. 54, pp. 93 - 95, http://dx.doi.org/10.1111/jpc.13665

Gururaj S; Palmer EE; Sheehan GD; Kandula T; Macintosh R; Ying K; Morris P; Tao J; Dias KR; Zhu Y; Dinger ME; Cowley MJ; Kirk EP; Roscioli T; Sachdev R; Duffey ME; Bye A; Bhattacharjee A, 2017, 'A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic Encephalopathy', Cell Reports, vol. 21, pp. 926 - 933, http://dx.doi.org/10.1016/j.celrep.2017.09.088

Palmer EE; Sachdev R; Kandula T; Macintosh R; Kirk E; Bye A, 2017, 'Genetics of Epileptic Encephalopathies', eLS, pp. 1 - 11, http://dx.doi.org/10.1002/9780470015902.a0026922

Johnson AM; Sugo E; Barreto D; Hiew CC; Lawson JA; Connolly AM; Somerville E; Hasic E; Bye AM; Cunningham AM, 2016, 'The Severity of Gliosis in Hippocampal Sclerosis Correlates with Pre-Operative Seizure Burden and Outcome After Temporal Lobectomy', Molecular Neurobiology, vol. 53, pp. 5446 - 5456, http://dx.doi.org/10.1007/s12035-015-9465-y

Le Marne FA; McGinness H; Slade R; Cardamone M; Balbir Singh S; Connolly AM; Bye AME, 2016, 'Evaluation of an E-learning resource on approach to the first unprovoked seizure', Journal of Paediatrics and Child Health, vol. 52, pp. 896 - 900, http://dx.doi.org/10.1111/jpc.13277

Palmer EE; Jarrett KE; Sachdev RK; Zahrani FA; Hashem MO; Ibrahim N; Sampaio H; Kandula T; Macintosh R; Gupta R; Conlon DM; Billheimer JT; Rader DJ; Funato K; Walkey CJ; Lee CS; Loo C; Brammah S; Elakis G; Zhu Y; Buckley M; Kirk EP; Bye A; Alkuraya FS; Roscioli T; Lagor WR, 2016, 'Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathy', Human Molecular Genetics, vol. 25, pp. 3042 - 3054, http://dx.doi.org/10.1093/hmg/ddw157

Palmer EE; Hayner J; Sachdev R; Cardamone M; Kandula T; Morris P; Dias KR; Tao J; Miller D; Zhu Y; Macintosh R; Dinger ME; Cowley MJ; Buckley MF; Roscioli T; Bye A; Kilberg MS; Kirk EP, 2015, 'Asparagine Synthetase Deficiency causes reduced proliferation of cells under conditions of limited asparagine', Molecular Genetics and Metabolism, vol. 116, pp. 178 - 186, http://dx.doi.org/10.1016/j.ymgme.2015.08.007

Connolly AM; Beavis E; Mugica-Cox B; Bye AME; Lawson JA, 2015, 'Exploring carer perceptions of training in out-of-hospital use of buccal midazolam for emergency management of seizures (2008-2012)', Journal of Paediatrics and Child Health, vol. 51, pp. 704 - 707, http://dx.doi.org/10.1111/jpc.12811

Johnson AM; Sugo E; Barreto D; Cunningham AM; Hiew CC; Lawson JA; Somerville ER; Connolly AM; Bye AME, 2014, 'Response to "About Focal Cortical Dysplasia (FCD) type IIIa"', Epilepsy Research, vol. 108, pp. 1958 - 1959, http://dx.doi.org/10.1016/j.eplepsyres.2014.09.027

Connolly AM; Slade R; Uppal P; Bye AME, 2014, 'Caring for children and adolescents with epilepsy: Creating an innovative electronic educational resource', Journal of Clinical Neuroscience, vol. 21, pp. 1831 - 1832, http://dx.doi.org/10.1016/j.jocn.2014.02.019

Johnson AM; Sugo E; Barreto D; Cunningham AM; Hiew CC; Lawson JA; Somerville ER; Connolly AM; Bye AME, 2014, 'Clinicopathological associations in temporal lobe epilepsy patients utilising the current ILAE focal cortical dysplasia classification', Epilepsy Research, vol. 108, pp. 1345 - 1351, http://dx.doi.org/10.1016/j.eplepsyres.2014.06.013

Connolly AM; Cunningham C; Sinclair AJ; Rao A; Lonergan A; Bye AME, 2014, ''Beyond Milestones': A randomised controlled trial evaluating an innovative digital resource teaching quality observation of normal child development', Journal of Paediatrics and Child Health, vol. 50, pp. 393 - 398, http://dx.doi.org/10.1111/jpc.12485

Morton NJ; Palasanthiran P; Bye A; Sugo E; Snelling TL; Britton P; Kesson A; Ardern-Holmes S, 2013, 'Severe hemorrhagic meningoencephalitis due to angiostrongylus cantonensis among young children in Sydney, Australia', Clinical Infectious Diseases, vol. 57, pp. 1158 - 1161, http://dx.doi.org/10.1093/cid/cit444

Carvill GL; Heavin SB; Yendle SC; McMahon JM; O'Roak BJ; Cook J; Khan A; Dorschner MO; Weaver M; Calvert S; Malone S; Wallace G; Stanley T; Bye AME; Bleasel AF; Howell KB; Kivity S; Mackay MT; Rodriguez-Casero V; Webster R; Korczyn AD; Afawi Z; Zelnick N; Lerman-Sagie T; Lev D; Moller RS; Gill D; Andrade DM; Freeman JL; Sadleir LG; Shendure JA; Berkovic SF; Scheffer IE; Mefford HC, 2013, 'Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1', Nature Genetics, vol. 45, pp. 825 - 830, http://dx.doi.org/10.1038/ng.2646

Connolly AM; Cunningham C; Sinclair AJ; Lonergan A; Bye AM; Rao A, 2013, ''Beyond Milestones': A randomised controlled trial evaluating an innovative digital resource teaching quality observation of normal child development', Journal of Paediatrics and Child Health, http://dx.doi.org/10.1111/jpc.12485

Heinzen EL; Swoboda KJ; Hitomi Y; Gurrieri F; Bye AM, 2012, 'De novo mutations in ATP1A3 cause alternating hemiplegia of childhood', Nature Genetics, vol. 44, pp. 1030 - 1034, http://dx.doi.org/10.1038/ng.2358

Frizzell C; Connolly AM; Beavis E; Lawson JA; Bye AM, 2010, 'Personalised epilepsy education intervention for adolescents and impact on knowledge acquisition and psychosocial function', Journal of Paediatrics and Child Health (Vol. 48, Suppl. 2, 2012, 1–13), vol. 47, pp. 271 - 275, http://dx.doi.org/10.1111/j.1440-1754.2010.01952.x

Neilson D; Adams M; Orr C; Schelling D; Eiben R; Kerr D; Bassuk A; Bye AM; Childs A; Clarke AR; Crow Y; Di Rocco M; Dohna-Schwake C; Dueckers G; Fasano A; Gika A; Gionnis D; Gorman M; Grattan-Smith PJ; Hackenberg A; Kuster A; Lentschig M; Lopez-Laso E; Marco E; Mastroyianni S; Perrier J; Schmitt-Mechelke T; Servidei S; Skardoutsou A; Uldall P; van der Knaap M; Goglin K; Tefft D; Aubin C; de Jager P; Hafler D; Warman M, 2009, 'Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2', American Journal of Human Genetics, vol. 84, pp. 44 - 51

Bruggemann JM; Wilke M; Som SS; Bye AM; Bleasel AF; Lawson JA, 2009, 'Voxel-based morphometry in the detection of dysplasia and neoplasia in childhood epilepsy: Limitations of grey matter analysis', Journal of Clinical Neuroscience, vol. 16, pp. 780 - 785, http://dx.doi.org/10.1016/j.jocn.2008.08.025

Bye AM; Connolly AM; Farrar MA; Lawson JA; Lonergan A, 2009, 'Teaching paediatric epilepsy to medical students: A randomised crossover trial', Journal of Paediatrics and Child Health (Vol. 48, Suppl. 2, 2012, 1–13), vol. 45, pp. 727 - 730, http://dx.doi.org/10.1111/j.1440-1754.2009.01602.x

Farrar MA; Connolly AM; Lawson JS; Burgess AJ; Lonergan A; Bye AM, 2008, 'Teaching doctors how to diagnose paroxysmal events: a comparison of two educational methods', Medical Education, vol. 42, pp. 909 - 914, http://dx.doi.org/10.1111/j.1365-2923.2008.03146.x

Harkin LA; McMahon JM; Iona X; Dibbens L; Pelekanos JT; Zuberi SM; Sadleir LG; Andermann E; Gill D; Farrell K; Connolly M; Stanley T; Harbord M; Andermann F; Wang J; Batish SD; Jones JG; Seltzer WK; Gardner A; Sutherland G; Berkovic SF; Mulley JC; Scheffer IE; Abbott K; Andrews I; Appleton B; Bleasel A; Buchanan N; Burke C; Bye A; Camfield C; Camfield P; Chow G; Collins K; Cook M; Cross JH; Crow Y; D'Agostino MD; Delatycki M; Dunkley C; Fawke J; Ferrie C; Geraghty M; Graham G; Grattan-Smith P; Hallam E; Hamiwka L; Harding A; Harvey S; Hayman M; Hufton I; Humphries P; Jacob P; Jacquemard R; Jamison D; Jardine P; Jones S; Keene D; Kelley K; Ketteridge D; Kim A; Kivity S; Kneebone C; Kornberg A; Lamb C; Lander C; Lerman-Sagie T; Lev D; Leventer R; Mackay M; Malone S; Manson J; McLellan A; Moore P; Nagarajan L; Nash M; Nikanorova M; Nordli D; O'Regan M; Ouvrier R; Patel J; Pridmore C; Ramesh V; Reutens D; Rowe P; Shield L; Shillito P; Smith L; Spooner C; Wallace G; Watemberg N; Whitehouse W; Wirrell E, 2007, 'The spectrum of SCN1A-related infantile epileptic encephalopathies', Brain, vol. 130, pp. 843 - 852, http://dx.doi.org/10.1093/brain/awm002

Northcott E; Connolly AM; Berroya A; McIntyre J; Christie J; Taylor AJ; Bleasel AF; Lawson JA; Bye AM, 2007, 'Memory and phonological awareness in children with Benign Rolandic Epilepsy compared to a matched control group', Epilepsy Research, vol. 75, pp. 57 - 62, http://dx.doi.org/10.1016/j.eplepsyres.2007.04.004

Bruggemann JM; Wilke M; Som SS; Bye AM; Bleasel AF; Lawson JA, 2007, 'Voxel-based morphometry in the detection of dysplasia and neoplasia in childhood epilepsy: Combined grey/white matter analysis augments detection', Epilepsy Research, vol. 77, pp. 93 - 101, http://dx.doi.org/10.1016/j.eplepsyres.2007.09.004

Bye AM; Connolly AM; Netherton C; Looker PD; Lonergan A; Burgess AJ, 2007, 'A triangulated approach to the assessment of teaching in childhood epilepsy', Medical Teacher, vol. 29, pp. 255 - 257, http://dx.doi.org/10.1080/01421590701287962

Northcott E; Connolly AM; McIntyre J; Christie J; Berroya A; Taylor AJ; Batchelor J; Aaron G; Soe S; Bleasel AF; Lawson JA; Bye AM, 2006, 'Longitudinal assessment of neuropsychologic and language function in children with benign Rolandic epilepsy', Journal of Child Neurology, vol. 21, pp. 518 - 522, http://dx.doi.org/10.2310/7010.2006.00138

Connolly AM; Northcott E; Cairns D; McIntyre J; Christie J; Berroya A; Lawson JA; Bleasel AF; Bye AM, 2006, 'Quality of life of children with benign rolandic epilepsy', Pediatric Neurology, vol. 35, pp. 240 - 245, http://dx.doi.org/10.1016/j.pediatrneurol.2006.03.012

Sabaz M; Lawson JA; Cairns DR; Duchowny MS; Resnick TJ; Dean PM; Bleasel AF; Bye AM, 2006, 'The impact of epilepsy surgery on quality of life in children', Neurology, vol. 66, pp. 557 - 561, http://dx.doi.org/10.1212/01.wnl.0000197788.38783.09

Bye AM; Connolly AM; Netherton C; Looker PD; Burgess AJ; Lonergan A, 2006, 'Learner perceptions of interest, clinical confidence and usefulness in teaching childhood epilepsy', Epilepsia, vol. 47, pp. 128 - 128, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000241385500359&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Connolly AM; Sabaz M; Lawson JA; Cairns DR, 2005, 'Quality of life in childhood epilepsy: Validating the QOLCE', Journal of Paediatrics and Child Health (Vol. 48, Suppl. 2, 2012, 1–13), vol. 41, pp. 157 - 158, http://dx.doi.org/10.1111/j.1440-1754.2005.570_2.x

Berroya A; Bleasel AF; Stevermuer T; Lawson JA; Bye AM, 2005, 'Spike morphology, location, and frequency in benign epilepsy with centrotemporal spikes', Journal of Child Neurology, vol. 20, pp. 188 - 194, http://dx.doi.org/10.1177/08830738050200030401

Northcott E; Connolly AM; Berroya A; Sabaz M; McIntyre J; Christie J; Taylor AJ; Batchelor J; Bleasel AF; Lawson JA; Bye AM, 2005, 'The neuropsychological and language profile of children with benign rolandic epilepsy', Epilepsia, vol. 46, pp. 924 - 930, http://dx.doi.org/10.1111/j.1528-1167.2005.62304.x

Bruggemann JM; Wilke M; Som SS; Bye AM; Bleasel AF; Lawson JA, 2005, 'Voxel based morphometry detects subtle dysplasia and neoplasia in childhood epilepsy', Journal of the Neurological Sciences, vol. 238, pp. S259 - S260, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000235088002249&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Northcott E; Connolly AM; Berroya A; Batchelor J; Taylor AJ; Christie J; McIntyre J; Aron G; Soe S; Bleasel AF; Lawson JA; Bye AM, 2005, 'Neuropsychological and language profile in benign rolandic epilepsy over time', Journal of the Neurological Sciences, vol. 238, pp. S83 - S83, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000235088000317&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Lawson JA; Sabaz M; Cairns DR; Duchowny MS; Resnick TJ; Dean PM; Bleasel AF; Bye AM, 2005, 'The impact of epilepsy surgery on quality of life in children: A prospective study', Epilepsia, vol. 46, pp. 249 - 250, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000232540101117&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Bruggemann JM; Som SS; Lawson JA; Haindi W; Cunningham AM; Bye AM, 2004, 'Application of statistical parametric mapping to SPET in the assessment of intractable childhood epilepsy', European Journal of Nuclear Medicine and Molecular Imaging, vol. 31, pp. 369 - 377, http://dx.doi.org/10.1007/s00259-003-1366-z

Nolan MA; Redoblado M; Lah S; Sabaz M; Lawson JA; Cunningham AM; Bleasel AF; Bye AM, 2004, 'Memory function in childhood epilepsy syndromes', Journal of Paediatrics and Child Health (Vol. 48, Suppl. 2, 2012, 1–13), vol. 40, pp. 20 - 27, http://dx.doi.org/10.1111/j.1440-1754.2004.00284.x

Berroya A; McIntyre J; Webster RI; Lah S; Sabaz M; Lawson JS; Bleasel AF; Bye AM, 2004, 'Speech and language deterioration in benign rolandic', Journal of Child Neurology, vol. 19, pp. 53 - 58, http://dx.doi.org/10.1177/08830738040190010706

Bruggemann JM; Som S; Bye AM; Bleasel AF; Haindl W; Lawson JA, 2004, 'Identification of focal cortical dysplasia and neoplasms in the MRI ofchildren with epilepsy rising voxel based morphometry', Epilepsia, vol. 45, pp. 83 - 83, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000222019500282&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Bye AME; Sabaz M; Gilliam F; Courter P, 2003, 'Validity and clinical relevance of 2 new quality-of-life instruments for children and adults with epilepsy', Advanced Studies in Medicine, vol. 3

Sabaz M; Lawson JA; Cairns DR; Duchowny MS; Resnick TJ; Dean PM; Bye AM, 2003, 'Validation of the Qulaity of Life in Childhood Epilepsy Questionnaire im American epilepsy patients', Epilepsy and Behavior

Nolan MA; Craig ME; Lahra MM; Rawlinson WD; Prager PC; Williams GD; Bye AM; Andrews PI, 2003, 'Survival after pulmonary edema due to enterovirus 71 encephalitis', Neurology, vol. 60, pp. 1651 - 1656, http://dx.doi.org/10.1212/01.WNL.0000066810.62490.FF

Nolan MA; redobaldo MA; Lahz S; Sabaz M; Lawson JA; Cunningham AM; Bleasel AF; Bye AM, 2003, 'Intelligence in childhood epilepsy syndromes', Epilepsy Research, vol. 53, pp. 139 - 150, http://dx.doi.org/10.1016/S0920-1211(02)00261-9

Sabaz M; Lawson JA; Cairns DR; Duchowny MS; Resnick TJ; Dean PM; Bye AM, 2003, 'Validation of the quality of life in childhood epilepsy questionnairein American epilepsy patients', Epilepsy and Behavior, vol. 4, pp. 680 - 691, http://dx.doi.org/10.1016/j.yebeh.2003.08.012

Bye AM, 2003, 'An approach to epilepsy in children and adolescents', Medicine Today, vol. 4, pp. 30 - 36

Sabaz M; Cairns DR; Bleasel AF; Grinton B; Scheffer I; Bye AM, 2003, 'The health-related quality of life of childhood epilepsy syndromes', Journal of Paediatrics and Child Health (Vol. 48, Suppl. 2, 2012, 1–13), vol. 39, pp. 690 - 696, http://dx.doi.org/10.1046/j.1440-1754.2003.00270.x

Lawson JA; Cook MJ; Vogrin S; Litewka L; Strong D; Bleasel AF; Bye AM, 2002, 'Clinical, EEG, and quantitative MRI differences in pediatric frontal and temporal lobe epilepsy', Construction Management and Economics, vol. 58, pp. 723 - 729, http://dx.doi.org/10.1212/WNL.58.5.723

Bye AM; Sabaz ; Cairns DR; Bleasel AF; Lawson JA, 2001, 'The Health Related Quality of Life of Children of Children with Refractory Epilepsy : A Comparison of those with & without Intellectual Disability', Epilepsia, vol. 42, pp. 621 - 628, http://dx.doi.org/10.1046/j.1528-1157.2001.25200.x

Wilmshurst JM; Bye A; Rittey C; Adams C; Hahn AF; Ramsay D; Pamphlett R; Pollard JD; Ouvrier R, 2001, 'Severe infantile axonal neuropathy with respiratory failure.', Muscle Nerve, vol. 24, pp. 760 - 768, http://dx.doi.org/10.1002/mus.1067

Bye AM; Kok DJ; Ferenschild FT; Vyles J, 2000, 'Paroxymal nonepileptic events in children: A retrospective study over a period of ten years', Journal of Paediatrics and Child Health (Vol. 48, Suppl. 2, 2012, 1–13), pp. 244 - 248

Bye AM; Kok DJ; Ferenschild FT; Vles JS, 2000, 'Paroxysmal non-epileptic events in children: A retrospective study over a period of 10 years', Journal of Paediatrics and Child Health (Vol. 48, Suppl. 2, 2012, 1–13), pp. 244 - 248

Lawson JA; Vogrin S; Bleasal AF; Cook B; Bye AM, 2000, 'Cerebral and cerebellar volume reduction in children with intractable epilepsy', Epilepsia, vol. 41, pp. 1456 - 1462, http://dx.doi.org/10.1111/j.1528-1157.2000.tb00122.x

Lawson JA; O Brien T; Bleasal AF; Haindl W; Vogrin S; Cook B; Bye AM, 2000, 'Evaluation of SPECT in the assessment and treatment of intractable childhood epilepsy', Neurology, vol. 55, pp. 1391 - 1393, http://dx.doi.org/10.1212/WNL.55.9.1391

Sabaz ; Cairns DR; Lawson ; Nheu N; Bleasal AF; Bye AM, 2000, 'Validation of a new quality of life measure for children with epilepsy', Epilepsia, vol. 41, pp. 765 - 774, http://dx.doi.org/10.1111/j.1528-1157.2000.tb00240.x

Lawson JA; Vogrin S; Bleasal AF; Cook B; Burns L; Mcanally L; Pereira JK; Bye AM, 2000, 'Predictors of hippocampal, cerebral, and cerebellar volume reduction in childhood epilepsy', Epilepsia, vol. 41, pp. 1540 - 1545, http://dx.doi.org/10.1023/A:1008939132685

Lawson JA; Nguyen W; Bleasel AF; Pereira JK; Vegrin S; Cook M; Bye AM, 1998, 'Ilae-defined Epilepsy syndromes in children: correlation with quantitative MRI', Epilepsia, vol. 39, pp. 1345 - 1349, http://dx.doi.org/10.1111/j.1528-1157.1998.tb01335.x

Lawson JA; Cook MJ; Bleasel AF; Nayanar V; Morris KF; Bye AME, 1997, 'Quantitative MRI in outpatient childhood epilepsy', Epilepsia, vol. 38, pp. 1289 - 1293, http://dx.doi.org/10.1111/j.1528-1157.1997.tb00066.x

Bye AM; Cook M; Moore KJ; Bleasel AF; Nayanar V, 1997, 'QUANTITATIVE MRI STUDIES IN CHILDHOOD EPILEPSY', INTERNATIONAL LEAGUE AGAINST EPILEPSY, pp. 1289 - 1293

Bye AM; Lee DJ; Naidoo D; Flanagan D, 1997, 'The effects of morphine and midazolam on EEGs in neonates', Journal of Neuropsychiatry and Clinical Neurosciences, pp. 173 - 175

Cunningham CA; Bye AM; Flanagan D; Cheek K, 1997, 'OUTCOME OF NEONATES WITH ELECTROGRAPHICALLY IDENTIFIED SEIZURES, OR AT RISK OF SEIZURES', Pediatric Neurology, vol. 16, pp. 225 - 231

Bye AM; Gotmj ; Flanagan D; Roseb ; Mizre , 1997, 'EVALUATION OF AN AUTOMATIC SEIZURE DETECTION METHOD FOR THE NEWBORN EEG', Journal of Clinical Neuroscience, vol. 103, pp. 363 - 369

Bye AM, 1997, 'THE EFFECTS OFMORPHINE AND MIDAZOLAM ON EEGS IN NEONATES', Journal of Clinical Neuroscience, pp. 173 - 175

Flanagan D; Gotman J; Rosenblatt B; Bye A; Mizrahi EM, 1997, 'MULTI-CENTER VALIDATION OF AUTOMATED SEIZURE DETECTION IN THE NEWBORN', Journal of Clinical Neurophysiology, vol. 14, pp. 162 - 162, http://dx.doi.org/10.1097/00004691-199703000-00036

Bye AM; Flanagan D, 1995, 'Spatial and temporal characteristics of neonatal seizures', Epilepsia, pp. 1009 - 1016

Bye AM; Flanagan D, 1995, 'Electroencephalograms clinical observations and the monitoring of neonatal seizures', Journal of Paediatrics and Child Health (Vol. 48, Suppl. 2, 2012, 1–13), pp. 503 - 507

O Meara M; Bye AM; Flanagan D, 1995, 'Clinical features of neonatal seizures', Journal of Paediatrics and Child Health (Vol. 48, Suppl. 2, 2012, 1–13), pp. 237 - 240

Fletcher JM; Bye AM; Nayanar V; Wilcken B, 1995, 'Non-ketotic hyperglycinaemia presenting as pachygyria.', J Inherit Metab Dis, vol. 18, pp. 665 - 668, http://dx.doi.org/10.1007/BF02436754

Bye AME; Foo S, 1994, 'Complex Partial Seizures in Young Children', Epilepsia, vol. 35, pp. 482 - 488, http://dx.doi.org/10.1111/j.1528-1157.1994.tb02466.x

Bye AM, 1994, 'Neonate with benign familial neonatal convulsions: recorded generalized and focal seizures.', Pediatr Neurol, vol. 10, pp. 164 - 165, http://dx.doi.org/10.1016/0887-8994(94)90052-3

CHEE KY; LEE D; BYRON D; NAIDOO D; BYE A, 1993, 'A SIMPLE COLLECTION METHOD FOR SALIVA IN CHILDREN - POTENTIAL FOR HOME MONITORING OF CARBAMAZEPINE THERAPY', BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, vol. 35, pp. 311 - 313, http://dx.doi.org/10.1111/j.1365-2125.1993.tb05700.x

Bye AM; Parle J; Haindl W, 1993, 'Single photon emission computed tomography in intractable infantile seizures.', Clinical and experimental neurology, vol. 30, pp. 117 - 126

Reutens DC; Bye AM; Hopkins IJ; Banks A; Somerville E; Walsh J; Bleasel A; Ouvrier R; MacKenzie RA; Manson JI; Bladin PF; Berkovic SF, 1993, 'Corpus Callosotomy for Intractable Epilepsy: Seizure Outcome and Prognostic Factors', Epilepsia, vol. 34, pp. 904 - 909, http://dx.doi.org/10.1111/j.1528-1157.1993.tb02110.x

Bye AM; Nunan J, 1992, 'Video EEG analysis of non-ictal events in children.', Clin Exp Neurol, vol. 29, pp. 92 - 98, https://www.ncbi.nlm.nih.gov/pubmed/1343877

Bye A; Lamont P; Healy L, 1990, 'Commencement of a paediatric EEG-video telemetry service.', Clin Exp Neurol, vol. 27, pp. 83 - 88, https://www.ncbi.nlm.nih.gov/pubmed/2129962

Bye AM; Baker WD; Pollard J; Wise G, 1990, 'Hereditary sensory neuropathy type II without trophic changes.', Dev Med Child Neurol, vol. 32, pp. 164 - 171, http://dx.doi.org/10.1111/j.1469-8749.1990.tb16915.x

Bye AM; Matheson JM; Tobias VH; Mackenzie RA, 1989, 'Selective epilepsy surgery in tuberous sclerosis.', Aust Paediatr J, vol. 25, pp. 243 - 245, http://dx.doi.org/10.1111/j.1440-1754.1989.tb01465.x

Bye AM; Matheson JM; Mackenzie RA, 1989, 'Epilepsy surgery in Sturge-Weber syndrome.', Aust Paediatr J, vol. 25, pp. 103 - 105, http://dx.doi.org/10.1111/j.1440-1754.1989.tb01428.x

Bye AM; Vines R; Fronzek K, 1983, 'The obesity hypoventilation syndrome and the Prader-Willi syndrome.', Aust Paediatr J, vol. 19, pp. 251 - 255, http://dx.doi.org/10.1111/j.1440-1754.1983.tb02114.x

Conference Papers

Kandula T; Teoh HL; Andrews I; Bye A; Farrar MA, 2014, 'Enterovirus 71 associated lower motor neuron disease in infants and children', Amsterdam, The Netherlands, presented at 13th International Child Neurology Congress, Amsterdam, The Netherlands

Smee RI; Cohn R; Ziegler D; Kwok B; Johnston H; Bye A; Andrews I; Stening W, 2010, 'A RETROSPECTIVE REVIEW OF CHILDREN TREATED AT THE SYDNEY CHILDREN'S HOSPITAL/PRINCE OF WALES HOSPITAL', in NEURO-ONCOLOGY, OXFORD UNIV PRESS INC, AUSTRIA, Vienna, pp. II69 - II70, presented at 14th International Symposium on Pediatric Neuro-Oncology, AUSTRIA, Vienna, 20 June 2010 - 23 June 2010, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000278817700314&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Connolly AM; Northcott E; Cairns DR; McIntyre J; Christie J; Berroya A; Lawson JA; Bleasel AF; Bye AME, 2005, 'Quality of life of children with Benign Rolandic Epilepsy', in JOURNAL OF THE NEUROLOGICAL SCIENCES, ELSEVIER, AUSTRALIA, Sydney, pp. S119 - S119, presented at 18th World Congress of Neurology, AUSTRALIA, Sydney, 05 November 2005 - 11 November 2005, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000235088001096&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Randall RB; Bye AM; Gao Y, 1998, 'Bearing diagnostics by digital analysis techniques in high background noise situations', in Sas P (ed.), International Conference on Noise and Vibration Engineering 1998, International Conference on Noise and Vibration Engineering 1998, Leuven, Belgium, pp. 1379 - 1386, presented at International Conference on Noise and Vibration Engineering 1998, Leuven, Belgium, 16 September 1998 - 18 September 1998

Conference Posters

Ng E; Le Marne F; Sinclair K; Lorentzos M; Waak M; Deuble N; Georgeson T; Rao A; Rikhi S; Bye A, 2019, 'The evaluation of an educational video counselling key messages for doctors and families following a first afebrile seizure', presented at Epilepsy Society of Australia 30th Annual Scientific Meeting, 6th – 8th November 2019, 06 November 2019 - 08 November 2019

Macintosh R; Nevin S; Le Marne F; McGill B; Sachdev R; Wakefield C; Bye A; Palmer E, 2019, 'Co-development of education and support resources for families with severe early-onset genetic epilepsy', Welcome Genome Campus, UK, presented at World Congress of Genetic Counselling, Welcome Genome Campus, UK, 02 October 2019 - 04 October 2019

Le Marne F; Butler S; Beavis E; O'Brien AM; Gill D; Bye A, 2017, 'Design and development of a novel App for adolescents with epilepsy', Perth, presented at Epilepsy Society of Australia 31st Annual Scientific Meeting, Perth, 01 November 2017 - 03 November 2017

Le Marne F; McGinness H; Slade R; Cardamone M; Balbir Singh S; Bye A, 2015, 'The first unprovoked seizure: validation of a newly developed e-learning resource', Adelaide, South Australia, presented at Epilepsy Society of Australia 29th Annual Scientific Meeting, Adelaide, South Australia, 21 October 2015 - 23 October 2015

Johnson AM; Sugo E; Barreto D; Hiew C; Lawson J; Connolly A; Somerville E; Hasic E; Cunningham AM; Bye AME, 2013, 'Does the severity of gliosis in hippocampal sclerosis correlate with epilepsy burden and predict outcome after temporal lobectomy?', in Does the severity of gliosis in hippocampal sclerosis correlate with epilepsy burden and predict outcome after temporal lobectomy?, Epilepsy Society of Australia, Sydney, Australia, presented at Epilepsy Society of Australia, Sydney, Australia, 01 November 2013 - 04 November 2013

Conference Presentations

Nevin S; Wakefield C; Le Marne F; Beavis E; Macintosh R; Sachdev R; Bye A; Palmer E; Nunn K, 2021, 'Evaluating positive psychology resources among caregivers of a child with a genetic epilepsy', Held virtually, presented at The Australian and New Zealand Child Neurology Society (ANZCNZ) 9th Annual Scientific Meeting, Held virtually, 13 September 2021 - 15 September 2021

Le Marne F; Butler S; Beavis E; O'Brien AM; Gill D; Bye A, 2017, 'Design, development and evaluation of an app for adolescents with epilepsy', Brisbane, QLD, presented at The Australian and New Zealand Child Neurology Society 6th Annual Scientific Meeting, Brisbane, QLD, 09 August 2017 - 11 August 2017

McGinness H; Le Marne FA; Slade R; Cardamone M; Bye A, 2015, 'The first unprovoked seizure: validation of a newly developed e-learning resource.', Melbourne, Australia, presented at The Australian and New Zealand Child Neurology Society 4th Annual Scientific Meeting, Melbourne, Australia, 26 August 2015 - 28 August 2015

McGinness H; Le Marne F; Slade R; Cardamone M; Bye A, 2015, 'The first unprovoked seizure: validation of a newly developed e-learning resource', Melbourne, Australia, presented at The Australian and New Zealand Child Neurology Society 4th Annual Scientific Meeting, Melbourne, Australia, 26 August 2015 - 26 August 2015

Conference Abstracts

Johnson A; Bye A; Ziegler D; Gifford A; Jacobsen E; Cohn R, 2018, 'CRAN-27. PAEDIATRIC EXTRAVENTRICULAR NEUROCYTOMA: A SERIES AND A RARE COMPLICATION', in Neuro-Oncology, Oxford University Press (OUP), Vol. 20, pp. i42 - i42, http://dx.doi.org/10.1093/neuonc/noy059.063

Carvill GL; Heavin SB; Yendle SC; O'Roak BJ; Cook J; Khan A; Dorschner MO; Weaver MA; Calvert S; Malone S; Wallace G; Stanley T; Bye AM; Bleasel A; Howell KB; Kivity S; Mackay MT; Rodriguez-Casero V; Webster R; Korczyn A; Zelnick N; Lerman-Sagie T; Lev D; Moller SR; Andrade DM; Freeman JL; Sadleir LG; Shendure J; Berkovic SF; Scheffer IE; Mefford HC, 2013, 'TARGETED RESEQUENCING IN EPILEPTIC ENCEPHALOPATHIES REVEALS MARKED GENETIC HETEROGENEITY AND NOVEL GENES', in EPILEPSIA, WILEY-BLACKWELL, CANADA, Montreal, Vol. 54, pp. 16 - 16, presented at 30th International Epilepsy Congress, CANADA, Montreal, 23 June 2013 - 27 June 2013, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000320472000037&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Johnson AM; Boyle R; Connolly A; Lloyd O; Lawson J; Bye AME, 2012, 'Change in cognitive functioning after paediatric temporal lobectomy', in Developmental Medicine and Child Neurology, Wiley, Brisbane, Australia, presented at International Child Neurology Congress, Brisbane, Australia

Other

Palmer EE; Hong S; Al Zahrani F; Hashem MO; Aleisa FA; Jalal Ahmed HM; Kandula T; Macintosh R; Minoche AE; Puttick C; Gayevskiy V; Drew AP; Cowley MJ; Dinger M; Rosenfeld JA; Xiao R; Cho MT; Yakubu SF; Henderson LB; Guillen Sacoto MJ; Begtrup A; Hamad M; Shinawi M; Andrews MV; Jones MC; Lindstrom K; Bristol RE; Kayani S; Snyder M; Villanueva MM; Schteinschnaider A; Faivre L; Thauvin C; Vitobello A; Roscioli T; Kirk EP; Bye A; Merzaban J; Jaremko Ł; Jaremko M; Sachdev RK; Alkuraya FS; Arold ST, 2019, Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013)), http://dx.doi.org/10.1016/j.ajhg.2019.03.016

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