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PROF SAM BERKOVIC



Contact Details

Organization: Medicine - Austin Health and Northern Health
Position: AUSTRALIA FELLOW
Email:
Work: 9496 2330
Mobile: 0408 325 969
Fax: 9496 2291
Level: 01
Building: No Building
Campus: Repatriation Hospital

Research Expertise and International Linkages

Research Expertise

Research Interest Key Words Country of Expertise
Epilepsy Seizures, ion channels Australia, Israel, Canada
Sleep disorders Narcolepsy, Parasomnias Australia
Neurogenetics Linkage analysis, ion channels Australia, Israel, Canada

Qualifications, Honours, Fellowships and Other Awards

Qualifications

Title Institution Date Awarded Abbreviation
Bachelor of Medical Science University of Melbourne 17-Dec-1977
Bachelor of Medicine and Bachelor of Surgery University of Melbourne 17-Dec-1977
Doctor of Medicine University of Melbourne 01-Jan-1985

Memberships

Membership Type Membership Body Description Start Date End Date
Member Epilepsy Society of Australia Full Member 01-Jan-1988
Member Australian Association of Neurologists Full Member 01-Jan-1981
Associate American Academy of Neurology Associate Clinical Member 01-Jan-1990
Member American Epilepsy Society Corresponding Member 01-Jan-1994
Member American Neurological Association Corresponding Member 01-Jan-2004

Honours

Honour Date Awarded
Member of the Order of Australia 2005

Fellowships

Fellowship Date Awarded
Fellow of the Royal Australasian College of Physicians (FRACP) 06-Jan-1984
Fellow of the Australian Academy of Science (FAA) 24-Mar-2005
Fellow of the Royal Society (FRS) 17-May-2007

Government Research Classifications

Research Fields, Courses and Discipline Classifications

Socio-Economic Objective Classifications

Grants and Contracts

Research Grants, Contracts and Consultancies awarded to the University of Melbourne as the administering institution (since 2003) as recorded in Themis Agreements.

Grants

Title Role Funding Source Scheme Award Date
CCRE Program - Neurosciences: Cross-Discipline Enhancement of Clinical Research and Education Chief Investigator NHMRC Centres of Clinical Research Excellence (CCRE) 01/01/2003
Epilepsy: A collaborative research program from genome to patient Chief Investigator NHMRC Program Grants 01/01/2003
Predicting the evolution of psychosocial and cognitive difficulties in epilepsy: a preventive approach Chief Investigator AUST RESEARCH COUNCIL,
GLAXOSMITHKLINE AUSTRALIA
Linkage Projects (AUST RESEARCH COUNCIL) 01/01/2004
Epilepsy: Molecular basis and mechanisms in the era of functional genomics Chief Investigator NHMRC Program Grants 01/01/2006
EPILEPSY RESEARCH Chief Investigator JOHN T REID CHARITABLE TRUSTS Research Grant 24/08/2006
NHMRC Australia Fellowship Chief Investigator NHMRC Australia Fellowship 01/01/2007
PHOTOSENSITIVITY AS AN EPILEPSY ENDOPHENOTYPE: A SUB STUDY OF GENETICS OF HUMAN EPILEPSY Principal Supervisor NHMRC Medical & Dental Postgraduate Scholarships 01/01/2007
Novel molecular and bioinformatic approaches facilitate epilepsy gene discovery Chief Investigator AMERICAN EPILEPSY SOCIETY Research Initiative Awards 19/01/2007
An international strategy for gene identification leading to discovery of new targets for treatment of neurological disease Chief Investigator DEPT OF INNOVATION INDUSTRY SCIENCE & RESEARCH,
DEPT OF EDUCATION SCIENCE & TRAINING
International Science Linkages (DEPT OF EDUCATION SCIENCE & TRAINING) 31/08/2007
GENETICS OF EPILEPSY: THE TESTIMONY OF TWINS Chief Investigator PFIZER AUST PTY LTD Neuro Science Research Grants 12/11/2007
Finding Genes for Familial Fainting Chief Investigator NHMRC Project Grants 01/01/2008
Improved access to a clinical research educational program for healthcare practitioners and professionals Chief Investigator ELI LILLY AUST PTY LTD Research Grants 01/01/2009
Genetic basis of the epilepsies Chief Investigator THYNE REID FOUNDATION Research Grants 01/06/2009

Publications

Publications produced at the University of Melbourne and reported in the Annual Publications Collection and 'Research Report' since 2001. The Themis Publications module, released in November 2006, allows additional publications from previous institutions and publications from past years to be entered.

Publications in 2009

Journal Articles

  • Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+?


    Year: 2009
    Journal: Epilepsia
    Volume: 50
    Issue: 4
    Page numbers: 953-956
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  • Why do seizures in generalized epilepsy often occur in the morning?


    Year: 2009
    Journal: Neurology
    Volume: 73
    Page numbers: 218-222
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  • A neurologist's guide to genome-wide association studies
    Year: 2009
    Journal: Neurology
    Volume: 72
    Page numbers: 558-565
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  • Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1
    Year: 2009
    Journal: Annals of Neurology
    Volume: 66
    Issue: 3
    Page numbers: 415-419
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  • Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance
    Year: 2009
    Journal: Human Molecular Genetics
    Volume: 18
    Issue: 19
    Page numbers: 3626-3631
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  • Multidrug-resistant genotype (ABCB1) and seizure recurrence in newly treated epilepsy: Data from International Pharmacogenetic Cohorts
    Year: 2009
    Journal: Epilepsia
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  • Personality development in the context of intractable epilepsy
    Year: 2009
    Journal: Archives of Neurology
    Volume: 66
    Issue: 1
    Page numbers: 68-72
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  • The peri-ictal state:  cortical excitability changes within 24h of a seizure
    Year: 2009
    Journal: Brain
    Volume: 132
    Page numbers: 1013-1021
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  • The role of neuronal GABAA receptor subunit mutations in idiopathic generalized epilepsies
    Year: 2009
    Journal: Neuroscience Letters
    Volume: 453
    Page numbers: 162-165
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Publications in 2008

Journal Articles

  • Generalized epilepsy with febrile seizures plus A genetic disorder with heterogeneous clinical phenotypes


    Year: 2008
    Journal: Brain
    Volume: 120
    Page numbers: 479-490
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  • Obstetric events as a risk factor for febrile seizures: A community-based twin study


    Year: 2008
    Journal: Twin Research and Human Genetics
    Volume: 11
    Issue: 6
    Page numbers: 634-640
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  • Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1


    Year: 2008
    Journal: Brain
    Volume: 131
    Page numbers: 1831-1844
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  • The human variome project


    Year: 2008
    Journal: Science
    Volume: 322
    Page numbers: 861-862
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  • X-linked protocadherin 19 mutations cause femalelimited epilepsy and cognitive impairment


    Year: 2008
    Journal: Nature Genetics
    Volume: 40
    Issue: 6
    Page numbers: 776-781
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  • A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome
    Year: 2008
    Journal: American Journal of Human Genetics
    Volume: 83
    Page numbers: 572-581
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  • Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis
    Year: 2008
    Journal: American Journal of Human Genetics
    Volume: 82
    Issue: 2008
    Page numbers: 673-684
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  • Association of a Nicotinic Receptor Mutation with Reduced Height and Blunted Physostigmine-Stimulated Growth Hormone Release
    Year: 2008
    Journal: Journal of Clinical Endocrinology & Metabolism
    Volume: 93
    Issue: 2
    Page numbers: 634-637
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  • Benign occipital epilepsies of childhood: clinical features and genetics
    Year: 2008
    Journal: Brain
    Volume: 131
    Page numbers: 2287-2294
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  • Cognitive complaints after a first seizure in adulthood: Influence of psychological adjustment
    Year: 2008
    Journal: Epilepsia
    Volume: 49
    Issue: 11
    Page numbers: 1-10
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  • Developmental Impact of a Famial GABA A Receptor Epilepsy Mutation
    Year: 2008
    Journal: Annals of Neurology
    Volume: 64
    Page numbers: 284-293
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  • Epilepsy and mental retardation limited to females: an under-recognized disorder
    Year: 2008
    Journal: Brain
    Volume: 131
    Page numbers: 918-927
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  • Gene expression analysis in absence epilepsy using a monozygotic twin design
    Year: 2008
    Journal: Epilepsia
    Volume: 49
    Issue: 9
    Page numbers: 1546-1554
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  • Human Nocturnal Frontal Lobe Epilepsy: Pharmocogenomic Profiles of Pathogenic Nicotinic Acetylcholine Receptor B-Subunit Mutations outside the Ion Channel Pore
    Year: 2008
    Journal: Molecular Pharmacology
    Volume: 74
    Issue: 2008
    Page numbers: 379-391
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  • Intracortical hyperexcitability inhumans with GABAA receptor mutation
    Year: 2008
    Journal: Cerebral Cortex
    Volume: 18
    Page numbers: 664-669
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  • Mechanisms of human inherited epilepsies
    Year: 2008
    Journal: Progress in Neurobiology
    Volume: 87
    Page numbers: 41-57
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  • Multifocal epilepsy: the role of palliative resection - intractable frontal and occipital lobe epilepsy secondary to radiotherapy for acute lymphoblastic leukaemia
    Year: 2008
    Journal: Epileptic Disorders
    Volume: 10
    Issue: 4
    Page numbers: 362-70
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  • Navigating the channels and beyond: unravelling the genetics of the epilepsies
    Year: 2008
    Journal: The Lancet Neurology
    Volume: 7
    Issue: 2008
    Page numbers: 231-245
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  • Reduced striatal D1 receptor binding in autosomal dominant noctural frontal lobe epilepsy
    Year: 2008
    Journal: Neurology
    Volume: 71
    Page numbers: 795-798
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  • SOMATIC MUTATIONS IN GLI3 CAN CAUSE HYPOTHALAMIC HAMARTOMA AND GELASTIC SEIZURES
    Year: 2008
    Journal: Neurology
    Volume: 70
    Issue: 8
    Page numbers: 653-655
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  • Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability
    Year: 2008
    Journal: Epilepsia
    Volume: 49
    Issue: 5
    Page numbers: 2125-2129
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Publications in 2007

Book Chapters

  • Generalized (genetic) epilepsy with febrile seizures plus


    Year: 2007
    Book: Epilepsy: A comprehensive textbook
    Publisher: Lippincott Williams & Wilkins(Philadelphia)
    Authors(s):
    Editors(s):
  • Genetic Epilepsies
    Year: 2007
    Book: Molecular Neurology
    Publisher: Elsevier Science
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Journal Articles

  • Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy


    Year: 2007
    Journal: Epilepsy Research
    Volume: 76
    Issue: 1
    Page numbers: 41-48
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  • Adjunctive therapy of uncontrolled partial seizures with levetiracetam in Australian patients


    Year: 2007
    Journal: Epilepsy and Behavior
    Volume: 11
    Issue: 2007
    Page numbers: 338-342
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  • Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants


    Year: 2007
    Journal: Annals of Neurology
    Volume: 62
    Issue: 6
    Page numbers: 560-568
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  • GEFS+ where focal seizures evolve from generalized spike wave: video-EEG study of two children


    Year: 2007
    Journal: Epileptic Disorders
    Volume: 9
    Issue: 3
    Page numbers: 307-314
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  • Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy


    Year: 2007
    Journal: Proceedings of the National Academy of Sciences of the United States of America
    Volume: 104
    Issue: 44
    Page numbers: 17536-17541
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  • The spectrum of SCN1A-related infantile epileptic encephalopathies


    Year: 2007
    Journal: Brain
    Volume: 130
    Issue: pt 3
    Page numbers: 843-852
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  • A Multicenter Study of BRD2 as a Risk Factor for Juvenile Myoclonic Epilepsy
    Year: 2007
    Journal: Epilepsia
    Volume: 48
    Issue: 4
    Page numbers: 706-712
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  • A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channel
    Year: 2007
    Journal: Molecular and Cellular Neurosciences
    Volume: 35
    Issue: 2
    Page numbers: 292-301
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  • Association studies and functional validation or functional validation alone?


    Year: 2007
    Journal: Epilepsy Research
    Volume: 74
    Issue: 2-3
    Page numbers: 237-238
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  • Changes in cortical excitability differentiate generalized and focal epilepsy
    Year: 2007
    Journal: Annals of Neurology
    Volume: 61
    Issue: 4
    Page numbers: 324-331
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  • Channelopathies in Idiopathic Epilepsy


    Year: 2007
    Journal: Neurotherapeutics
    Volume: 4
    Issue: 2
    Page numbers: 295-304
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  • Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures

    Year: 2007
    Journal: Journal of Medical Genetics
    Volume: 44
    Issue: 12
    Page numbers: 791-796
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  • Founder Effect with Variable Age at Onset in Arab Families with Lafora Disease and EPM2A Mutation

    Year: 2007
    Journal: Epilepsia
    Volume: 48
    Issue: 5
    Page numbers: 1011-1014
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  • Generalized epilepsy with febrile seizures plus-associated sodium channel beta1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function
    Year: 2007
    Journal: Neuroscience
    Volume: 148
    Issue: 1
    Page numbers: 164-174
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  • Hippocampal Sclerosis: MR Prediction of Seizure Intractability
    Year: 2007
    Journal: Epilepsia
    Volume: 48
    Issue: 2007
    Page numbers: 315-323
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  • Impaired verbal associative learning after resection of left perirhinal cortex
    Year: 2007
    Journal: Brain
    Volume: April
    Issue: 2007
    Page numbers: 1423-1431
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  • Intracortical Hyperexcitability in Humans with a GABAA Receptor Mutation

    Year: 2007
    Journal: Cerebral Cortex
    Volume: July
    Issue: 2007
    Page numbers: 397-405
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  • Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

    Year: 2007
    Journal: Epilepsia
    Volume: 48
    Issue: 9
    Page numbers: 1807-1809
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  • Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
    Year: 2007
    Journal: The Lancet Neurology
    Volume: 6
    Issue: 11
    Page numbers: 970-980
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  • Nicotine-Induced Dystonic Arousal Complex in a Mouse Line Harboring a Human Autosomal-Dominant Nocturnal Frontal Lobe Epilepsy Mutation
    Year: 2007
    Journal: Neuroscience
    Volume: 27
    Issue: 38
    Page numbers: 10128-10142
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  • Placebo-controlled study of levetiracetam in idiopathic generalized epilepsy
    Year: 2007
    Journal: Neurology
    Volume: 69
    Issue: 2007
    Page numbers: 1751-1760
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  • Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines

    Year: 2007
    Journal: Human Molecular Genetics
    Volume: 16
    Issue: 4
    Page numbers: 364-373
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  • SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum
    Year: 2007
    Journal: Epilepsia
    Volume: 48
    Issue: 6
    Page numbers: 1138-1142
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  • Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations
    Year: 2007
    Journal: Brain
    Volume: 130
    Issue: 2007
    Page numbers: 100-109
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  • The psychological impact of a newly diagnosed seizure: Losing and restoring perceived control


    Year: 2007
    Journal: Epilepsy and Behavior
    Volume: 10
    Issue: 2
    Page numbers: 223-233
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  • Vaccination, seizures and 'vaccine damage'
    Year: 2007
    Journal: Current Opinion in Neurology
    Volume: 20
    Issue: 2
    Page numbers: 181-187
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Publications in 2006

Book Chapters

  • Genetics of Epilepsy: Principles and practice
    Year: 2006
    Book: Pediatric Neurology: Principles & Practice
    Publisher: Mosby International(St Louis)
    Authors(s):
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Journal Articles

  • SRPX2 mutations in disorders of language cortex and cognition
    Year: 2006
    Journal: Human Molecular Genetics
    Volume: 15
    Issue: 2006
    Page numbers: 1195-1207
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  • Update on pharmacogenetics in epilepsy: a brief review.


    Year: 2006
    Journal: The Lancet Neurology
    Volume: 5
    Page numbers: 189-196
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  • A GABAA receptor mutation causing generalized eilepsy reduces benzodiazepine receptor binding
    Year: 2006
    Journal: Neuroimage
    Volume: 32
    Issue: 2006
    Page numbers: 995-1000
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  • A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A
    Year: 2006
    Journal: Neurology
    Volume: 67
    Issue: 2006
    Page numbers: 1094-1095
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  • A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A
    Year: 2006
    Journal: Neurology
    Volume: 67
    Issue: 2006
    Page numbers: 2224-2226
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  • Action myoclonus-renal failure syndrome: a cause for worsening tremor in young adults
    Year: 2006
    Journal: Neurology
    Volume: 67
    Issue: 2006
    Page numbers: 1310-1311
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  • Analyzing the etiology of Benign rolandic epilepsy: A multicenter twin collaboration
    Year: 2006
    Journal: Epilepsia
    Volume: 47
    Issue: 3
    Page numbers: 550-555
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  • Analyzing the etiology of benign rolandic epilepsy: a multicentre twin collaboration
    Year: 2006
    Journal: Epilepsia
    Volume: 47
    Issue: 3
    Page numbers: 550-555
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  • Are epilepsy classifications based on epileptic syndromes and seizure types outdated?
    Year: 2006
    Journal: Epileptic Disorders
    Volume: 8
    Issue: 2006
    Page numbers: 159-160
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  • De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study
    Year: 2006
    Journal: The Lancet Neurology
    Volume: 5
    Issue: 2006
    Page numbers: 488-492
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  • Exploration of the Genetic Architecture of Idiopathic Generalized Epilepsies
    Year: 2006
    Journal: Epilepsia
    Volume: 47
    Issue: 2006
    Page numbers: 1682-1690
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  • Febrile seizures: traffic slows in the heat
    Year: 2006
    Journal: Trends in Molecular Medicine
    Volume: 12
    Issue: 2006
    Page numbers: 343-344
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  • Human epilepsies: interaction of genetic and acquired factors
    Year: 2006
    Journal: Trends in Neurosciences
    Volume: 29
    Issue: 2006
    Page numbers: 391-397
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  • Increased serotonin receptor availability in human sleep: Evidence from an [18F]MPPF PET study in narcolepsy
    Year: 2006
    Journal: Neuroimage
    Volume: 30
    Issue: 2006
    Page numbers: 341-348
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  • Invited comments on the Shostak and Ottman review. Genetic research on the epilepsies.
    Year: 2006
    Journal: Epilepsia
    Volume: 47
    Issue: 2006
    Page numbers: 1751-1752
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  • New-onset temporal lobe epilepsy in children: Lesion on MRI predicts poor seizure outcome
    Year: 2006
    Journal: Neurology
    Volume: 67
    Issue: 2006
    Page numbers: 2147-2153
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  • Paroxysmal Motor Disorders of Sleep: The Clinical Spectrum and Differentiation from Epilepsy
    Year: 2006
    Journal: Epilepsia
    Volume: 47
    Issue: 2006
    Page numbers: 1775-1791
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  • Prediction of drug resistance in epilepsy: not as easy as ABC
    Year: 2006
    Journal: Neurology
    Volume: 5
    Issue: 2006
    Page numbers: 641-642
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  • Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adults
    Year: 2006
    Journal: Neurology
    Volume: 67
    Issue: 2006
    Page numbers: 2224-2226
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  • Sleep deprivation increases cortical excitability in epilepsy. Syndrome specific effects.
    Year: 2006
    Journal: Neurology
    Volume: 67
    Issue: 2006
    Page numbers: 1018-1022
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  • What happens now? Ongoing outcome after post-temproal lobectomy seizure recurrence
    Year: 2006
    Journal: Neurology
    Volume: 67
    Issue: 2006
    Page numbers: 1671-1673
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Publications in 2005

Book Chapters

  • Introduction to Epilepsy
    Year: 2005
    Book: Magnetic Resonance in Epilepsy
    Publisher: Academic Press - Elsevier Science(Burlington)
    Authors(s):

Journal Articles

  • A new clinical and molecular form of Uverricht-Lundborg disease localized by homozygosity mapping
    Year: 2005
    Journal: Brain
    Volume: 128
    Page numbers: 652-658
    Publisher: Oxford University Press(Oxford)
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  • An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures
    Year: 2005
    Journal: Neurology
    Volume: 64
    Page numbers: 142-144
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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  • Assessment of the role of FDG PET in the diagnosis and management of children with refractory epilepsy
    Year: 2005
    Journal: European Journal of Nuclear Medicine and Molecular Imaging
    Volume: 32
    Page numbers: 1311-1316
    Publisher: Springer Verlag
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  • Early seizures after temporal lobectomy predict subsequent seizure recurrence
    Year: 2005
    Journal: Annals of Neurology
    Volume: 57
    Issue: 2
    Page numbers: 283-288
    Publisher: Wiley-Liss(New York)
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  • Effect of antiepileptic medication on bone mineral measures
    Year: 2005
    Journal: Neurology
    Volume: 65
    Page numbers: 1358-1363
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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  • Efficacy and safety of levetiracetam 1000-3000 mg/day in patients with refractory partial-onset seizures: a multicenter, open-label single-arm study
    Year: 2005
    Journal: Epilepsy Research
    Volume: 63
    Page numbers: 1-9
    Publisher: Elsevier Science(Amsterdam)
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  • Familial clustering of seizure types within the idiopathic generalized epilepsies
    Year: 2005
    Journal: Neurology
    Volume: 65
    Page numbers: 523-528
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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  • Increased serotonin receptor availability in human sleep: Evidence from an [18F]MPPF PET study in narcolepsy
    Year: 2005
    Journal: Neuroimage
    Volume: 30
    Issue: 2
    Page numbers: 1-8
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  • Is variation in the GABA(B) Receptor 1 Gene Associated with Temporal Lobe Epilepsy?
    Year: 2005
    Journal: Epilepsia
    Volume: 46
    Issue: 5
    Page numbers: 778-780
    Publisher: Blackwell Science(Massachusetts)
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  • Mutation in the Na+ channel subunit SCN I B produces paradoxical changes in peripheral nerve excitability
    Year: 2005
    Journal: Brain
    Volume: 128
    Issue: 8
    Page numbers: 1841-1846
    Publisher: Oxford University Press(Oxford)
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  • Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+)
    Year: 2005
    Journal: Epilepsia
    Volume: 46
    Issue: supp 10
    Page numbers: 41-47
    Publisher: Blackwell Science(Massachusetts)
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  • Reply: Genetic influence on rolandic epilepsy
    Year: 2005
    Journal: Annals of Neurology
    Volume: 57
    Issue: 3
    Page numbers: 465
    Publisher: Wiley-Liss(New York)
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  • SCN1A Mutations and Epilepsy
    Year: 2005
    Journal: Human Mutation
    Volume: 25
    Page numbers: 535-542
    Publisher: Wiley-Liss(New York)
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  • Susceptibility genes for complex epilepsy
    Year: 2005
    Journal: Human Molecular Genetics
    Volume: 14
    Issue: 2
    Page numbers: R243-R249
    Publisher: Oxford University Press(Oxford)
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  • Tramadol and new-onset seizures
    Year: 2005
    Journal: Medical Journal of Australia
    Volume: 182
    Issue: 1
    Page numbers: 42-43
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  • Treatment of new-onset epilepsy: seizures beget discussion
    Year: 2005
    Journal: The Lancet
    Volume: 365
    Issue: 11 June 2005
    Page numbers: 1985-1986
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  • Treatment with anti-epileptic drugs
    Year: 2005
    Journal: Australian Family Physician
    Volume: 34
    Issue: 12
    Page numbers: 1017-1020
    Publisher: Royal Australian College of General Practitioners
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Publications in 2004

Journal Articles

  • Endozepine stupor: disease or deception? A critical review


    Year: 2004
    Journal: Sleep
    Volume: 27
    Issue: 8
    Page numbers: 1597-1599
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  • Sandifer syndrome misdiagnosed as refractory partial seizures in an adult


    Year: 2004
    Journal: Epileptic Disorders
    Volume: 6
    Issue: 2004
    Page numbers: 49-50
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  • Action myoclonus--renal failure syndrome: characterization of a unique cerebro-renal disorder

    Year: 2004
    Journal: Brain
    Volume: 127
    Issue: 2004
    Page numbers: 2173-2182
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  • Action myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorder.
    Year: 2004
    Journal: Brain
    Volume: 127
    Page numbers: 2173-2182
    Publisher: Oxford University Press(Oxford)
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  • Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathy
    Year: 2004
    Journal: Annals of Neurology
    Volume: 55
    Page numbers: 550-557
    Publisher: Wiley-Liss(New York)
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  • Epilepsy in twins - Insights from unique historical data of William Lennox
    Year: 2004
    Journal: Neurology
    Volume: 62
    Page numbers: 1127-1133
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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  • Failure to confrim association of a polymorphism in ABCB1 with multidrug-resistant epilepsy
    Year: 2004
    Journal: Neurology
    Volume: 63
    Issue: 6
    Page numbers: 1090-1092
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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  • Familial partial epilepsy with variable foci: Clinical features and linkage to chromosome 22q12
    Year: 2004
    Journal: Epilepsia
    Volume: 45
    Issue: 9
    Page numbers: 1054-1060
    Publisher: Blackwell Science(Massachusetts)
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  • Febrile convulsions and genetic susceptibility: role of the neuronal nicotinic acetylcholine receptor α4 subunit
    Year: 2004
    Journal: Epilepsia
    Volume: 45
    Issue: 5
    Page numbers: 561
    Publisher: Blackwell Science(Massachusetts)
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  • GABRD encoding a protein for extra- or peri-synaptic GABA (A) receptors is a susceptibility locus for generalized epilepsies
    Year: 2004
    Journal: Human Molecular Genetics
    Volume: 13
    Issue: 13
    Page numbers: 1315-1319
    Publisher: Oxford University Press(Oxford)
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  • Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families
    Year: 2004
    Journal: Epilepsia
    Volume: 45
    Issue: 5
    Page numbers: 467-478
    Publisher: Blackwell Science(Massachusetts)
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  • Genetic association studies in epilepsy: "The truth is out there"
    Year: 2004
    Journal: Epilepsia
    Volume: 45
    Page numbers: 1429-1442
    Publisher: Blackwell Science(Massachusetts)
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  • Genetic variation of CACNA1H in idiopathic generalized epilepsy
    Year: 2004
    Journal: Annals of Neurology
    Volume: 55
    Issue: 4
    Page numbers: 595-596
    Publisher: Wiley-Liss(New York)
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  • Glioneuronal tumours in neurofibromatosis type 1: mRI-pathological study
    Year: 2004
    Journal: Journal of Clinical Neuroscience
    Volume: 11
    Issue: 7
    Page numbers: 745-747
    Publisher: Churchill Livingstone(Leith Walkedinburgh)
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  • Idiopathic recurrent stupor: a warning
    Year: 2004
    Journal: Journal of Neurology, Neurosurgery and Psychiatry
    Volume: 75
    Page numbers: 368-369
    Publisher: BMJ Publishing Group(London)
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  • Is benign rolandic epilepsy genetically determined?
    Year: 2004
    Journal: Annals of Neurology
    Volume: 56
    Page numbers: 129-132
    Publisher: Wiley-Liss(New York)
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  • Juvenile myoclonic epilepsy and idiopathic photosensitive occipital lobe epilepsy: is there overlap?
    Year: 2004
    Journal: Brain
    Volume: 127
    Page numbers: 1878-1886
    Publisher: Oxford University Press(Oxford)
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  • LGI1 mutations in temporal lobe epilepsies
    Year: 2004
    Journal: Neurology
    Volume: 62
    Page numbers: 1115-1119
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  • MR imaging and spectroscopic study of epileptogenic hypothalamic hamartomas: analysis of 72 cases
    Year: 2004
    Journal: American Journal of Neuroradiology
    Volume: 25
    Page numbers: 450-462
    Publisher: American Society of Neuroradiology
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  • Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction
    Year: 2004
    Journal: Journal of Medical Genetics
    Volume: 41
    Issue: 3
    Page numbers: e35
    Publisher: BMJ Publishing Group(London)
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  • Sandifer syndrome misdiagnosed as refractory partial seizures in an adult
    Year: 2004
    Journal: Epileptic Disorders
    Volume: 6
    Page numbers: 49-50
    Publisher: John Libbey Eurotext Ltd(Montrouge)
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  • Subtle microscopic abnormalities in hippocampal sclerosis do not predict clinical features of temporal lobe epilepsy
    Year: 2004
    Journal: Epilepsia
    Volume: 45
    Issue: 8
    Page numbers: 940-947
    Publisher: Blackwell Science(Massachusetts)
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  • Temporal lobe dysembryoplastic neuroepithelial tumour: significance of discordant interictal spikes
    Year: 2004
    Journal: Epileptic Disorders
    Volume: 6
    Issue: 2
    Page numbers: 107-114
    Publisher: John Libbey Eurotext Ltd(Montrouge)
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  • Temporal lobectomy: Long-term seizure outcome, late recurrence and risks for seizure recurrence
    Year: 2004
    Journal: Brain
    Volume: 127
    Issue: 9
    Page numbers: 2018-2030
    Publisher: Oxford University Press(Oxford)
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  • The idiopathic generalized epilepsies across life
    Year: 2004
    Journal: Clinical Neurophysiology Supplement
    Volume: 57
    Issue: 2004
    Page numbers: 408-414
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Publications in 2003

Journal Articles

  • Childhood absence epilepsy and febrile seizures: a family with a GABAA receptor


    Year: 2003
    Journal: Brain
    Volume: 126
    Page numbers: 230-240
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  • A twin study of genetic influences on Epilepsy outcome
    Year: 2003
    Journal: Twin Research
    Volume: 6
    Issue: 2
    Page numbers: 140-146
    Publisher: Australian Academic Press(Bowen Hills)
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  • Autosomal recessive form of periventricular heterotopia
    Year: 2003
    Journal: Neurology
    Volume: 60
    Page numbers: 1108-1112
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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  • Channelopathies as a genetic cause of epilepsy
    Year: 2003
    Journal: Current Opinion in Neurology
    Volume: 16
    Issue: 2
    Page numbers: 171-176
    Publisher: Lippincott Williams & Wilkins(Philadelphia)
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  • EEG in adult-onset idiopathic generalized epilepsy.
    Year: 2003
    Journal: Epilepsia
    Volume: 44
    Issue: 2
    Page numbers: 252-256
    Publisher: Blackwell Science(Massachusetts)
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  • Electroencephalographic characterisation of pentylenetetrazole-induced seizures in mice lacking the α4 subunit of the neuronal nicotinic receptor
    Year: 2003
    Journal: Neuropharmacology
    Volume: 44
    Page numbers: 234-243
    Publisher: Pergamon-Elsevier Science(Oxford)
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  • Epilepsy in offspring of whom both parents have idiopathic generalized epilepsy: Biparental inheritance.
    Year: 2003
    Journal: Epilepsia
    Volume: 44
    Issue: 9
    Page numbers: 1250-1254
    Publisher: Blackwell Science(Massachusetts)
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  • Generalized epilepsy in hypothalamic hamartoma - Evolution and postoperative resolution.
    Year: 2003
    Journal: Neurology
    Volume: 60
    Issue: 5
    Page numbers: 762-767
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  • Genetics of temporal lobe epilepsy
    Year: 2003
    Journal: Journal of Neurology, Neurosurgery and Psychiatry
    Volume: 74
    Page numbers: 1359-1361
    Publisher: BMJ Publishing Group(London)
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  • Hippocampal atrophy and T2-weighted signal changes in familial mesial temporal lobe epilepsy
    Year: 2003
    Journal: Neurology
    Volume: 60
    Page numbers: 405-409
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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  • Hypertensive encephalopathy: Antecedent to hippocampal sclerosis and temporal lobe epilepsy?
    Year: 2003
    Journal: Neurology
    Volume: 60
    Issue: 9
    Page numbers: 1534-1536
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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  • Hypertensive encephalopathy: Antecedent to hippocampal sclerosis