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Samuel Berkovic

Research Profile

Disorders

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Electroencephalography

Physiology

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Infants

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Publications

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Mark J Cook; Wendyl D'Souza; Gavin Fabinyi; John Archer; Samuel F Berkovic; Sean Hosking; Kent Leyde; Paul Lightfoot; Lucas Litewka; Andrew Morokoff; Michael Murphy; Terence J O'Brien; Vanessa Ruedebusch; W Douglas Sheffield; David Snyder; Raju Yerra; David Himes
Prediction of seizure likelihood with a long-term, implanted seizure advisory system in patients with drug-resistant epilepsy: a first-in-man study.
Shinichi Hirose; Marcelo Kauffman; Daniel H Lowenstein; Carla Marini; Ruth Ottman; Ingrid E Scheffer; Sanjay M Sisodiya; Nigel C K Tan; Eva Andermann; Samuel F Berkovic; Peter De Jonghe; Alica M Goldman
SCN1A testing for epilepsy: Application in clinical practice.
Sarah E Heron; Jacinta M McMahon; Yeh Sze Ong; Ingrid E Scheffer; Simone C Yendle; Samuel F Berkovic; Leanne M Dibbens
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies.

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All Publications

2013: Mark J Cook; Wendyl D'Souza; Gavin Fabinyi; John Archer; Samuel F Berkovic; Sean Hosking; Kent Leyde; Paul Lightfoot; Lucas Litewka; Andrew Morokoff; Michael Murphy; Terence J O'Brien; Vanessa Ruedebusch; W Douglas Sheffield; David Snyder; Raju Yerra; David Himes
Prediction of seizure likelihood with a long-term, implanted seizure advisory system in patients with drug-resistant epilepsy: a first-in-man study.
Lancet neurology 2013;12(6):563-71.
2013: Shinichi Hirose; Marcelo Kauffman; Daniel H Lowenstein; Carla Marini; Ruth Ottman; Ingrid E Scheffer; Sanjay M Sisodiya; Nigel C K Tan; Eva Andermann; Samuel F Berkovic; Peter De Jonghe; Alica M Goldman
SCN1A testing for epilepsy: Application in clinical practice.
Epilepsia 2013;54(5):946-52.
2013: Sarah E Heron; Jacinta M McMahon; Yeh Sze Ong; Ingrid E Scheffer; Simone C Yendle; Samuel F Berkovic; Leanne M Dibbens
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies.
Epilepsia 2013;54(5):e86-9.
2013: Michael S Hildebrand; Ingrid E Scheffer; Richard J H Smith; Hans-Henrik M Dahl; John Anthony Damiano; Samuel F Berkovic
Recent advances in the molecular genetics of epilepsy.
Journal of medical genetics 2013;50(5):271-9.
2013: Isabella Taylor; Samuel F Berkovic; Ingrid E Scheffer
Genetics of epilepsy syndromes in families with photosensitivity.
Neurology 2013;80(14):1322-9.
2013: Lysa Boissé Lomax; Mark A Corbett; Irenaeus F de Coo; Leanne M Dibbens; Luke C Gandolfo; Jozef Gecz; Helle Hjalgrim; Erik-Jan Kamsteeg; G Christoph Korenke; Anna-Elina Lehesjoki; Iris Marquardt; Rikke S Møller; John D O'Sullivan; Trine Prescott; Magnhild Rasmussen; Ines Said; Asbjørg Stray-Pedersen; Danya F Vears; Judith M A Verhagen; Annemarie M Vlaar; Michèl Willemsen; Kari M Aaberg; Melanie Bahlo; Marta A Bayly; Bastiaan R Bloem; Samuel F Berkovic
'North Sea' progressive myoclonus epilepsy: phenotype of subjects with GOSR2 mutation.
Brain : a journal of neurology 2013;136(Pt 4):1146-54.
2013: Katherine R Smith; John F Staropoli; Noreen A Alexander; Eva Andermann; Frederick Andermann; Samuel F Berkovic; Amalia C Bruni; Laura Canafoglia; Stirling Carpenter; Harold A Chapman; Jonathan D Cooper; Patrick Cossette; Hans-Henrik M Dahl; John Damiano; Silvana Franceschetti; Giorgio Giaccone; Joachim Grötzinger; Sara E Mole; Michela Morbin; Paul Saftig; Michael Schwake; Katherine B Sims; Melanie Bahlo
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis.
Human molecular genetics 2013;22(7):1417-23.
2013: Samuel F Berkovic; Jaideep Kapur
Are myotonia and epilepsy linked by a chloride channel?
Neurology 2013;80(12):1074-5.
2013: Christopher A Reid; A Marie Phillips; Samuel F Berkovic; Taehwan Kim; Jun Low; Bernhard Luscher; Steven Petrou
Multiple molecular mechanisms for a single GABAA mutation in epilepsy.
Neurology 2013;80(11):1003-8.
2013: Kurt Gleich; Marina Katerelos; Darren Lee; Paul Martinello; Peter F Mount; Marta A Bayly; Samuel F Berkovic; Michael J Desmond; Leanne M Dibbens; Scott A Fraser; Danya F Vears; David A Power
Abnormal Processing of Autophagosomes in Transformed B Lymphocytes from SCARB2-Deficient Subjects.
BioResearch open access 2013;2(1):40-6.
2013: Simone Mandelstam; George McGillivray; S Robertson; A Sandow; Samuel F Berkovic; Renzo Guerrini; Graeme D Jackson; Richard J Leventer; M van Kogelenberg; Ingrid E Scheffer
Bilateral posterior periventricular nodular heterotopia: a recognizable cortical malformation with a spectrum of associated brain abnormalities.
AJNR. American journal of neuroradiology 2013;34(2):432-8.
2013: Patrick W Carney; A Simon Harvey; Graeme D Jackson; Samuel F Berkovic; Ingrid E Scheffer
Siblings with refractory occipital epilepsy showing localized network activity on EEG-fMRI.
Epilepsia 2013;54(2):e28-32.
2013: Meng-Han Tsai; Samantha J Turner; Danya F Vears; Samuel F Berkovic; Lynette G Sadleir; Robert L Smith; Ingrid E Scheffer
Clinical genetic study of the epilepsy-aphasia spectrum.
Epilepsia 2013;54(2):280-7.
2013: Radwa A B Badawy; Samuel F Berkovic; Graeme D Jackson; Richard A L Macdonell
Cortical excitability and refractory epilepsy: a three-year longitudinal transcranial magnetic stimulation study.
International journal of neural systems 2013;23(1):1250030.
2013: Young Ok Kim; Carla Marini; Jacinta M McMahon; Davide Mei; Rima Nabbout; Samuel F Berkovic; Nicole Chemaly; Peter De Jonghe; Leanne M Dibbens; Renzo Guerrini; Xenia Iona; Arvid Suls; Ingrid E Scheffer
Do mutations in SCN1B cause Dravet syndrome?
Epilepsy research 2013;103(1):97-100.
2012: Todor Arsov; Samuel F Berkovic; Douglas E Crompton; Hans-Henrik M Dahl; John A Damiano; Linda L Huh; Kate M Lawrence; Saul A Mullen; Melinda Nolan; Lynette G Sadleir; Anaïs Thouin; Helen Young; Ingrid E Scheffer
Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.
Epilepsia 2012;53(12):e204-7.
2012: Ingrid E Scheffer; Zaid Afawi; Ian Andrews; Samuel F Berkovic; Hadassa Goldberg-Stern; Bronwyn E Grinton; Renzo Guerrini; Sarah E Heron; Xenia Iona; Maria Kinali; Sara Kivity; Carla Marini; Lynette G Sadleir; Leanne M Dibbens
PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures.
Neurology 2012;79(21):2104-8.
2012: Todor Arsov; Samuel F Berkovic; John A Damiano; Hadassa Goldberg-Stern; Sara Kivity; Kate M Lawrence; Saul A Mullen; Steven Petrou; A Marie Phillips; Sue Rogers; Zaid Afawi; Chantal Trager; Ingrid E Scheffer
Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.
Annals of neurology 2012;72(5):807-15.
2012: Sarah E Heron; Esther Kahana; Amos Korczyn; Laura Licchetta; Aziz Mazarib; Lino Nobili; Karen L Oliver; Steven Petrou; Giuseppe Plazzi; Ingrid E Scheffer; Katherine R Smith; Zaid Afawi; Melanie Bahlo; Samuel F Berkovic; Leanne M Dibbens
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy.
Nature genetics 2012;44(11):1188-90.
2012: Megan Oliva; Samuel F Berkovic; Steven Petrou
Sodium channels and the neurobiology of epilepsy.
Epilepsia 2012;53(11):1849-59.
2012: Susan E Tomlinson; Michael G Hanna; Samuel F Berkovic; Hugh Bostock; Bronwyn Grinton; Matthew C Kiernan; Dimitri M Kullmann; Ingrid E Scheffer; David Burke
In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remission.
Brain : a journal of neurology 2012;135(Pt 10):3144-52.
2012: Sarah L Velissaris; Samuel F Berkovic; Mark R Newton; Michael M Saling; Sarah J Wilson
Psychological trajectories in the year after a newly diagnosed seizure.
Epilepsia 2012;53(10):1774-81.
2012: Tiziana Pisano; Stephen Robertson; Felix Rosenow; Ingrid E Scheffer; Waney Squier; Pierre Thomas; Gaetano Tortorella; Eva Andermann; Frederick Andermann; A James Barkovich; Samuel F Berkovic; Susan Blaser; William B Dobyns; Richard J Leventer; Carla Marini; George McGillivray; Elena Parrini; Renzo Guerrini
Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis.
Neurology 2012;79(12):1244-51.
2012: Leanne M Dibbens; Katherine L Helbig; Bree L Hodgson; John C Mulley; Karen L Oliver; Samuel F Berkovic; Ingrid E Scheffer
Rare protein sequence variation in SV2A gene does not affect response to levetiracetam.
Epilepsy research 2012;101(3):277-9.
2012: Karl Martin Klein; Kate Lawrence; San San Xu; Alexandra Fischer; Samuel F Berkovic
Evidence for genetic factors in vasovagal syncope: a twin-family study.
Neurology 2012;79(6):561-5.
2012: Karl Martin Klein; John C Mulley; Terence J O'Brien; Kavita Praveen; Samuel F Berkovic; Simon Foote; Sarah E Heron; Ingrid E Scheffer
Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrum.
Epilepsia 2012;53(8):e151-5.
2012: Claudia Perandones; Marta A Bayly; Samuel F Berkovic; Federico E Micheli; Luis A Pellene; Leanne M Dibbens
A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2.
Movement disorders : official journal of the Movement Disorder Society 2012;27(9):1200-1.
2012: Lisa Bateman; Charles E Begley; Elinor Ben-Menachem; Anne T Berg; Samuel F Berkovic; Gregory D Cascino; Joseph Drazkowski; Jonathan C Edwards; Jerome Engel; Jacqueline A French; Frank D Gilliam; Matthew T Hoerth; Lara E Jehi; Andres M Kanner; Gregory Krauss; David M Labiner; Tobias Loddenkemper; Hans O Luders; Guy M McKhann; Richard McLachlan; Avani Modi; Page B Pennell; Patricia O Shafer; Joseph I Sirven; John M Stern; Jerzy P Szaflarski; William H Theodore
Overcoming barriers to successful epilepsy management.
Epilepsy currents / American Epilepsy Society 2012;12(4):158-60.
2012: Jill M Rodda; Ingrid E Scheffer; Samuel F Berkovic; Jacinta M McMahon; H Kerr Graham
Progressive gait deterioration in adolescents with Dravet syndrome.
Archives of neurology 2012;69(7):873-8.
2012: Katherine R Smith; John F Staropoli; Melanie Bahlo; Laura Canafoglia; Stirling Carpenter; Hans-Henrik Dahl; John Damiano; Dennis W Dickson; Silvana Franceschetti; Jada Lewis; Wen-Lang Lin; Sara E Mole; Michela Morbin; Davide Pareyson; Giacomina Rossi; Katherine B Sims; Samuel F Berkovic
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage.
American journal of human genetics 2012;90(6):1102-7.
2012: Anne M McIntosh; L Anne Mitchell; Clare A Averill; Gavin C A Fabinyi; Graeme D Jackson; Renate M Kalnins; Samuel F Berkovic
Long-term seizure outcome and risk factors for recurrence after extratemporal epilepsy surgery.
Epilepsia 2012;53(6):970-8.
2012: Daniel Carranza Rojo; John A Damiano; Leanne M Dibbens; Jeremy L Freeman; Deepak Gill; Xenia Iona; Richard J Leventer; Jacinta M McMahon; Todor Arsov; Samuel F Berkovic; A Simon Harvey; Angela Vincent; Ingrid E Scheffer
Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations.
Epilepsy research 2012;100(1-2):194-8.
2012: Douglas E Crompton; John W Dunne; Rosemary Harty; Kate M Lawrence; Lynette G Sadleir; Todor Arsov; Melanie Bahlo; Susannah T Bellows; Samuel F Berkovic; Catherine J Bromhead; Ingrid E Scheffer
Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus.
Archives of neurology 2012;69(4):474-81.
2012: Daniel W Kinsella; Clare A Averill; Samuel F Berkovic; Anne M McIntosh
Significance of post-operative auras after temporal lobectomy: a surprising methodological trap.
Epilepsy & behavior : E&B 2012;23(3):348-52.
2012: Danya F Vears; A Simon Harvey; Meng-Han Tsai; Samuel F Berkovic; Patrick W Carney; Bronwyn E Grinton; Leasha M Lillywhite; Lynette G Sadleir; Ingrid E Scheffer
Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes.
Epilepsia 2012;53(2):319-24.
2012: Radwa A B Badawy; Samuel F Berkovic; Graeme D Jackson; Richard A L Macdonell
Inter-session repeatability of cortical excitability measurements in patients with epilepsy.
Epilepsy research 2012;98(2-3):182-6.
2012: Sarah E Heron; Bree L Hodgson; James N Hughes; Xenia Iona; Sara Kivity; Amos D Korczyn; John C Mulley; James T Pelekanos; Clair Pridmore; Lynette G Sadleir; Ingrid E Scheffer; Paul Q Thomas; Sameer M Zuberi; Zaid Afawi; Haim Bassan; Samuel F Berkovic; Mark Corbett; Alison E Gardner; Jozef Gecz; Hadassa Goldberg-Stern; Bronwyn E Grinton; Eric Haan; Eric Herlenius; Leanne M Dibbens
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.
American journal of human genetics 2012;90(1):152-60.
2012: Sarah Weckhuysen; Simone Yendle; Iglika Yordanova; Dominique Audenaert; Samuel F Berkovic; Berten Ceulemans; Lieve R F Claes; Tine Deconinck; Liesbet Deprez; Danièle Hasaerts; Sarah E Heron; Dimitrina Hristova; An Jansen; Albena Jordanova; Lieven Lagae; Simone Mandelstam; John C Mulley; Filip Roelens; Ingrid E Scheffer; Katrien Smets; Thorsten Stanley; Arvid Suls; Peter de Jonghe
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
Annals of neurology 2012;71(1):15-25.
2011: John C Mulley; Ingrid E Scheffer; Danya F Vears; Bronwyn E Grinton; Marta A Bayly; Samuel F Berkovic; Tarishi Desai; Leanne M Dibbens
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes.
Epilepsia 2011;52(10):e139-42.
2011: Saul A Mullen; Ingrid E Scheffer; Arvid Suls; Kate Lawrence; Carla Marini; Davide Mei; Todor Arsov; Samuel F Berkovic; Daniela Buti; John Damiano; Peter De Jonghe; Elvio Della Giustina; Renzo Guerrini
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy.
Archives of neurology 2011;68(9):1152-5.
2011: Sarah von Spiczak; Samuel F Berkovic; Ursula Drechsel-Baeuerle; Ingo Helbig; Dick Lindhout; Hiltrud Muhle; Ingrid E Scheffer; Ulrich Stephani; Andreas van Baalen; Marjan J van Kempen; Brigitte Keller-Stanislawski
A retrospective population-based study on seizures related to childhood vaccination.
Epilepsia 2011;52(8):1506-12.
2011: Leanne M Dibbens; Ioannis Karakis; Marta A Bayly; Andrew J Cole; Daniel J Costello; Samuel F Berkovic
Mutation of SCARB2 in a patient with progressive myoclonus epilepsy and demyelinating peripheral neuropathy.
Archives of neurology 2011;68(6):812-3.
2011: M J Desmond; Scott A Fraser; K Gleich; Marina Katerelos; D Lee; Y Q Li; Paul Martinello; R Michelucci; Paul Saftig; M Schwake; D Stapleton; Merlin C Thomas; Samuel F Berkovic; A J Cole; David A Power
Tubular proteinuria in mice and humans lacking the intrinsic lysosomal protein SCARB2/Limp-2.
American journal of physiology. Renal physiology 2011;300(6):F1437-47.
2011: Todor Arsov; Katherine R Smith; John Damiano; Silvana Franceschetti; Laura Canafoglia; Catherine J Bromhead; Eva Andermann; Danya F Vears; Patrick Cossette; Sulekha Rajagopalan; Alan McDougall; Vito Sofia; Michael Farrell; Umberto Aguglia; Andrea Zini; Stefano Meletti; Michela Morbin; Saul Mullen; Frederick Andermann; Sara E Mole; Melanie Bahlo; Samuel F Berkovic
Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6.
American journal of human genetics 2011;88(5):566-73.
2011: Mark Corbett; Michael Schwake; Melanie Bahlo; Leanne M Dibbens; Meng Lin; Luke C Gandolfo; Danya F Vears; John D O'Sullivan; Thomas Robertson; Marta A Bayly; Alison E Gardner; Annemarie M Vlaar; G Christoph Korenke; Bastiaan R Bloem; Irenaeus F de Coo; Judith M A Verhagen; Anna-Elina Lehesjoki; Jozef Gecz; Samuel F Berkovic
A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia.
American journal of human genetics 2011;88(5):657-63.
2011: Angelo Labate; Antonio Gambardella; Eva Andermann; Umberto Aguglia; Fernando Cendes; Samuel F Berkovic; Frederick Andermann
Benign mesial temporal lobe epilepsy.
Nature reviews. Neurology 2011;7(4):237-40.
2011: Beverley M Essue; Stephen Jan; Maree L Hackett; Andrew F Bleasel; Carol A Ireland; Samuel F Berkovic; Craig S Anderson
Action to improve awareness, participation, care and support for people with epilepsy.
The Medical journal of Australia 2011;194(1):7-9.
2011: John C Mulley; Ingrid E Scheffer; Samuel F Berkovic; Sarah E Heron; Bree Hodgson; Xenia Iona; Leanne M Dibbens
The Role of Seizure-Related SEZ6 as a Susceptibility Gene in Febrile Seizures.
Neurology research international 2011;2011():917565.
2011: Christopher A Reid; Tae Hwan Kim; Samuel F Berkovic; Steven Petrou
Low blood glucose precipitates spike-and-wave activity in genetically predisposed animals.
Epilepsia 2011;52(1):115-20.
2011: Laura K Conlin; Whitney Kramer; Anne L Hutchinson; Xia Li; Harold Riethman; Hakon Hakonarson; John C Mulley; Ingrid E Scheffer; Samuel F Berkovic; Syed A Hosain; Nancy B Spinner
Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients.
Journal of medical genetics 2011;48(1):1-9.
2010: Zaid Afawi; Arvid Suls; Dana Ekstein; Sara Kivity; Miriam Y Neufeld; Karen Oliver; Peter De Jonghe; Amos D Korczyn; Samuel F Berkovic
Mild adolescent/adult onset epilepsy and paroxysmal exercise-induced dyskinesia due to GLUT1 deficiency.
Epilepsia 2010;51(12):2466-9.
2010: Hiltrud Muhle; Ines Steinich; Sarah von Spiczak; Andre Franke; Yvonne Weber; Holger Lerche; Michael Wittig; Simone Heidemann; Arvid Suls; Peter de Jonghe; Carla Marini; Renzo Guerrini; Ingrid E Scheffer; Samuel F Berkovic; Ulrich Stephani; Reiner Siebert; Thomas Sander; Ingo Helbig; Holger Tönnies
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy.
Epilepsia 2010;51(12):2453-6.
2010: Douglas E Crompton; Ingrid E Scheffer; Isabella Taylor; Mark J Cook; Penelope A McKelvie; Danya F Vears; Kate M Lawrence; Jacinta M McMahon; Bronwyn E Grinton; Anne M McIntosh; Samuel F Berkovic
Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance.
Brain : a journal of neurology 2010;133(11):3221-31.
2010: Christopher A Reid; Graeme D Jackson; Samuel F Berkovic; Steven Petrou
New therapeutic opportunities in epilepsy: a genetic perspective.
Pharmacology & therapeutics 2010;128(2):274-80.
2010: amal abou-hamden; Mandy Lau; Gavin Fabinyi; Samuel F Berkovic; Graeme D Jackson; L Anne Mitchell; Renate Kalnins; Greg Fitt; John S Archer
Small temporal pole encephaloceles: a treatable cause of "lesion negative" temporal lobe epilepsy.
Epilepsia 2010;51(10):2199-202.
2010: Radwa A B Badawy; Richard A L Macdonell; Graeme D Jackson; Samuel F Berkovic
Can changes in cortical excitability distinguish progressive from juvenile myoclonic epilepsy?
Epilepsia 2010;51(10):2084-8.
2010: Lata Vadlamudi; Leanne M Dibbens; Kate M Lawrence; Xenia Iona; Jacinta M McMahon; Wayne Murrell; Alan Mackay-Sim; Ingrid E Scheffer; Samuel F Berkovic
Timing of de novo mutagenesis--a twin study of sodium-channel mutations.
The New England journal of medicine 2010;363(14):1335-40.
2010: Liesbet Deprez; S Weckhuysen; P Holmgren; Arvid Suls; Tine Van Dyck; Dirk Goossens; Jurgen Del-Favero; A Jansen; K Verhaert; Lieven Lagae; Albena Jordanova; R Van Coster; S Yendle; Samuel F Berkovic; I Scheffer; Berten Ceulemans; Peter De Jonghe
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations.
Neurology 2010;75(13):1159-65.
2010: Mark Corbett; Melanie Bahlo; Lachlan Jolly; Zaid Afawi; Alison E Gardner; Karen L Oliver; Stanley Tan; Amy Coffey; John C Mulley; Leanne M Dibbens; Walid Simri; Adel Shalata; Sara Kivity; Graeme D Jackson; Samuel F Berkovic; Jozef Gecz
A focal epilepsy and intellectual disability syndrome is due to a mutation in TBC1D24.
American journal of human genetics 2010;87(3):371-5.
2010: Kate M Lawrence; Davide Mei; Mark R Newton; Richard J Leventer; Renzo Guerrini; Samuel F Berkovic
Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria.
Epilepsia 2010;51(9):1902-5.
2010: Jacinta M McMahon; Ingrid E Scheffer; Jillian K Nicholl; Wendy Waters; Helen Eyre; Lyn Hinton; Paul Nelson; Sui Yu; Leanne M Dibbens; Samuel F Berkovic; John C Mulley
Detection of microchromosomal aberrations in refractory epilepsy: a pilot study.
Epileptic disorders : international epilepsy journal with videotape 2010;12(3):192-8.
2010: Sarah E Heron; Ingrid E Scheffer; Bronwyn E Grinton; Helen Eyre; Karen L Oliver; Sharon Bain; Samuel F Berkovic; John C Mulley
Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3.
Epilepsia 2010;51(9):1865-9.
2010: Laura Mirandola; Radwa A Badawy; Ann M Saunders; Anne McIntosh; Samuel F Berkovic; Graeme D Jackson
Clinical features of seizures associated with parahippocampal/inferior temporal lesions compared to those with hippocampal sclerosis.
Epilepsia 2010;51(9):1906-9.
2010: Verena C Wimmer; Christopher A Reid; Suzanne Mitchell; Kay L Richards; Byron B Scaf; Bryan T Leaw; Elisa L Hill; Michel Royeck; Marie-Therese Horstmann; Brett A Cromer; Philip J Davies; Ruwei Xu; Holger Lerche; Samuel F Berkovic; Heinz Beck; Steven Petrou
Axon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus.
The Journal of clinical investigation 2010;120(8):2661-71.
2010: Raj D Sheth; Samuel F Berkovic
Key epilepsy gene gets further phenotypic delineation.
Neurology 2010;75(1):18-9.
2010: Sarah J Wilson; Joanne M Wrench; Anne M McIntosh; Peter F Bladin; Samuel F Berkovic
Profiles of psychosocial outcome after epilepsy surgery: the role of personality.
Epilepsia 2010;51(7):1133-8.
2010: Anne M McIntosh; Jacinta McMahon; Leanne M Dibbens; Xenia Iona; John C Mulley; Ingrid E Scheffer; Samuel F Berkovic
Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study.
Lancet neurology 2010;9(6):592-8.
2010: Verena C Wimmer; Christopher A Reid; Eva Y-W So; Samuel F Berkovic; Steven Petrou
Axon initial segment dysfunction in epilepsy.
The Journal of physiology 2010;588(Pt 11):1829-40.
2010: Richard J Leventer; Anna Jansen; Daniela T Pilz; Neil Stoodley; Carla Marini; Francois Dubeau; Jodie Malone; L Anne Mitchell; Simone Mandelstam; Ingrid E Scheffer; Samuel F Berkovic; Frederick Andermann; Eva Andermann; Renzo Guerrini; William B Dobyns
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients.
Brain : a journal of neurology 2010;133(Pt 5):1415-27.
2010: Leanne M Dibbens; Christopher A Reid; Bree L Hodgson; Evan A Thomas; Alison M Phillips; Elena Gazina; Brett A Cromer; Alison L Clarke; Tallie Z Baram; Ingrid E Scheffer; Samuel F Berkovic; Steven Petrou
Augmented currents of an HCN2 variant in patients with febrile seizure syndromes.
Annals of neurology 2010;67(4):542-6.
2010: Anne T Berg; Samuel F Berkovic; Martin J Brodie; Jeffrey Buchhalter; J Helen Cross; Walter van Emde Boas; Jerome Engel; Jacqueline French; Tracy A Glauser; Gary W Mathern; Solomon L Moshe; Douglas Nordli; Perrine Plouin; Ingrid E Scheffer
Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009.
Epilepsia 2010;51(4):676-85.
2010: Amanda G Wood; Michael M Saling; Marco Fedi; Samuel F Berkovic; Ingrid E Scheffer; Christopher Benjamin; David C Reutens
Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsy.
Epilepsy & behavior : E&B 2010;17(4):531-5.
2010: Nigel C K Tan; Samuel F Berkovic
The Epilepsy Genetic Association Database (epiGAD): analysis of 165 genetic association studies, 1996-2008.
Epilepsia 2010;51(4):686-9.
2010: Kim Hynes; Patrick Tarpey; Leanne M Dibbens; Marta A Bayly; Samuel F Berkovic; Raffaella Smith; Zahyia Al Raisi; Samantha J Turner; Natasha J Brown; Tarishi D Desai; Eric Haan; Gillian Turner; John Christodoulou; Helen Leonard; Deepak Gill; Michael R Stratton; Jozef Gecz; Ingrid E Scheffer
Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families.
Journal of medical genetics 2010;47(3):211-6.
2010: Samuel F Berkovic; Douglas E Crompton
The borderland of epilepsy: a clinical and molecular view, 100 years on.
Epilepsia 2010;51 Suppl 1():3-4.
2010: Sarah E Heron; Marta Hernandez; Caitlin Edwards; Edward Edkins; Floor E Jansen; Ingrid E Scheffer; Samuel F Berkovic; John C Mulley
Neonatal seizures and long QT syndrome: a cardiocerebral channelopathy?
Epilepsia 2010;51(2):293-6.
2010: Sandra J Petty; Keith Hill; Natalie E Haber; Lynda M Paton; Kate M Lawrence; Samuel F Berkovic; Markus J Seibel; Terence J O'Brien; John D Wark
Balance impairment in chronic antiepileptic drug users: a twin and sibling study.
Epilepsia 2010;51(2):280-8.
2010: Sarah E Heron; Ingrid E Scheffer; Xenia Iona; Sameer M Zuberi; Rachael Birch; Jacinta M McMahon; Carla M Bruce; Samuel F Berkovic; John C Mulley
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin.
Journal of medical genetics 2010;47(2):137-41.
2010: Gaby S Pell; Regula S Briellmann; Kate M Lawrence; Deborah Glencross; R Mark Wellard; Samuel F Berkovic; Graeme D Jackson
Reduced variance in monozygous twins for multiple MR parameters: implications for disease studies and the genetic basis of brain structure.
NeuroImage 2010;49(2):1536-44.
2010: Radwa A B Badawy; Richard A L Macdonell; Samuel F Berkovic; Mark R Newton; Graeme D Jackson
Predicting seizure control: cortical excitability and antiepileptic medication.
Annals of neurology 2010;67(1):64-73.
2010: Samuel F Berkovic
Epilepsy: insights into causes and treatment dilemmas.
Lancet neurology 2010;9(1):9-11.
2010: Ingrid E Scheffer; Samuel F Berkovic
Copy number variants--an unexpected risk factor for the idiopathic generalized epilepsies.
Brain : a journal of neurology 2010;133(Pt 1):7-8.
2009: Christopher P Derry; A Simon Harvey; Matthew C Walker; John S Duncan; Samuel F Berkovic
NREM arousal parasomnias and their distinction from nocturnal frontal lobe epilepsy: a video EEG analysis.
Sleep 2009;32(12):1637-44.
2009: Slave Petrovski; I E Scheffer; S M Sisodiya; Terence J O'Brien; Samuel F Berkovic
Lack of replication of association between scn1a SNP and febrile seizures.
Neurology 2009;73(22):1928-30.
2009: Neelan Pillay; Gavin C A Fabinyi; Terry S Myles; Gregory J Fitt; Samuel F Berkovic; Graeme D Jackson
Parahippocampal epilepsy with subtle dysplasia: A cause of "imaging negative" partial epilepsy.
Epilepsia 2009;50(12):2611-8.
2009: Leanne M Dibbens; R Michelucci; A Gambardella; Frederick Andermann; G Rubboli; M A Bayly; T Joensuu; D F Vears; S Franceschetti; L Canafoglia; R Wallace; A G Bassuk; D A Power; C A Tassinari; Eva Andermann; A E Lehesjoki; Samuel F Berkovic
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure.
Annals of neurology 2009;66(4):532-6.
2009: Evan A Thomas; Christopher A Reid; Samuel F Berkovic; Steven Petrou
Prediction by modeling that epilepsy may be caused by very small functional changes in ion channels.
Archives of neurology 2009;66(10):1225-32.
2009: Leanne M Dibbens; Saul Mullen; Ingo Helbig; Heather C Mefford; Marta A Bayly; Susannah Bellows; Costin Leu; Holger Trucks; Tanja Obermeier; Michael Wittig; Andre Franke; Hande Caglayan; Zuhal Yapici; Thomas Sander; Evan E Eichler; Ingrid E Scheffer; John C Mulley; Samuel F Berkovic
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance.
Human molecular genetics 2009;18(19):3626-31.
2009: Arvid Suls; Saul A Mullen; Yvonne G Weber; Kristien Verhaert; Berten Ceulemans; Renzo Guerrini; Thomas V Wuttke; Alberto Salvo-Vargas; Liesbet Deprez; Lieve R F Claes; Albena Jordanova; Samuel F Berkovic; Holger Lerche; Peter De Jonghe; Ingrid E Scheffer
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1.
Annals of neurology 2009;66(3):415-9.
2009: Radwa Badawy; Richard A L Macdonell; Graeme D Jackson; Samuel F Berkovic
Why do seizures in generalized epilepsy often occur in the morning?
Neurology 2009;73(3):218-22.
2009: Cassandra Szoeke; Graeme J Sills; Patrick Kwan; Slave Petrovski; Mark Newton; Nikolas Hitiris; Larry Baum; Samuel F Berkovic; Martin J Brodie; Leslie J Sheffield; Terence J O'Brien
Multidrug-resistant genotype (ABCB1) and seizure recurrence in newly treated epilepsy: data from international pharmacogenetic cohorts.
Epilepsia 2009;50(7):1689-96.
2009: Carla Marini; Ingrid E Scheffer; Rima Nabbout; Davide Mei; Kathy Cox; Leanne M Dibbens; Jacinta M McMahon; Xenia Iona; Rochio Sanchez Carpintero; Maurizio Elia; Maria Roberta Cilio; Nicola Specchio; Lucio Giordano; Pasquale Striano; Elena Gennaro; J Helen Cross; Sara Kivity; Miriam Y Neufeld; Zaid Afawi; Eva Andermann; Daniel Keene; Olivier Dulac; Federico Zara; Samuel F Berkovic; Renzo Guerrini; John C Mulley
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.
Epilepsia 2009;50(7):1670-8.
2009: Sarah L Velissaris; Sarah J Wilson; Mark R Newton; Samuel F Berkovic; Michael M Saling
Cognitive complaints after a first seizure in adulthood: Influence of psychological adjustment.
Epilepsia 2009;50(5):1012-21.
2009: Douglas E Crompton; Samuel F Berkovic
The borderland of epilepsy: clinical and molecular features of phenomena that mimic epileptic seizures.
Lancet neurology 2009;8(4):370-81.
2009: Angelique E J Sijben; Pasiri Sithinamsuwan; Ashalata Radhakrishnan; Radwa Badawy; Leanne M Dibbens; Aziz Mazarib; Dorit Lev; Tally Lerman-Sagie; Rachel Straussberg; Samuel F Berkovic; Ingrid E Scheffer
Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+?
Epilepsia 2009;50(4):953-6.
2009: S A Mullen; D E Crompton; P W Carney; Ingo Helbig; Samuel F Berkovic
A neurologist's guide to genome-wide association studies.
Neurology 2009;72(6):558-65.
2009: Christopher A Reid; Samuel F Berkovic; Steven Petrou
Mechanisms of human inherited epilepsies.
Progress in neurobiology 2009;87(1):41-57.
2009: Sarah J Wilson; Joanne M Wrench; Anne M McIntosh; Peter F Bladin; Samuel F Berkovic
Personality development in the context of intractable epilepsy.
Archives of neurology 2009;66(1):68-72.
2008: Ashalatha Radhakrishnan; Pasiri Sithinamsuwan; A Simon Harvey; Danny Flanagan; Gregory Fitt; Sam Berlangieri; Graeme D Jackson; Samuel F Berkovic; Ingrid E Scheffer
Multifocal epilepsy: the role of palliative resection - intractable frontal and occipital lobe epilepsy secondary to radiotherapy for acute lymphoblastic leukaemia.
Epileptic disorders : international epilepsy journal with videotape 2008;10(4):362-70.
2008: Ingo Helbig; Kate M Lawrence; Mary M Connellan; Yvonne Torn-Broers; Lata Vadlamudi; Jazmin Eckhaus; Roger L Milne; John L Hopper; Samuel F Berkovic
Obstetric events as a risk factor for febrile seizures: a community-based twin study.
Twin research and human genetics : the official journal of the International Society for Twin Studies 2008;11(6):634-40.
2008: Christopher P Derry; Sarah E Heron; Fiona Phillips; Stephen Howell; Jacinta MacMahon; Hilary A Phillips; John S Duncan; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer
Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability.
Epilepsia 2008;49(12):2125-9.
2008: Richard G H Cotton; Arleen D Auerbach; Myles Axton; Carol Isaacson Barash; Samuel F Berkovic; Anthony J Brookes; John Burn; Garry R Cutting; Johan T den Dunnen; Paul Flicek; Nelson Freimer; Marc S Greenblatt; Heather J Howard; Michael Katz; Finlay A Macrae; Donna Maglott; Gabriela Möslein; Sue Povey; Rajkumar S Ramesar; Carolyn S (Sue) Richards; Daniela Seminara; Timothy D Smith; María-Jesús Sobrido; Jan Helge Solbakk; Rudolph E Tanzi; Sean V Tavtigian; Graham Taylor; Joji Utsunomiya; Michael Watson
GENETICS. The Human Variome Project.
Science (New York, N.Y.) 2008;322(5903):861-2.
2008: Alexander G Bassuk; Robyn H Wallace; Aimee Buhr; Andrew R Buller; Zaid Afawi; Masahito Shimojo; Shingo Miyata; Shan Chen; Pedro Gonzalez-Alegre; Hilary L Griesbach; Shu Wu; Marcus Nashelsky; Eszter K Vladar; Dragana Antic; Polly J Ferguson; Sebahattin Cirak; Thomas Voit; Matthew P Scott; Jeffrey D Axelrod; Christina Gurnett; Azhar Daoud; Sara Kivity; Miriam Y Neufeld; Aziz Mazarib; Rachel Straussberg; Simri Walid; Amos D Korczyn; Diane C Slusarski; Samuel F Berkovic; Hatem El-Shanti
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.
American journal of human genetics 2008;83(5):572-81.
2008: Cindy Chiu; Christopher A Reid; Heneu O Tan; Philip J Davies; Frank N Single; Irene Koukoulas; Samuel F Berkovic; Seong-Seng Tan; Rolf Sprengel; Mathew V Jones; Steven Petrou
Developmental impact of a familial GABAA receptor epilepsy mutation.
Annals of neurology 2008;64(3):284-93.
2008: Isabella Taylor; Samuel F Berkovic; Sara Kivity; Ingrid E Scheffer
Benign occipital epilepsies of childhood: clinical features and genetics.
Brain : a journal of neurology 2008;131(Pt 9):2287-94.
2008: Ingo Helbig; Nicholas A Matigian; Lata Vadlamudi; Kate M Lawrence; Marta A Bayly; Sharon M Bain; Dileepa Diyagama; Ingrid E Scheffer; John C Mulley; Andrew J Holloway; Leanne M Dibbens; Samuel F Berkovic; Nicholas K Hayward
Gene expression analysis in absence epilepsy using a monozygotic twin design.
Epilepsia 2008;49(9):1546-54.
2008: Jean-Charles Hoda; Wenli Gu; Marc Friedli; Hilary A Phillips; Sonia Bertrand; Stylianos E Antonarakis; David Goudie; Richard Roberts; Ingrid E Scheffer; Carla Marini; Jayesh Patel; Samuel F Berkovic; John C Mulley; Ortrud K Steinlein; Daniel Bertrand
Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore.
Molecular pharmacology 2008;74(2):379-91.
2008: Arvid Suls; Peter Dedeken; Karolien Goffin; Hilde Van Esch; Patrick Dupont; David Cassiman; Judith Kempfle; Thomas V Wuttke; Yvonne Weber; Holger Lerche; Zaid Afawi; Wim Vandenberghe; Amos D Korczyn; Samuel F Berkovic; Dana Ekstein; Sara Kivity; Philippe Ryvlin; Lieve R F Claes; Liesbet Deprez; Snezana Maljevic; Alberto Vargas; Tine Van Dyck; Dirk Goossens; Jurgen Del-Favero; Koen Van Laere; Peter De Jonghe; Wim Van Paesschen
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.
Brain : a journal of neurology 2008;131(Pt 7):1831-44.
2008: Ingrid E Scheffer; Samantha J Turner; Leanne M Dibbens; Marta A Bayly; Kathryn Friend; Bree Hodgson; Linda Burrows; Marie Shaw; Chen Wei; Reinhard Ullmann; Hans-Hilger Ropers; Pierre Szepetowski; Eric Haan; Aziz Mazarib; Zaid Afawi; Miri Y Neufeld; P Ian Andrews; Geoffrey Wallace; Sara Kivity; Dorit Lev; Tally Lerman-Sagie; Christopher P Derry; Amos D Korczyn; Jozef Gecz; John C Mulley; Samuel F Berkovic
Epilepsy and mental retardation limited to females: an under-recognized disorder.
Brain : a journal of neurology 2008;131(Pt 4):918-27.
2008: Samuel F Berkovic; Leanne M Dibbens; Alicia Oshlack; Jeremy D Silver; Marina Katerelos; Danya F Vears; Renate Lüllmann-Rauch; Judith Blanz; Ke Wei Zhang; Jim Stankovich; Renate M Kalnins; John P Dowling; Eva Andermann; Frederick Andermann; Enrico Faldini; Rudi D'Hooge; Lata Vadlamudi; Richard A Macdonell; Bree L Hodgson; Marta A Bayly; Judy Savige; John C Mulley; Gordon K Smyth; David A Power; Paul Saftig; Melanie Bahlo
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis.
American journal of human genetics 2008;82(3):673-84.
2008: Ingo Helbig; Ingrid E Scheffer; John C Mulley; Samuel F Berkovic
Navigating the channels and beyond: unravelling the genetics of the epilepsies.
Lancet neurology 2008;7(3):231-45.
2008: Marco Fedi; Samuel F Berkovic; Richard A L Macdonell; Josie M Curatolo; Carla Marini; David C Reutens
Intracortical hyperexcitability in humans with a GABAA receptor mutation.
Cerebral cortex (New York, N.Y. : 1991) 2008;18(3):664-9.
2008: Robyn H Wallace; J L Freeman; M R Shouri; P A Izzillo; Jeffrey V Rosenfeld; John C Mulley; A Simon Harvey; Samuel F Berkovic
Somatic mutations in GLI3 can cause hypothalamic hamartoma and gelastic seizures.
Neurology 2008;70(8):653-5.
2008: Marco Fedi; Leon A Bach; Samuel F Berkovic; John O Willoughby; Ingrid E Scheffer; David C Reutens
Association of a nicotinic receptor mutation with reduced height and blunted physostigmine-stimulated growth hormone release.
The Journal of clinical endocrinology and metabolism 2008;93(2):634-7.
2007: Sarah E Heron; Houman Khosravani; Diego Varela; Christopher Bladen; Tristiana C Williams; Michelle R Newman; Ingrid E Scheffer; Samuel F Berkovic; John C Mulley; Gerald W Zamponi
Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.
Annals of neurology 2007;62(6):560-8.
2007: Sarah E Heron; K Cox; Bronwyn E Grinton; Sameer M Zuberi; S Kivity; Z Afawi; Rachel Straussberg; Samuel F Berkovic; Ingrid E Scheffer; John C Mulley
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.
Journal of medical genetics 2007;44(12):791-6.
2007: Ernest R Somerville; Daniel B McLaughlin; Martin K Robinson; Samuel F Berkovic
Adjunctive therapy of uncontrolled partial seizures with levetiracetam in Australian patients.
Epilepsy & behavior : E&B 2007;11(3):338-42.
2007: Leanne M Dibbens; Jenny Ekberg; I Taylor; Bree L Hodgson; S-J Conroy; Ingrid L Lensink; Sharad Kumar; M A Zielinski; Louise A Harkin; Grant R Sutherland; David J Adams; Samuel F Berkovic; Ingrid E Scheffer; John C Mulley; Philip Poronnik
NEDD4-2 as a potential candidate susceptibility gene for epileptic photosensitivity.
Genes, brain, and behavior 2007;6(8):750-5.
2007: Heneu O Tan; Christopher A Reid; Frank N Single; Philip J Davies; Cindy Chiu; Susan Murphy; Alison L Clarke; Leanne M Dibbens; Heinz E Krestel; John C Mulley; Mathew V Jones; Peter H Seeburg; Bert Sakmann; Samuel F Berkovic; Rolf Sprengel; Steven Petrou
Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(44):17536-41.
2007: Yaroslav Teper; Douglas Whyte; Elizabeth Cahir; Henry A Lester; Sharon R Grady; Michael J Marks; Bruce N Cohen; Carlos Fonck; Tristan McClure-Begley; J Michael McIntosh; Cesar Labarca; Andrew Lawrence; Feng Chen; Ilse Gantois; Philip J Davies; Steven Petrou; Mark Murphy; John Waddington; Malcolm K Horne; Samuel F Berkovic; John Drago
Nicotine-induced dystonic arousal complex in a mouse line harboring a human autosomal-dominant nocturnal frontal lobe epilepsy mutation.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2007;27(38):10128-42.
2007: Yu Hong Deng; Samuel F Berkovic; Ingrid E Scheffer
GEFS+ where focal seizures evolve from generalized spike wave: video-EEG study of two children.
Epileptic disorders : international epilepsy journal with videotape 2007;9(3):307-14.
2007: Isabella Taylor; Bree Hodgson; Ingrid E Scheffer; John C Mulley; Samuel F Berkovic; Leanne M Dibbens
Is photosensitive epilepsy less common in males due to variation in X chromosome photopigment genes?
Epilepsia 2007;48(9):1807-9.
2007: Ruwei Xu; Evan A Thomas; Elena V Gazina; K L Richards; M Quick; Robyn H Wallace; Louise A Harkin; Sarah E Heron; Samuel F Berkovic; Ingrid E Scheffer; John C Mulley; Steven Petrou
Generalized epilepsy with febrile seizures plus-associated sodium channel beta1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function.
Neuroscience 2007;148(1):164-74.
2007: Elodie Chabrol; Isabelle Gourfinkel-An; Ingrid E Scheffer; Fabienne Picard; Philippe Couarch; Samuel F Berkovic; Jacinta M McMahon; Nandita Bajaj; Luisa Mota-vieira; Rui Mota; Oriane Trouillard; Christel Depienne; Michel Baulac; Eric LeGuern; Stéphanie Baulac
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy.
Epilepsy research 2007;76(1):41-8.
2007: Ruwei Xu; Evan A Thomas; Misty Jenkins; Elena V Gazina; Cindy Chiu; Sarah E Heron; John C Mulley; Ingrid E Scheffer; Samuel F Berkovic; Steven Petrou
A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channel.
Molecular and cellular neurosciences 2007;35(2):292-301.
2007: Eric Herlenius; Sarah E Heron; Bronwyn E Grinton; Deborah Keay; Ingrid E Scheffer; John C Mulley; Samuel F Berkovic
SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum.
Epilepsia 2007;48(6):1138-42.
2007: Cristina Gomez-Abad; Zaid Afawi; Amos D Korczyn; Adel Misk; Stavit A Shalev; Ronen Spiegel; Tally Lerman-Sagie; Dorit Lev; Katherine L Kron; Pilar Gómez-Garre; José M Serratosa; Samuel F Berkovic
Founder effect with variable age at onset in Arab families with Lafora disease and EPM2A mutation.
Epilepsia 2007;48(5):1011-4.
2007: David L Weintrob; Michael M Saling; Samuel F Berkovic; David C Reutens
Impaired verbal associative learning after resection of left perirhinal cortex.
Brain : a journal of neurology 2007;130(Pt 5):1423-31.
2007: Sarah E Heron; Louisa Sanchez; Ingrid E Scheffer; Samuel F Berkovic; John C Mulley
Association studies and functional validation or functional validation alone?
Epilepsy research 2007;74(2-3):237-8.
2007: Gianpiero L Cavalleri; Nicole M Walley; Nicole Soranzo; John Mulley; Colin Doherty; Ashish Kapoor; Chantal Depondt; John M Lynch; Ingrid E Scheffer; Armin Heils; Anne Gehrmann; Peter Kinirons; Sonia Gandhi; Parthasarathy Satishchandra; Nicholas W Wood; Anuranjan Anand; Thomas Sander; Samuel F Berkovic; Norman Delanty; David B Goldstein; Sanjay M Sisodiya
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy.
Epilepsia 2007;48(4):706-12.
2007: Sarah E Heron; Ingrid E Scheffer; Samuel F Berkovic; Leanne M Dibbens; John C Mulley
Channelopathies in idiopathic epilepsy.
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 2007;4(2):295-304.
2007: Radwa Badawy; Josie M Curatolo; Mark Newton; Samuel F Berkovic; Richard A L Macdonell
Changes in cortical excitability differentiate generalized and focal epilepsy.
Annals of neurology 2007;61(4):324-31.
2007: Natasha J Brown; Samuel F Berkovic; Ingrid E Scheffer
Vaccination, seizures and 'vaccine damage'.
Current opinion in neurology 2007;20(2):181-7.
2007: Louise A Harkin; Jacinta M McMahon; Xenia Iona; Leanne M Dibbens; James T Pelekanos; Sameer M Zuberi; Lynette G Sadleir; Eva Andermann; Deepak Gill; Kevin Farrell; Mary Connolly; Thorsten Stanley; Michael Harbord; Frederick Andermann; Jing Wang; Sat Dev Batish; Jeffrey G Jones; William K Seltzer; Alison Gardner; Grant Sutherland; Samuel F Berkovic; John C Mulley; Ingrid E Scheffer
The spectrum of SCN1A-related infantile epileptic encephalopathies.
Brain : a journal of neurology 2007;130(Pt 3):843-52.
2007: Sarah L Velissaris; Sarah J Wilson; Michael M Saling; Mark R Newton; Samuel F Berkovic
The psychological impact of a newly diagnosed seizure: losing and restoring perceived control.
Epilepsy & behavior : E&B 2007;10(2):223-33.
2007: Regula S Briellmann; R Mark Wellard; Richard A J Masterton; David F Abbott; Samuel F Berkovic; Graeme D Jackson
Hippocampal sclerosis: MR prediction of seizure intractability.
Epilepsia 2007;48(2):315-23.
2007: Ingrid E Scheffer; Louise A Harkin; Bronwyn E Grinton; Leanne M Dibbens; Samantha J Turner; Marta A Zielinski; Ruwei Xu; Graeme Jackson; Judith Adams; Mary Connellan; Steven Petrou; R Mark Wellard; Regula S Briellmann; Robyn H Wallace; John C Mulley; Samuel F Berkovic
Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations.
Brain : a journal of neurology 2007;130(Pt 1):100-9.
2006: F E Jansen; Lynette G Sadleir; Louise A Harkin; Lata Vadlamudi; Jacinta M McMahon; John C Mulley; Ingrid E Scheffer; Samuel F Berkovic
Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults.
Neurology 2006;67(12):2224-6.
2006: C G Spooner; Samuel F Berkovic; L Anne Mitchell; Jacquie A Wrennall; A Simon Harvey
New-onset temporal lobe epilepsy in children: lesion on MRI predicts poor seizure outcome.
Neurology 2006;67(12):2147-53.
2006: Anne M McIntosh; Samuel F Berkovic
What happens now? Ongoing outcome after post-temporal lobectomy seizure recurrence.
Neurology 2006;67(9):1671-3.
2006: Christopher P Derry; John S Duncan; Samuel F Berkovic
Paroxysmal motor disorders of sleep: the clinical spectrum and differentiation from epilepsy.
Epilepsia 2006;47(11):1775-91.
2006: Lata Vadlamudi; D F Vears; A Hughes; E Pedagogus; Samuel F Berkovic
Action myoclonus-renal failure syndrome: a cause for worsening tremor in young adults.
Neurology 2006;67(7):1310-1.
2006: Bronwyn E Grinton; Ingrid E Scheffer; Samuel F Berkovic
Invited comments on the Shostak and Ottman review.
Epilepsia 2006;47(10):1751-2; author reply 1755-6.
2006: Anne Hempelmann; Kirsten P Taylor; Armin Heils; Susanne Lorenz; Jean-François Prud'homme; Rima Nabbout; Olivier Dulac; Gabrielle Rudolf; Federico Zara; Amedeo Bianchi; Robert Robinson; R Mark Gardiner; Athanasios Covanis; Dick Lindhout; Ulrich Stephani; Christian E Elger; Yvonne G Weber; Holger Lerche; Peter Nürnberg; Katherine L Kron; Ingrid E Scheffer; John C Mulley; Samuel F Berkovic; Thomas Sander
Exploration of the genetic architecture of idiopathic generalized epilepsies.
Epilepsia 2006;47(10):1682-90.
2006: John C Mulley; P Nelson; S Guerrero; Leanne M Dibbens; Xenia Iona; Jacinta M McMahon; Louise A Harkin; J Schouten; S Yu; Samuel F Berkovic; Ingrid E Scheffer
A new molecular mechanism for severe myoclonic epilepsy of infancy: exonic deletions in SCN1A.
Neurology 2006;67(6):1094-5.
2006: Radwa Badawy; Josie M Curatolo; M Newton; Samuel F Berkovic; Richard A L Macdonell
Sleep deprivation increases cortical excitability in epilepsy: syndrome-specific effects.
Neurology 2006;67(6):1018-22.
2006: Marco Fedi; Samuel F Berkovic; Carla Marini; Rachel Mulligan; Henri Tochon-Danguy; David C Reutens
A GABAA receptor mutation causing generalized epilepsy reduces benzodiazepine receptor binding.
NeuroImage 2006;32(3):995-1000.
2006: Nigel C K Tan; Samuel F Berkovic
Prediction of drug resistance in epilepsy: not as easy as ABC.
Lancet neurology 2006;5(8):641-2.
2006: Samuel F Berkovic; Steven Petrou
Febrile seizures: traffic slows in the heat.
Trends in molecular medicine 2006;12(8):343-4.
2006: Samuel F Berkovic; John C Mulley; Ingrid E Scheffer; Steven Petrou
Human epilepsies: interaction of genetic and acquired factors.
Trends in neurosciences 2006;29(7):391-7.
2006: Samuel F Berkovic; Louise A Harkin; Jacinta M McMahon; James T Pelekanos; Sameer M Zuberi; Elaine Wirrell; Deepak S Gill; Xenia Iona; John C Mulley; Ingrid E Scheffer
De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study.
Lancet neurology 2006;5(6):488-92.
2006: Christopher Paul Derry; Margot Davey; Murray Johns; Katie Kron; Deborah Glencross; Carla Marini; Ingrid E Scheffer; Samuel F Berkovic
Distinguishing sleep disorders from seizures: diagnosing bumps in the night.
Archives of neurology 2006;63(5):705-9.
2006: Patrice Roll; Gabrielle Rudolf; Sandrine Pereira; Barbara Royer-Zemmour; Ingrid E Scheffer; Annick Massacrier; Maria-Paola Valenti; Nathalie Roeckel-Trevisiol; Sarah Jamali; Christophe Beclin; Caroline Seegmuller; Marie-Noëlle Metz-Lutz; Arnaud Lemainque; Marc Delepine; Christophe Caloustian; Anne De Saint-Martin; Nadine Bruneau; Danièle Depétris; Marie-Geneviève Mattéi; Elisabeth Flori; Andrée Robaglia-Schlupp; Nicolas Lévy; Bernd A Neubauer; Rivka Ravid; Christian Marescaux; Samuel F Berkovic; Edouard Hirsch; Mark Lathrop; Pierre Cau; Pierre Szepetowski
SRPX2 mutations in disorders of language cortex and cognition.
Human molecular genetics 2006;15(7):1195-207.
2006: Christopher Derry; Christopher Benjamin; Peter Bladin; Didier le Bars; Henri Tochon-Danguy; Samuel F Berkovic; Luc Zimmer; Nicolas Costes; Rachel Mulligan; David C Reutens
Increased serotonin receptor availability in human sleep: evidence from an [18F]MPPF PET study in narcolepsy.
NeuroImage 2006;30(2):341-8.
2006: Lata Vadlamudi; Marianne Juel Kjeldsen; Linda A Corey; Marit H Solaas; Mogens Laue Friis; John M Pellock; Karl O Nakken; Roger L Milne; Ingrid E Scheffer; A Simon Harvey; John L Hopper; Samuel F Berkovic
Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaboration.
Epilepsia 2006;47(3):550-5.
2006: Cassandra E I Szoeke; Mark Newton; Julie M Wood; David Goldstein; Samuel F Berkovic; Terrence J OBrien; Les J Sheffield
Update on pharmacogenetics in epilepsy: a brief review.
Lancet neurology 2006;5(2):189-96.
2005: Samuel F Berkovic
Treatment with anti-epileptic drugs.
Australian family physician 2005;34(12):1017-20.
2005: S J Petty; Lynda M Paton; Terence J O'Brien; Joanna Makovey; B Erbas; Philip Sambrook; Samuel F Berkovic; John D Wark
Effect of antiepileptic medication on bone mineral measures.
Neurology 2005;65(9):1358-65.
2005: Glenn P Ollenberger; Amanda J Byrne; Salvatore U Berlangieri; Christopher C Rowe; Kunthi Pathmaraj; David C Reutens; Samuel F Berkovic; Ingrid E Scheffer; Andrew M Scott
Assessment of the role of FDG PET in the diagnosis and management of children with refractory epilepsy.
European journal of nuclear medicine and molecular imaging 2005;32(11):1311-6.
2005: John C Mulley; Ingrid E Scheffer; Louise A Harkin; Samuel F Berkovic; Leanne M Dibbens
Susceptibility genes for complex epilepsy.
Human molecular genetics 2005;14 Spec No. 2():R243-9.
2005: Melodie R Winawer; Carla Marini; Bronwyn E Grinton; daniel rabinowitz; Samuel F Berkovic; Ingrid E Scheffer; Ruth Ottman
Familial clustering of seizure types within the idiopathic generalized epilepsies.
Neurology 2005;65(4):523-8.
2005: Matthew C Kiernan; Arun V Krishnan; Cindy S-Y Lin; David Burke; Samuel F Berkovic
Mutation in the Na+ channel subunit SCN1B produces paradoxical changes in peripheral nerve excitability.
Brain : a journal of neurology 2005;128(Pt 8):1841-6.
2005: Anne M McIntosh; Samuel F Berkovic
Treatment of new-onset epilepsy: seizures beget discussion.
Lancet 2005;365(9476):1985-6.
2005: John C Mulley; Ingrid E Scheffer; Steven Petrou; Leanne M Dibbens; Samuel F Berkovic; Louise A Harkin
SCN1A mutations and epilepsy.
Human mutation 2005;25(6):535-42.
2005: Nigel C K Tan; Sarah E Heron; Ingrid E Scheffer; Samuel F Berkovic; John C Mulley
Is variation in the GABA(B) receptor 1 gene associated with temporal lobe epilepsy?
Epilepsia 2005;46(5):778-80.
2005: Samuel F Berkovic; Aziz Mazarib; Simri Walid; Miri Y Neufeld; Judith Manelis; Yoram Nevo; Amos D Korczyn; Jinggang Yin; Lan Xiong; Massimo Pandolfo; John C Mulley; Robyn H Wallace
A new clinical and molecular form of Unverricht-Lundborg disease localized by homozygosity mapping.
Brain : a journal of neurology 2005;128(Pt 3):652-8.
2005: Anne M McIntosh; Renate M Kalnins; L Anne Mitchell; Samuel F Berkovic
Early seizures after temporal lobectomy predict subsequent seizure recurrence.
Annals of neurology 2005;57(2):283-8.
2005: Rachel Straussberg; Lina Basel-Vanagaite; Sara Kivity; Ron Dabby; S Cirak; P Nurnberg; Thomas Voit; Muhammad Mahajnah; Dov Inbar; G M Saifi; J R Lupski; Valérie Delague; André Megarbane; A Richter; E Leshinsky; Samuel F Berkovic
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures.
Neurology 2005;64(1):142-4.
2005: Angelo Labate; Mark R Newton; Graeme M Vernon; Samuel F Berkovic
Tramadol and new-onset seizures.
The Medical journal of Australia 2005;182(1):42-3.
2005: Ingrid E Scheffer; Louise A Harkin; Leanne M Dibbens; John C Mulley; Samuel F Berkovic
Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+).
Epilepsia 2005;46 Suppl 10():41-7.
2005: Roy G Beran; Samuel F Berkovic; Andrew B Black; Gytis Danta; Reinhard Hiersemenzel; Graham J Schapel; Frank J E Vajda
Efficacy and safety of levetiracetam 1000-3000 mg/day in patients with refractory partial-onset seizures: a multicenter, open-label single-arm study.
Epilepsy research 2005;63(1):1-9.
2004: Ron Granot; Samuel F Berkovic; Scott Patterson; Malcolm Hopwood; Olaf H Drummer; Rod Mackenzie
Endozepine stupor: disease or deception? A critical review.
Sleep 2004;27(8):1597-9.
2004: Nigel C K Tan; John C Mulley; Samuel F Berkovic
Genetic association studies in epilepsy: "the truth is out there".
Epilepsia 2004;45(11):1429-42.
2004: AmanPreet Badhwar; Samuel F Berkovic; John P Dowling; Michael Gonzales; Sridar Narayanan; Amy Brodtmann; Leon Berzen; John Caviness; Claudia Trenkwalder; Juliane Winkelmann; Jean Rivest; Marie Lambert; Otto Hernandez-Cossio; Stirling Carpenter; Frederick Andermann; Eva Andermann
Action myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorder.
Brain : a journal of neurology 2004;127(Pt 10):2173-82.
2004: Nigel C K Tan; Sarah E Heron; Ingrid E Scheffer; James T Pelekanos; Jacinta M McMahon; D F Vears; John C Mulley; Samuel F Berkovic
Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsy.
Neurology 2004;63(6):1090-2.
2004: Marco Fedi; L Anne Mitchell; Renate M Kalnins; David H Gutmann; Arie Perry; Mark Newton; Amy Brodtmann; Samuel F Berkovic
Glioneuronal tumours in neurofibromatosis type 1: MRI-pathological study.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2004;11(7):745-7.
2004: Samuel F Berkovic; José M Serratosa; Hilary A Phillips; Lan Xiong; Eva Andermann; Fernando Díaz-Otero; Pilar Gómez-Garre; Mercedes Martín; Yolanda Fernández-Bullido; Frederick Andermann; Iscia Lopes-Cendes; Francois Dubeau; Richard Desbiens; Ingrid E Scheffer; Robyn H Wallace; John C Mulley; Massimo Pandolfo
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.
Epilepsia 2004;45(9):1054-60.
2004: Anne M McIntosh; Renate M Kalnins; L Anne Mitchell; Gavin C A Fabinyi; Regula S Briellmann; Samuel F Berkovic
Temporal lobectomy: long-term seizure outcome, late recurrence and risks for seizure recurrence.
Brain : a journal of neurology 2004;127(Pt 9):2018-30.
2004: Renate M Kalnins; Anne McIntosh; Michael M Saling; Samuel F Berkovic; Graeme D Jackson; Regula S Briellmann
Subtle microscopic abnormalities in hippocampal sclerosis do not predict clinical features of temporal lobe epilepsy.
Epilepsia 2004;45(8):940-7.
2004: Isabella Taylor; Carla Marini; Michael R Johnson; Samantha Turner; Samuel F Berkovic; Ingrid E Scheffer
Juvenile myoclonic epilepsy and idiopathic photosensitive occipital lobe epilepsy: is there overlap?
Brain : a journal of neurology 2004;127(Pt 8):1878-86.
2004: Lata Vadlamudi; A Simon Harvey; Mary M Connellan; Roger L Milne; John L Hopper; Ingrid E Scheffer; Samuel F Berkovic
Is benign rolandic epilepsy genetically determined?
Annals of neurology 2004;56(1):129-32.
2004: Leanne M Dibbens; Hua-Jun Feng; Michaella C Richards; Louise A Harkin; Bree L Hodgson; Darren Scott; Misty Jenkins; Steven Petrou; Grant R Sutherland; Ingrid E Scheffer; Samuel F Berkovic; Robert L Macdonald; John C Mulley
GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies.
Human molecular genetics 2004;13(13):1315-9.
2004: Angelo Labate; Regula S Briellmann; A Simon Harvey; Samuel F Berkovic; Paolo Federico; Renate M Kalnins; Gavin C A Fabinyi; Graeme D Jackson
Temporal lobe dysembryoplastic neuroepithelial tumour: significance of discordant interictal spikes.
Epileptic disorders : international epilepsy journal with videotape 2004;6(2):107-14.
2004: Carla Marini; Ingrid E Scheffer; Kathryn M Crossland; Bronwyn E Grinton; Fiona L Phillips; Jacinta M McMahon; Samantha J Turner; Joanne T Dean; Sara Kivity; Aziz Mazarib; Miri Y Neufeld; Amos D Korczyn; Louise A Harkin; Leanne M Dibbens; Robyn H Wallace; John C Mulley; Samuel F Berkovic
Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.
Epilepsia 2004;45(5):467-78.
2004: Lata Vadlamudi; Eva Andermann; C T Lombroso; S C Schachter; Roger L Milne; John L Hopper; Frederick Andermann; Samuel F Berkovic
Epilepsy in twins: insights from unique historical data of William Lennox.
Neurology 2004;62(7):1127-33.
2004: Samuel F Berkovic; P Izzillo; Jacinta M McMahon; Louise A Harkin; Anne M McIntosh; Hilary A Phillips; Regula S Briellmann; Robyn H Wallace; Aziz Mazarib; Miri Y Neufeld; Amos D Korczyn; Ingrid E Scheffer; John C Mulley
LGI1 mutations in temporal lobe epilepsies.
Neurology 2004;62(7):1115-9.
2004: Sarah E Heron; Hilary A Phillips; John C Mulley; Aziz Mazarib; Miri Y Neufeld; Samuel F Berkovic; Ingrid E Scheffer
Genetic variation of CACNA1H in idiopathic generalized epilepsy.
Annals of neurology 2004;55(4):595-6.
2004: Samuel F Berkovic; Sarah E Heron; Lucio Giordano; Carla Marini; Renzo Guerrini; Robert E Kaplan; Antonio Gambardella; Ortrud K Steinlein; Bronwyn E Grinton; Joanne T Dean; Laura Bordo; Bree L Hodgson; Toshiyuki Yamamoto; John C Mulley; Federico Zara; Ingrid E Scheffer
Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy.
Annals of neurology 2004;55(4):550-7.
2004: Sriudomkajorn Somjit; Yong Lee; Samuel F Berkovic; A Simon Harvey
Sandifer syndrome misdiagnosed as refractory partial seizures in an adult.
Epileptic disorders : international epilepsy journal with videotape 2004;6(1):49-50.
2004: Jeremy L Freeman; Lee Coleman; R Mark Wellard; Michael J Kean; Jeffrey V Rosenfeld; Graeme D Jackson; Samuel F Berkovic; A Simon Harvey
MR imaging and spectroscopic study of epileptogenic hypothalamic hamartomas: analysis of 72 cases.
AJNR. American journal of neuroradiology 2004;25(3):450-62.
2004: Michaella C Richards; Sarah E Heron; Hayley E Spendlove; Ingrid E Scheffer; Bronwyn E Grinton; Samuel F Berkovic; John C Mulley; A Davy
Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction.
Journal of medical genetics 2004;41(3):e35.
2004: Ron Granot; Samuel F Berkovic; S Patterson; M Hopwood; R Mackenzie
Idiopathic recurrent stupor: a warning.
Journal of neurology, neurosurgery, and psychiatry 2004;75(3):368-9.
2003: A Simon Harvey; Jeremy L Freeman; Samuel F Berkovic; Jeffrey V Rosenfeld
Transcallosal resection of hypothalamic hamartomas in patients with intractable epilepsy.
Epileptic disorders : international epilepsy journal with videotape 2003;5(4):257-65.
2003: Frederick Andermann; Alexis Arzimanoglou; Samuel F Berkovic
Hypothalamic hamartoma and epilepsy: the pathway of discovery.
Epileptic disorders : international epilepsy journal with videotape 2003;5(4):173-5.
2003: Lata Vadlamudi; I E Scheffer; Samuel F Berkovic
Genetics of temporal lobe epilepsy.
Journal of neurology, neurosurgery, and psychiatry 2003;74(10):1359-61.
2003: Kenneth Opeskin; Samuel F Berkovic
Risk factors for sudden unexpected death in epilepsy: a controlled prospective study based on coroners cases.
Seizure : the journal of the British Epilepsy Association 2003;12(7):456-64.
2003: Robyn H Wallace; Bree L Hodgson; Bronwyn E Grinton; R M Gardiner; R Robinson; V Rodriguez-Casero; Lynette G Sadleir; J Morgan; Louise A Harkin; Leanne M Dibbens; T Yamamoto; Eva Andermann; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer
Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms.
Neurology 2003;61(6):765-9.
2003: Andrew B Black; Samuel F Berkovic
New driving guidelines: ethical and legal uncertainties.
The Medical journal of Australia 2003;179(6):327-8.
2003: Carla Marini; A Simon Harvey; James T Pelekanos; Samuel F Berkovic
Epilepsy in offspring of whom both parents have idiopathic generalized epilepsy: biparental inheritance.
Epilepsia 2003;44(9):1250-4.
2003: Ingrid E Scheffer; Samuel F Berkovic
The genetics of human epilepsy.
Trends in pharmacological sciences 2003;24(8):428-33.
2003: Samuel F Berkovic; Alexis Arzimanoglou; Ruben Kuzniecky; A Simon Harvey; André Palmini; Frederick Andermann
Hypothalamic hamartoma and seizures: a treatable epileptic encephalopathy.
Epilepsia 2003;44(7):969-73.
2003: Carlo Solinas; Regula S Briellmann; A Simon Harvey; L Anne Mitchell; Samuel F Berkovic
Hypertensive encephalopathy: antecedent to hippocampal sclerosis and temporal lobe epilepsy?
Neurology 2003;60(9):1534-6.
2003: Michael R Johnson; Roger L Milne; Yvonne Torn-Broers; John L Hopper; Ingrid E Scheffer; Samuel F Berkovic
A twin study of genetic influences on epilepsy outcome.
Twin research : the official journal of the International Society for Twin Studies 2003;6(2):140-6.
2003: Ailsa McLellan; Hilary A Phillips; Christopher Rittey; Martin Kirkpatrick; John C Mulley; David R Goudie; John B P Stephenson; John Tolmie; Ingrid E Scheffer; Samuel F Berkovic; Sameer M Zuberi
Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsy.
Epilepsia 2003;44(4):613-7.
2003: John C Mulley; Ingrid E Scheffer; Steven Petrou; Samuel F Berkovic
Channelopathies as a genetic cause of epilepsy.
Current opinion in neurology 2003;16(2):171-6.
2003: Isabella Taylor; Ingrid E Scheffer; Samuel F Berkovic
Occipital epilepsies: identification of specific and newly recognized syndromes.
Brain : a journal of neurology 2003;126(Pt 4):753-69.
2003: Jeremy L Freeman; A Simon Harvey; Jeffrey V Rosenfeld; Jacquie A Wrennall; C A Bailey; Samuel F Berkovic
Generalized epilepsy in hypothalamic hamartoma: evolution and postoperative resolution.
Neurology 2003;60(5):762-7.
2003: Craig McColl; Malcolm K Horne; David Finkelstein; John Y F Wong; Samuel F Berkovic; John Drago
Electroencephalographic characterisation of pentylenetetrazole-induced seizures in mice lacking the alpha 4 subunit of the neuronal nicotinic receptor.
Neuropharmacology 2003;44(2):234-43.
2003: Suthida Yenjun; A Simon Harvey; Carla Marini; Mark R Newton; Mark A King; Samuel F Berkovic
EEG in adult-onset idiopathic generalized epilepsy.
Epilepsia 2003;44(2):252-6.
2003: Carla Marini; Mark A King; John S Archer; Mark R Newton; Samuel F Berkovic
Idiopathic generalised epilepsy of adult onset: clinical syndromes and genetics.
Journal of neurology, neurosurgery, and psychiatry 2003;74(2):192-6.
2003: Carla Marini; Louise A Harkin; Robyn H Wallace; John C Mulley; Ingrid E Scheffer; Samuel F Berkovic
Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation.
Brain : a journal of neurology 2003;126(Pt 1):230-40.
2002: David N Bowser; David A Wagner; Cynthia Czajkowski; Brett A Cromer; Michael W Parker; Robyn H Wallace; Louise A Harkin; John C Mulley; Carla Marini; Samuel F Berkovic; David A Williams; Mathew V Jones; Steven Petrou
Altered kinetics and benzodiazepine sensitivity of a GABAA receptor subunit mutation [gamma 2(R43Q)] found in human epilepsy.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(23):15170-5.
2002: Jonathan W Sturm; Marco Fedi; Samuel F Berkovic; David C Reutens
Exercise-induced temporal lobe epilepsy.
Neurology 2002;59(8):1246-8.
2002: Sarah E Heron; Kathryn M Crossland; Eva Andermann; Hilary A Phillips; Allison J Hall; Andrew F Bleasel; Michael Shevell; Suha Mercho; Marie-Hélène Seni; Marie-Christine Guiot; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer
Sodium-channel defects in benign familial neonatal-infantile seizures.
Lancet 2002;360(9336):851-2.
2002: Ingrid E Scheffer; Robyn H Wallace; Fiona L Phillips; P Hewson; K Reardon; G Parasivam; P Stromme; Samuel F Berkovic; Jozef Gecz; John C Mulley
X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARX.
Neurology 2002;59(3):348-56.
2002: Richard A L Macdonell; Josie M Curatolo; Samuel F Berkovic
Transcranial magnetic stimulation and epilepsy.
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society 2002;19(4):294-306.
2002: John Y F Wong; Shelley A Ross; Craig McColl; Jim S Massalas; Emma Powney; David Finkelstein; Malcolm Clark; Malcolm K Horne; Samuel F Berkovic; John Drago
Proconvulsant-induced seizures in alpha(4) nicotinic acetylcholine receptor subunit knockout mice.
Neuropharmacology 2002;43(1):55-64.
2002: Robyn H Wallace; Ingrid E Scheffer; G Parasivam; S Barnett; G B Wallace; Grant R Sutherland; Samuel F Berkovic; John C Mulley
Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B.
Neurology 2002;58(9):1426-9.
2002: Regula S Briellmann; Samuel F Berkovic; Ari Syngeniotis; Mark A King; Graeme D Jackson
Seizure-associated hippocampal volume loss: a longitudinal magnetic resonance study of temporal lobe epilepsy.
Annals of neurology 2002;51(5):641-4.
2002: David L Weintrob; Michael M Saling; Samuel F Berkovic; Salvatore U Berlangieri; David C Reutens
Verbal memory in left temporal lobe epilepsy: evidence for task-related localization.
Annals of neurology 2002;51(4):442-7.
2002: Rita Singh; R J McKinlay Gardner; Kathryn M Crossland; Ingrid E Scheffer; Samuel F Berkovic
Chromosomal abnormalities and epilepsy: a review for clinicians and gene hunters.
Epilepsia 2002;43(2):127-40.
2002: Louise A Harkin; David N Bowser; Leanne M Dibbens; Rita Singh; Fiona L Phillips; Robyn H Wallace; Michaella C Richards; David A Williams; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer; Steven Petrou
Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plus.
American journal of human genetics 2002;70(2):530-6.
2002: Regula S Briellmann; Renate M Kalnins; Samuel F Berkovic; Graeme D Jackson
Hippocampal pathology in refractory temporal lobe epilepsy: T2-weighted signal change reflects dentate gliosis.
Neurology 2002;58(2):265-71.
2002: Gregory R Savage; Michael M Saling; Christopher W Davis; Samuel F Berkovic
Direct and indirect measures of verbal relational memory following anterior temporal lobectomy.
Neuropsychologia 2002;40(3):302-16.
2001: Paul McCrory; Samuel F Berkovic
Concussion: the history of clinical and pathophysiological concepts and misconceptions.
Neurology 2001;57(12):2283-9.
2001: Regula S Briellmann; Yvonne Torn-Broers; Graeme D Jackson; Samuel F Berkovic
Seizures in family members of patients with hippocampal sclerosis.
Neurology 2001;57(10):1800-4.
2001: Regula S Briellmann; Yvonne Torn-Broers; Samuel F Berkovic
Idiopathic generalized epilepsies: do sporadic and familial cases differ?
Epilepsia 2001;42(11):1399-402.
2001: Ingrid E Scheffer; R Wallace; J C Mulley; Samuel F Berkovic
Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome).
Brain & development 2001;23(7):732-5.
2001: Roy G Beran; Samuel F Berkovic; A Black; G Danta; J Dunne; J Frasca; K Grainger; C Kilpatrick; R McKenzie; D McLaughlin; G Schapel; E Somerville
AUStralian study of titration to effect profile of safety (AUS-STEPS): high-dose gabapentin (neurontin) in partial seizures.
Epilepsia 2001;42(10):1335-9.
2001: A M McIntosh; S J Wilson; Samuel F Berkovic
Seizure outcome after temporal lobectomy: current research practice and findings.
Epilepsia 2001;42(10):1288-307.
2001: Aziz Mazarib; Lan Xiong; Miri Y Neufeld; Miriam Birnbaum; Amos D Korczyn; Massimo Pandolfo; Samuel F Berkovic
Unverricht-Lundborg disease in a five-generation Arab family: instability of dodecamer repeats.
Neurology 2001;57(6):1050-4.
2001: Richard A L Macdonell; M A King; M R Newton; Josie M Curatolo; D C Reutens; Samuel F Berkovic
Prolonged cortical silent period after transcranial magnetic stimulation in generalized epilepsy.
Neurology 2001;57(4):706-8.
2001: Rita Singh; Eva Andermann; W P Whitehouse; A Simon Harvey; D L Keene; Marie-Hélène Seni; Kathryn M Crossland; Frederick Andermann; Samuel F Berkovic; Ingrid E Scheffer
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?
Epilepsia 2001;42(7):837-44.
2001: Robyn H Wallace; Carla Marini; Steven Petrou; Louise A Harkin; David N Bowser; Rekha G Panchal; David A Williams; Grant R Sutherland; John C Mulley; Ingrid E Scheffer; Samuel F Berkovic
Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures.
Nature genetics 2001;28(1):49-52.
2001: Robyn H Wallace; Ingrid E Scheffer; S Barnett; M Richards; Leanne M Dibbens; R R Desai; Tally Lerman-Sagie; D Lev; Aziz Mazarib; N Brand; Bruria Ben-Zeev; Igor Goikhman; Rita Singh; Gabriel Kremmidiotis; Alison Gardner; Grant R Sutherland; A L George; John C Mulley; Samuel F Berkovic
Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.
American journal of human genetics 2001;68(4):859-65.
2001: Samuel F Berkovic; Ingrid E Scheffer
Genetics of the epilepsies.
Epilepsia 2001;42 Suppl 5():16-23.
2001: Regula S Briellmann; Graeme D Jackson; Yvonne Torn-Broers; Samuel F Berkovic
Causes of epilepsies: insights from discordant monozygous twins.
Annals of neurology 2001;49(1):45-52.
2001: Jeffrey V Rosenfeld; A Simon Harvey; Jacquie A Wrennall; Margaret R Zacharin; Samuel F Berkovic
Transcallosal resection of hypothalamic hamartomas, with control of seizures, in children with gelastic epilepsy.
Neurosurgery 2001;48(1):108-18.
2001: Hilary A Phillips; I Favre; Martin Kirkpatrick; Sameer M Zuberi; David R Goudie; Sarah E Heron; Ingrid E Scheffer; Grant R Sutherland; Samuel F Berkovic; D Bertrand; John C Mulley
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy.
American journal of human genetics 2001;68(1):225-31.
2000: Samuel F Berkovic; R Ottman
Molecular genetics of the idiopathic epilepsies: the next steps....
Epileptic disorders : international epilepsy journal with videotape 2000;2(4):179-81.
2000: Regula S Briellmann; Samuel F Berkovic; Graeme D Jackson
Men may be more vulnerable to seizure-associated brain damage.
Neurology 2000;55(10):1479-85.
2000: Regula S Briellmann; Renate M Kalnins; Malcolm Hopwood; C Ward; Samuel F Berkovic; Graeme D Jackson
TLE patients with postictal psychosis: mesial dysplasia and anterior hippocampal preservation.
Neurology 2000;55(7):1027-30.
2000: Paul McCrory; T Ariens; Samuel F Berkovic
The nature and duration of acute concussive symptoms in Australian football.
Clinical journal of sport medicine : official journal of the Canadian Academy of Sport Medicine 2000;10(4):235-8.
2000: S A Ross; John Y F Wong; Jeremiah J Clifford; A Kinsella; Jim S Massalas; Malcolm K Horne; I E Scheffer; I Kola; John L Waddington; Samuel F Berkovic; John Drago
Phenotypic characterization of an alpha 4 neuronal nicotinic acetylcholine receptor subunit knock-out mouse.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2000;20(17):6431-41.
2000: S J Field; Michael M Saling; Samuel F Berkovic
Interictal discourse production in temporal lobe epilepsy.
Brain and language 2000;74(2):213-22.
2000: Regula S Briellmann; Yvonne Torn-Broers; Bridget E Busuttil; BJ Major; Renate M Kalnins; M Olsen; Graeme D Jackson; Albert G Frauman; Samuel F Berkovic
APOE epsilon4 genotype is associated with an earlier onset of chronic temporal lobe epilepsy.
Neurology 2000;55(3):435-7.
2000: Hilary A Phillips; Carla Marini; Ingrid E Scheffer; Grant R Sutherland; John C Mulley; Samuel F Berkovic
A de novo mutation in sporadic nocturnal frontal lobe epilepsy.
Annals of neurology 2000;48(2):264-7.
2000: Amanda G Wood; Michael M Saling; MF O'Shea; Samuel F Berkovic; Graeme D Jackson
Components of verbal learning and hippocampal damage assessed by T2 relaxometry.
Journal of the International Neuropsychological Society : JINS 2000;6(5):529-38.
2000: Ingrid E Scheffer; Robyn H Wallace; John C Mulley; Samuel F Berkovic
Locus for febrile seizures.
Annals of neurology 2000;47(6):840-1.
2000: Josie M Curatolo; Richard A L Macdonell; Samuel F Berkovic; Gavin C A Fabinyi
Intraoperative monitoring to preserve central visual fields during occipital corticectomy for epilepsy.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2000;7(3):234-7.
2000: Paul McCrory; Samuel F Berkovic
Video analysis of acute motor and convulsive manifestations in sport-related concussion.
Neurology 2000;54(7):1488-91.
2000: Jonathan W Sturm; Mark R Newton; Y Chinvarun; Salvatore U Berlangieri; Samuel F Berkovic
Ictal SPECT and interictal PET in the localization of occipital lobe epilepsy.
Epilepsia 2000;41(4):463-6.
2000: Paul McCrory; Samuel F Berkovic; Stephen Cordner
Deaths due to brain injury among footballers in Victoria, 1968-1999.
The Medical journal of Australia 2000;172(5):217-9.
2000: Jonathan W Sturm; Frederick Andermann; Samuel F Berkovic
"Pressure to laugh": an unusual epileptic symptom associated with small hypothalamic hamartomas.
Neurology 2000;54(4):971-3.
2000: Samuel F Berkovic
Familial epilepsies: quality of life issues in genetic research.
Neurology 2000;55(5 Suppl 1):S3-8; discussion S54-8.
2000: Samuel F Berkovic
SPECT: neurobiology of periictal blood flow alterations.
Advances in neurology 2000;83():33-9.
1999: Regula S Briellmann; Graeme D Jackson; L Anne Mitchell; Gregory Fitt; S E Kim; Samuel F Berkovic
Occurrence of hippocampal sclerosis: is one hemisphere or gender more vulnerable?
Epilepsia 1999;40(12):1816-20.
1999: L Xiong; M Labuda; D S Li; Thomas J Hudson; R Desbiens; G Patry; S Verret; P Langevin; Suha Mercho; Marie-Hélène Seni; Ingrid E Scheffer; François Dubeau; Samuel F Berkovic; Frederick Andermann; Eva Andermann; Massimo Pandolfo
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12.
American journal of human genetics 1999;65(6):1698-710.
1999: Graeme D Jackson; B R Chambers; Samuel F Berkovic
Hippocampal sclerosis: development in adult life.
Developmental neuroscience 1999;21(3-5):207-14.
1999: Graeme D Jackson; S E Kim; Gregory Fitt; A L Mitchell; Ari Syngeniotis; Samuel F Berkovic
Hippocampal T(2) abnormalities correlate with antecedent events and help predict seizure intractability.
Developmental neuroscience 1999;21(3-5):200-6.
1999: Richard A L Macdonell; Graeme D Jackson; Josie M Curatolo; David F Abbott; Samuel F Berkovic; Leeanne M Carey; A Syngeniotin; Gavin C A Fabinyi; Ingrid E Scheffer
Motor cortex localization using functional MRI and transcranial magnetic stimulation.
Neurology 1999;53(7):1462-7.
1999: A Brodtmann; Richard A L Macdonell; Amanda K Gilligan; Josie M Curatolo; Samuel F Berkovic
Cortical excitability and recovery curve analysis in generalized epilepsy.
Neurology 1999;53(6):1347-9.
1999: MF O'Shea; Michael M Saling; Samuel F Berkovic
Behavioural status during the intracarotid amobarbital procedure (Wada test): relevance for surgical management.
Journal of neurology, neurosurgery, and psychiatry 1999;67(4):549.
1999: Mark A King; Mark R Newton; Samuel F Berkovic
Benign partial seizures of adolescence.
Epilepsia 1999;40(9):1244-7.
1999: Paul McCrory; Peter F Bladin; Samuel F Berkovic
The cerebellar seizures of Hughlings Jackson.
Neurology 1999;52(9):1888-90.
1999: Rita Singh; Richard A L Macdonell; Ingrid E Scheffer; Kathryn M Crossland; Samuel F Berkovic
Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms.
Epileptic disorders : international epilepsy journal with videotape 1999;1(2):93-9.
1999: Samuel F Berkovic; Ingrid E Scheffer
Genetics of the epilepsies.
Current opinion in neurology 1999;12(2):177-82.
1999: José M Serratosa; Pilar Gómez-Garre; M E Gallardo; B Anta; DB de Bernabé; Dick Lindhout; Paul B Augustijn; Carlo Alberto Tassinari; R M Malafosse; M Topcu; Djamel Grid; Charlotte Dravet; Samuel F Berkovic; Santiago Rodríguez de Córdoba
A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2).
Human molecular genetics 1999;8(2):345-52.
1999: L Anne Mitchell; Graeme D Jackson; Renate M Kalnins; Michael M Saling; Gregory Fitt; R D Ashpole; Samuel F Berkovic
Anterior temporal abnormality in temporal lobe epilepsy: a quantitative MRI and histopathologic study.
Neurology 1999;52(2):327-36.
1999: Samuel F Berkovic; Ortrud K Steinlein
Genetics of partial epilepsies.
Advances in neurology 1999;79():375-81.
1999: Amanda G Wood; Michael M Saling; MF O'Shea; Graeme D Jackson; Samuel F Berkovic
Reorganization of verbal memory and language: a case of dissociation.
Journal of the International Neuropsychological Society : JINS 1999;5(1):69-74.
1999: Rita Singh; Ingrid E Scheffer; Kathryn M Crossland; Samuel F Berkovic
Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome.
Annals of neurology 1999;45(1):75-81.
1998: Regula S Briellmann; Graeme D Jackson; Yvonne Torn-Broers; Samuel F Berkovic
Twins with different temporal lobe malformations: schizencephaly and arachnoid cyst.
Neuropediatrics 1998;29(6):284-8.
1998: Roy G Beran; Samuel F Berkovic; F M Dunagan; Frank J E Vajda; Gytis Danta; A B Black; R Mackenzie
Double-blind, placebo-controlled, crossover study of lamotrigine in treatment-resistant generalised epilepsy.
Epilepsia 1998;39(12):1329-33.
1998: Ingrid E Scheffer; Hilary A Phillips; C E O'Brien; Michael M Saling; Jacquie A Wrennall; Robyn H Wallace; John C Mulley; Samuel F Berkovic
Familial partial epilepsy with variable foci: a new partial epilepsy syndrome with suggestion of linkage to chromosome 2.
Annals of neurology 1998;44(6):890-9.
1998: Regula S Briellmann; Graeme D Jackson; Renate M Kalnins; Samuel F Berkovic
Hemicranial volume deficits in patients with temporal lobe epilepsy with and without hippocampal sclerosis.
Epilepsia 1998;39(11):1174-81.
1998: Hilary A Phillips; Ingrid E Scheffer; Kathryn M Crossland; K P Bhatia; D R Fish; CD Marsden; S J Howell; John B P Stephenson; John Tolmie; G Plazzi; Orvar Eeg-Olofsson; Rita Singh; Iscia Lopes-Cendes; Eva Andermann; Frederick Andermann; Samuel F Berkovic; John C Mulley
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24.
American journal of human genetics 1998;63(4):1108-16.
1998: Mark A King; Mark R Newton; Graeme D Jackson; Gregory Fitt; L Anne Mitchell; M J Silvapulle; Samuel F Berkovic
Epileptology of the first-seizure presentation: a clinical, electroencephalographic, and magnetic resonance imaging study of 300 consecutive patients.
Lancet 1998;352(9133):1007-11.
1998: Samuel F Berkovic; Mark R Newton; A Simon Harvey; Salvatore U Berlangieri
Single photon emission computed tomography-EEG relations in temporal lobe epilepsy.
Neurology 1998;51(2):645-7.
1998: Robyn H Wallace; D W Wang; Rita Singh; Ingrid E Scheffer; A L George; Hilary A Phillips; Kathrin Saar; A Reis; E W Johnson; Grant R Sutherland; Samuel F Berkovic; John C Mulley
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.
Nature genetics 1998;19(4):366-70.
1998: Graeme D Jackson; Anne M McIntosh; Regula S Briellmann; Samuel F Berkovic
Hippocampal sclerosis studied in identical twins.
Neurology 1998;51(1):78-84.
1998: Samuel F Berkovic; Ingrid E Scheffer
Febrile seizures: genetics and relationship to other epilepsy syndromes.
Current opinion in neurology 1998;11(2):129-34.
1998: Samuel F Berkovic; R A Howell; D A Hay; John L Hopper
Epilepsies in twins: genetics of the major epilepsy syndromes.
Annals of neurology 1998;43(4):435-45.
1998: Paul McCrory; Samuel F Berkovic
Second impact syndrome.
Neurology 1998;50(3):677-83.
1998: Paul McCrory; Samuel F Berkovic
Concussive convulsions. Incidence in sport and treatment recommendations.
Sports medicine (Auckland, N.Z.) 1998;25(2):131-6.
1998: Samuel F Berkovic
Aggravation of generalized epilepsies.
Epilepsia 1998;39 Suppl 3():S11-4.
1997: S S Ho; M R Newton; Anne M McIntosh; Renate M Kalnins; Gavin C A Fabinyi; G A Brazenor; WJ McKay; Peter F Bladin; Samuel F Berkovic
Perfusion patterns during temporal lobe seizures: relationship to surgical outcome.
Brain : a journal of neurology 1997;120 ( Pt 11)():1921-8.
1997: M Hayman; Ingrid E Scheffer; Y Chinvarun; Salvatore U Berlangieri; Samuel F Berkovic
Autosomal dominant nocturnal frontal lobe epilepsy: demonstration of focal frontal onset and intrafamilial variation.
Neurology 1997;49(4):969-75.
1997: A Simon Harvey; Samuel F Berkovic; Jacquie A Wrennall; Ian J Hopkins
Temporal lobe epilepsy in childhood: clinical, EEG, and neuroimaging findings and syndrome classification in a cohort with new-onset seizures.
Neurology 1997;49(4):960-8.
1997: Samuel F Berkovic; Ingrid E Scheffer
Genetics of human partial epilepsy.
Current opinion in neurology 1997;10(2):110-4.
1997: Ingrid E Scheffer; Samuel F Berkovic
Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes.
Brain : a journal of neurology 1997;120 ( Pt 3)():479-90.
1997: Paul McCrory; Peter F Bladin; Samuel F Berkovic
Retrospective study of concussive convulsions in elite Australian rules and rugby league footballers: phenomenology, aetiology, and outcome.
BMJ (Clinical research ed.) 1997;314(7075):171-4.
1997: Samuel F Berkovic
Epilepsy genes and the genetics of epilepsy syndromes: the promise of new therapies based on genetic knowledge.
Epilepsia 1997;38 Suppl 9():S32-6.
1997: Samuel F Berkovic; Ingrid E Scheffer
Epilepsies with single gene inheritance.
Brain & development 1997;19(1):13-8.
1997: Terence J O'Brien; Mark R Newton; M J Cook; Salvatore U Berlangieri; Christine Kilpatrick; K Morris; Samuel F Berkovic
Hippocampal atrophy is not a major determinant of regional hypometabolism in temporal lobe epilepsy.
Epilepsia 1997;38(1):74-80.