Genetics of Epilepsy in Clinical Practice

par Berkovic, Samuel F.
Publié dans Epilepsy Curr (2015)

Ramsay Hunt syndrome: to bury or to praise.

par Berkovic, S F, Andermann, F
Publié 1990

Ceftazidime encephalopathy: absence status and toxic hallucinations.

par Jackson, G D, Berkovic, S F
Publié 1992

Properties of neuronal nicotinic acetylcholine receptor mutants from humans suffering from autosomal dominant nocturnal frontal lobe epilepsy

par Bertrand, S, Weiland, S, Berkovic, S F, Steinlein, O K, Bertrand, D
Publié 1998

Retrospective study of concussive convulsions in elite Australian rules and rugby league footballers: phenomenology, aetiology, and outcome.

par McCrory, P. R., Bladin, P. F., Berkovic, S. F.
Publié 1997

Basilar artery dissection.

par Berkovic, S F, Spokes, R L, Anderson, R M, Bladin, P F
Publié 1983

LACK OF REPLICATION OF ASSOCIATION BETWEEN SCN1A SNP AND FEBRILE SEIZURES

par Petrovski, S, Scheffer, I E., Sisodiya, S M., O’Brien, T J., Berkovic, S F.
Publié 2009

ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsies

par Bennett, Caitlin A., Petrovski, Slavé, Oliver, Karen L., Berkovic, Samuel F.
Publié dans Neurol Genet (2017)

The “Maternal Effect” on Epilepsy Risk: Analysis of Familial Epilepsies and Reassessment of Prior Evidence

par Ellis, Colin A., Berkovic, Samuel F., Epstein, Michael P., Ottman, Ruth
Publié dans Ann Neurol (2019)

Generalized, Focal, and Combined Epilepsies in Families: New Evidence for Distinct Genetic Factors

par Ellis, Colin A., Ottman, Ruth, Epstein, Michael P., Berkovic, Samuel F.
Publié dans Epilepsia (2020)

Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21.

par Wallace, R H, Berkovic, S F, Howell, R A, Sutherland, G R, Mulley, J C
Publié 1996

NREM Arousal Parasomnias and Their Distinction from Nocturnal Frontal Lobe Epilepsy: A Video EEG Analysis

par Derry, Christopher P., Harvey, A. Simon, Walker, Matthew C., Duncan, John S., Berkovic, Samuel F.
Publié 2009

A New Locus for Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2

par Lopes-Cendes, I., Scheffer, I. E., Berkovic, S. F., Rousseau, M., Andermann, E., Rouleau, G. A.
Publié 2000

Axon initial segment dysfunction in epilepsy

par Wimmer, Verena C, Reid, Christopher A, So, Eva Y-W, Berkovic, Samuel F, Petrou, Steven
Publié 2010

The genetic basis of music ability

par Tan, Yi Ting, McPherson, Gary E., Peretz, Isabelle, Berkovic, Samuel F., Wilson, Sarah J.
Publié 2014

In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery

par Oliver, Karen L., Lukic, Vesna, Freytag, Saskia, Scheffer, Ingrid E., Berkovic, Samuel F., Bahlo, Melanie
Publié dans Neurol Genet (2016)

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies

par Oyrer, Julia, Maljevic, Snezana, Scheffer, Ingrid E., Berkovic, Samuel F., Petrou, Steven, Reid, Christopher A.
Publié dans Pharmacol Rev (2018)

Epilepsy risk in offspring of affected parents; a cohort study of the “maternal effect” in epilepsy

par Dreier, Julie W., Ellis, Colin A., Berkovic, Samuel F., Cotsapas, Chris, Ottman, Ruth, Christensen, Jakob
Publié dans Ann Clin Transl Neurol (2020)

Networks underlying paroxysmal fast activity and slow spike and wave in Lennox-Gastaut syndrome

par Pillay, Neelan, Archer, John S., Badawy, Radwa A.B., Flanagan, Danny F., Berkovic, Samuel F., Jackson, Graeme
Publié 2013

Harnessing Gene Expression Networks to Prioritize Candidate Epileptic Encephalopathy Genes

par Oliver, Karen L., Lukic, Vesna, Thorne, Natalie P., Berkovic, Samuel F., Scheffer, Ingrid E., Bahlo, Melanie
Publié 2014