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I E Scheffer

Showing results (21-30 of 75) with videos related to

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Epileptic Disorders : International Epilepsy Journal with Videotape|August 11, 2000
Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanismsR Singh, R A Macdonell, I E Scheffer, et al.
Neuropediatrics|May 1, 1991
Pelizaeus-Merzbacher disease: classical or connatal?I E Scheffer, M Baraitser, J Wilson, et al.
Neurology|June 25, 2010
Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiencyS A Mullen, A Suls, P De Jonghe, et al.
Neurology|December 2, 2009
Lack of replication of association between scn1a SNP and febrile seizuresS Petrovski, I E Scheffer, S M Sisodiya, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 22, 2008
How long should a routine EEG be?K A Reardon, I E Scheffer, L J Smith, et al.
American Journal of Human Genetics|March 21, 2000
A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2I Lopes-Cendes, I E Scheffer, S F Berkovic, et al.
Annals of Neurology|October 1, 1995
Autosomal dominant rolandic epilepsy and speech dyspraxia: a new syndrome with anticipationI E Scheffer, L Jones, M Pozzebon, et al.
Annals of Neurology|August 12, 2000
A de novo mutation in sporadic nocturnal frontal lobe epilepsyH A Phillips, C Marini, I E Scheffer, et al.
Neurology|April 13, 2005
Amygdala dysplasia with temporal lobe epilepsy and obsessive-compulsive disorder: an fMRI/EEG studyA Labate, R S Briellmann, I E Scheffer, et al.
Archives of Neurology|November 1, 1994
Phenotypic expression of benign familial neonatal convulsions linked to chromosome 20S F Berkovic, M L Kennerson, R A Howell, et al.
Pageof 8

Showing results (21-30 of 75) with videos related to

Sort By:
Pageof 8
Epileptic Disorders : International Epilepsy Journal with Videotape|August 11, 2000
Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanismsR Singh, R A Macdonell, I E Scheffer, et al.
Neuropediatrics|May 1, 1991
Pelizaeus-Merzbacher disease: classical or connatal?I E Scheffer, M Baraitser, J Wilson, et al.
Neurology|June 25, 2010
Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiencyS A Mullen, A Suls, P De Jonghe, et al.
Neurology|December 2, 2009
Lack of replication of association between scn1a SNP and febrile seizuresS Petrovski, I E Scheffer, S M Sisodiya, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 22, 2008
How long should a routine EEG be?K A Reardon, I E Scheffer, L J Smith, et al.
American Journal of Human Genetics|March 21, 2000
A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2I Lopes-Cendes, I E Scheffer, S F Berkovic, et al.
Annals of Neurology|October 1, 1995
Autosomal dominant rolandic epilepsy and speech dyspraxia: a new syndrome with anticipationI E Scheffer, L Jones, M Pozzebon, et al.
Annals of Neurology|August 12, 2000
A de novo mutation in sporadic nocturnal frontal lobe epilepsyH A Phillips, C Marini, I E Scheffer, et al.
Neurology|April 13, 2005
Amygdala dysplasia with temporal lobe epilepsy and obsessive-compulsive disorder: an fMRI/EEG studyA Labate, R S Briellmann, I E Scheffer, et al.
Archives of Neurology|November 1, 1994
Phenotypic expression of benign familial neonatal convulsions linked to chromosome 20S F Berkovic, M L Kennerson, R A Howell, et al.
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