E-LIB Suche - Ergebnisse für: Andermann, Frederick

1

Autosomal-dominant adult neuronal ceroid lipofuscinosis cau..:

The Adult NCL Gene Discovery Consortium ; Jedličková, Ivana ; Cadieux-Dion, Maxime...
European Journal of Human Genetics. 28 (2020) 6 - p. 783-789 , 2020

Link: https://doi.org/10.1038/..

2

Duplication 2p16 is associated with perisylvian polymicrogy..:

Amrom, Dina ; Poduri, Annapurna ; Goldman, Jennifer S....
American Journal of Medical Genetics Part A. 179 (2019) 12 - p. 2343-2356 , 2019

Link: https://doi.org/10.1002/..

3

Kufs disease due to mutation ofCLN6: clinical, pathological..:

Berkovic, Samuel F ; Oliver, Karen L ; Canafoglia, Laura...
Brain. 142 (2018) 1 - p. 59-69 , 2018

Link: https://doi.org/10.1093/..

4

Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analys..:

Oliver, Karen L. ; Franceschetti, Silvana ; Milligan, Carol J....
Annals of Neurology. 81 (2017) 5 - p. 677-689 , 2017

Link: https://doi.org/10.1002/..

5

Phenotypic, molecular, functional, and structural aspects o..:

Amrom, Dina ; Brouhard, Gary ; Bechstedt, Susanne...
Neurology. 84 (2015) 14_supplement - p. , 2015

Link: https://doi.org/10.1212/..

6

The histopathology of polymicrogyria: a series of 71 brain ..:

Jansen, Anna C ; Robitaille, Yves ; Honavar, Mrinalini...
Developmental Medicine & Child Neurology. 58 (2015) 1 - p. 39-48 , 2015

Link: https://doi.org/10.1111/..

7

Brivaracetam in Unverricht‐Lundborg disease (EPM1): Results..:

Kälviäinen, Reetta ; Genton, Pierre ; Andermann, Eva...
Epilepsia. 57 (2015) 2 - p. 210-221 , 2015

Link: https://doi.org/10.1111/..

8

Alternating Hemiplegia of Childhood: Retrospective Genetic ..:

Viollet, Louis ; Glusman, Gustavo ; Murphy, Kelley J....
PLOS ONE. 10 (2015) 5 - p. e0127045 , 2015

Link: https://doi.org/10.1371/..

9

Correction: Alternating Hemiplegia of Childhood: Retrospect..:

Viollet, Louis ; Glusman, Gustavo ; Murphy, Kelley J....
PLOS ONE. 10 (2015) 8 - p. e0137370 , 2015

Link: https://doi.org/10.1371/..

10

Familial focal epilepsy with focal cortical dysplasia due t..:

Baulac, Stéphanie ; Ishida, Saeko ; Marsan, Elise...
Annals of Neurology. 77 (2015) 4 - p. 675-683 , 2015

Link: https://doi.org/10.1002/..

11

4. Familial generalized seizures due to LGI1 mutation: Impo..:

Amrom, Dina ; Andermann, Eva ; Andermann, Frederick
Clinical Neurophysiology. 125 (2014) 5 - p. e10-e11 , 2014

Link: https://doi.org/10.1016/..

12

LGI1Mutation Presenting As Idiopathic Generalized Epilepsy:..:

Amrom, Dina ; Andermann, Frederick ; Dahl, Hans Atli.
Neurology. 82 (2014) 10_supplement - p. , 2014

Link: https://doi.org/10.1212/..

13

Rasmussen encephalitis and comorbid autoimmune diseases: A ..:

Amrom, Dina ; Kinay, Demet ; Hart, Yvonne...
Neurology. 83 (2014) 12 - p. 1049-1055 , 2014

Link: https://doi.org/10.1212/..

14

"Mirror EPC": Epilepsia partialis continua shifting sides a..:

Hemb, Marta ; Paglioli, Eliseu ; Dubeau, François...
Neurology. 83 (2014) 16 - p. 1439-1443 , 2014

Link: https://doi.org/10.1212/..

15

Periventricularlaminar Heterotopia (PLH): Characterization ..:

Amrom, Dina ; Fahoum, Firas ; Dubeau, Francois...
Neurology. 82 (2014) 10_supplement - p. , 2014

Link: https://doi.org/10.1212/..