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Epileptic Disorders : International Epilepsy Journal with Videotape|September 22, 2007
Familial generalized epilepsy in Bulgarian RomaIvailo Tournev, Barbara Royer, Pierre Szepetowski, et al.
Human Molecular Genetics|September 23, 2010
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complexPatrice Roll, Sonja C Vernes, Nadine Bruneau, et al.
BMC Genetics|October 19, 2007
Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areasBarbara Royer, Dinesh C Soares, Paul N Barlow, et al.
American Journal of Human Genetics|January 19, 2002
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouseAnnachiara De Sandre-Giovannoli, Malika Chaouch, Serguei Kozlov, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 19, 2010
Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndromeJacques Rochette, Patrice Roll, Ying-Hui Fu, et al.
Plos One|November 10, 2010
Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11Patrice Roll, Damien Sanlaville, Jennifer Cillario, et al.
Journal of Neuroinflammation|November 16, 2024
Cytomegalovirus infection of the fetal brain: intake of aspirin during pregnancy blunts neurodevelopmental pathogenesis in the offspringSarah Tarhini, Carla Crespo-Quiles, Emmanuelle Buhler, et al.
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