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Neuromuscular Disorders : NMD|March 6, 2007
A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complexHeather MacLeod, Peter Pytel, Robert Wollmann, et al.Annals of Neurology|June 3, 2004
Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutationKathryn J Swoboda, Emmanuel Kanavakis, Athina Xaidara, et al.Pediatrics|March 4, 2009
Alternating hemiplegia of childhood: early characteristics and evolution of a neurodevelopmental syndromeMatthew T Sweney, Kenneth Silver, Marion Gerard-Blanluet, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 9, 2018
Benign nocturnal alternating hemiplegia of childhood: A clinical and nomenclatural reappraisalRoderick P P W M Maas, Erik-Jan Kamsteeg, Salvatore Mangano, et al.Archives of Neurology|November 14, 2007
Sanfilippo syndrome type D: natural history and identification of 3 novel mutations in the GNS GeneAn C M Jansen, Henian Cao, Paige Kaplan, et al.Archives of Physical Medicine and Rehabilitation|September 24, 2020
Managing the Rehabilitation Wave: Rehabilitation Services for COVID-19 SurvivorsSoo Y Kim, Sowmya Kumble, Bhavesh Patel, et al.Neurology. Genetics|March 16, 2017
Research conference summary from the 2014 International Task Force on ATP1A3-Related DisordersHendrik Rosewich, Matthew T Sweney, Suzanne DeBrosse, et al.Plos One|May 22, 2015
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF RegistryLouis Viollet, Gustavo Glusman, Kelley J Murphy, et al.Nature Genetics|July 31, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodErin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, et al.Pageof 2