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European Journal of Neurology|October 4, 2020
Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersenV A Sansone, G Coratti, M C Pera, et al.Neurology|May 23, 2007
Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesiaM K Bruno, H-Y Lee, G W J Auburger, et al.Journal of Virology|February 8, 2019
Early Human B Cell Response to Ebola Virus in Four U.S. Survivors of InfectionLauren E Williamson, Andrew I Flyak, Nurgun Kose, et al.Plos Pathogens|October 17, 2013
Crystal structure of the Hendra virus attachment G glycoprotein bound to a potent cross-reactive neutralizing human monoclonal antibodyKai Xu, Barry Rockx, Yihu Xie, et al.Neurology|June 16, 2005
Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathyS Lucioli, B Giusti, E Mercuri, et al.Clinical Genetics|April 23, 2016
A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemiaA Torraco, M Bianchi, D Verrigni, et al.Cell|February 28, 2015
Mechanism of human antibody-mediated neutralization of Marburg virusAndrew I Flyak, Philipp A Ilinykh, Charles D Murin, et al.Neurology|October 20, 2010
Pontocerebellar hypoplasia: clinical, pathologic, and genetic studiesD Cassandrini, R Biancheri, A Tessa, et al.Neuromuscular Disorders : NMD|April 17, 2007
The Hammersmith functional score correlates with the SMN2 copy number: a multicentric studyF D Tiziano, E Bertini, S Messina, et al.Clinical Genetics|November 4, 2016
Microcephaly, intractable seizures and developmental delay caused by biallelic variants in TBCD: further delineation of a new chaperone-mediated tubulinopathyB Pode-Shakked, H Barash, L Ziv, et al.Pageof 29