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Neuromuscular Disorders : NMD|January 22, 2002
Two amino-acid substitutions in the myelin protein zero gene of a case of Charcot-Marie-Tooth disease associated with light-near dissociationH M E Bienfait, F Baas, A A W M Gabreëls-Festen, et al.
Human Molecular Genetics|July 27, 2001
Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cellsJ C van Deutekom, M Bremmer-Bout, A A Janson, et al.
Brain : a Journal of Neurology|January 23, 2003
Autoimmunoreactivity to Schwann cells in patients with inflammatory neuropathiesMarcel S G Kwa, Ivo N van Schaik, Rosalein R De Jonge, et al.
Glia|May 15, 2002
Expression and distribution of id helix-loop-helix proteins in human astrocytic tumorsDmitri A A Vandeputte, Dirk Troost, Sieger Leenstra, et al.
Neuroscience|May 6, 2014
SGCZ mutations are unlikely to be associated with myoclonus dystoniaK J Peall, K Ritz, A J Waite, et al.
AIDS Patient Care and Stds|December 3, 2014
Patient and provider perspectives on HIV and HIV-related stigma in Dutch health care settingsSarah E Stutterheim, Lenneke Sicking, Ronald Brands, et al.
Frontiers in Pharmacology|September 25, 2020
Barriers and Enablers of Older Patients to Deprescribing of Cardiometabolic Medication: A Focus Group StudyStijn Crutzen, Gert Baas, Jamila Abou, et al.
G3 (Bethesda, Md.)|August 22, 2012
Forward genetic analysis to identify determinants of dopamine signaling in Caenorhabditis elegans using swimming-induced paralysisJ Andrew Hardaway, Shannon L Hardie, Sarah M Whitaker, et al.
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