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Revue Neurologique|April 8, 2020
Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adultsY Nadjar, S Souvannanorath, T Maisonobe, et al.
Annales De Cardiologie Et D'Angeiologie|October 30, 1986
[Treatment of unstable angina. A randomized double-blind study of propranolol, diltiazem and molsidomine]G Nicolas, S Witchitz, P Beaufils, et al.
Journal of Neuroendocrinology|February 13, 2025
NETest® 2.0-A decade of innovation in neuroendocrine tumor diagnosticsM Kidd, I A Drozdov, A Chirindel, et al.
Journal of Molecular Neuroscience : MN|January 4, 2012
Proximal giant neurofilamentous axonopathy in mice genetically engineered to resist calpain and caspase cleavage of α-II spectrinR Kassa, V Monterroso, J Wentzell, et al.
Revue Neurologique|August 6, 2025
Homozygous DNAJB4 deletion revealing myopathy with acute respiratory failureD M Chitimus, C Adam, C Cauquil, et al.
Revue Neurologique|May 8, 2009
[Update on fundamental and clinical research in amyotrophic lateral sclerosis]P-F Pradat, J-P Camdessanché, L Carluer, et al.
Clinical Lymphoma, Myeloma & Leukemia|June 1, 2010
Feasibility of therapy with hypomethylating agents in patients with renal insufficiencyG Nicolas Batty, Hagop Kantarjian, Jean-Pierre Issa, et al.
Revue Neurologique|May 18, 2010
[Research in amyotrophic lateral sclerosis: what is new in 2009?]P-F Pradat, S Attarian, J-P Camdessanché, et al.
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