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Annals of Neurology|April 21, 2007
C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathyVirginie Carmignac, Mustafa A M Salih, Susana Quijano-Roy, et al.Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|January 24, 2019
Assessing baloxavir susceptibility of influenza viruses circulating in the United States during the 2016/17 and 2017/18 seasonsLarisa V Gubareva, Vasiliy P Mishin, Mira C Patel, et al.Frontiers in Oncology|December 20, 2024
A 16-week progressive exercise training intervention in treatment-naïve chronic lymphocytic leukaemia: a randomised-controlled pilot studyFrankie F Brown, Rebecca Oliver, Rachel Eddy, et al.The Journal of Infectious Diseases|September 30, 2025
Respiratory Virus Infections and Pulmonary Impairment after Allogeneic Hematopoietic Cell TransplantationGuang-Shing Cheng, Angela P Campbell, Hu Xie, et al.Neurology|May 1, 1997
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyB Eymard, N B Romero, F Leturcq, et al.Brain Pathology (Zurich, Switzerland)|August 12, 2008
A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severityCecilia Jimenez-Mallebrera, Silvia Torelli, Lucy Feng, et al.Kidney International|September 6, 2000
Effect of hemoglobin levels in hemodialysis patients with asymptomatic cardiomyopathyR N Foley, P S Parfrey, J Morgan, et al.Journal of Medical Genetics|June 1, 1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.Elife|May 1, 2016
The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan additionJeremy L Praissman, Tobias Willer, M Osman Sheikh, et al.BMC Bioinformatics|February 26, 2014
Toolboxes for a standardised and systematic study of glycansMatthew P Campbell, René Ranzinger, Thomas Lütteke, et al.Pageof 129