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Neuromuscular Disorders : NMD|February 13, 2001
Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutationsI Mahjneh, G Marconi, K Bushby, et al.
Neuromuscular Disorders : NMD|June 6, 2000
Calpain3 expression during human cardiogenesisF Fougerousse, L V Anderson, A L Delezoide, et al.
Nature Communications|November 25, 2018
Major intensification of Atlantic overturning circulation at the onset of Paleogene greenhouse warmthS J Batenburg, S Voigt, O Friedrich, et al.
Developmental Medicine and Child Neurology|March 1, 1995
Deletion status and intellectual impairment in Duchenne muscular dystrophyK M Bushby, R Appleton, L V Anderson, et al.
International Journal of Molecular Medicine|December 16, 1998
Mosaicism for Charcot-Marie-Tooth disease type 1A: onset in childhood suggests somatic reversion in early developmental stagesB Rautenstrauss, T Liehr, C Fuchs, et al.
Cureus|July 24, 2023
The Safety and Efficacy of Rituximab and Belimumab in Systemic Lupus Erythematosus: A Systematic ReviewNaushad Abid, Sara Manaye, Hamzah Naushad, et al.
Cureus|April 17, 2023
The Growing Epidemic of Diabetes Among the Indigenous Population of Canada: A Systematic ReviewKaaviya Cheran, Chinmayee Murthy, Elisa A Bornemann, et al.
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