Showing results (571-580 of 1,657) with videos related to
Sort By:
Pageof 166
Journal of Applied Physiology (Bethesda, Md. : 1985)|October 12, 2023
Supporting evidence for an "arterial pump" venous return mechanism in humansJeremy N Cohen, Rose A Samra, Jason S AuDigestive Diseases and Sciences|January 1, 1989
Chlamydial ascitesR C Guagenti, A L Berman, N N CohenJournal of Medical Genetics|November 1, 1994
Deletions in the 5' region of dystrophin and resulting phenotypesF Muntoni, P Gobbi, C Sewry, et al.Bone|September 30, 2004
The relationship between lean body mass and bone mineral content in paediatric health and diseaseN J Crabtree, M S Kibirige, J N Fordham, et al.Journal of Submicroscopic Cytology and Pathology|July 1, 1997
Immunolocalization of several laminin chains in the normal human central and peripheral nervous systemM Villanova, C Sewry, A Malandrini, et al.Neuropediatrics|November 10, 2004
Short-chain acyl-CoA dehydrogenase deficiency associated with early onset severe axonal neuropathyM A Kurian, L Hartley, Z Zolkipli, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 30, 2007
Predictive factors for the development of scoliosis in Duchenne muscular dystrophyM Kinali, M Main, J Eliahoo, et al.Neuropediatrics|June 1, 1995
Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophyT Voit, C A Sewry, K Meyer, et al.Neuromuscular Disorders : NMD|June 3, 1998
Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophyF Muntoni, E J Lichtarowicz-Krynska, C A Sewry, et al.Neuromuscular Disorders : NMD|November 2, 1999
Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndromeB Moghadaszadeh, H Topaloglu, L Merlini, et al.Pageof 166