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Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1995
Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tanglesR W Orrell, A W King, D A Hilton, et al.
Journal of the Royal Society of Medicine|August 1, 1995
Testosterone deficiency myopathyR W Orrell, D F Woodrow, M C Barrett, et al.
Internal Medicine Journal|November 19, 2014
Enteric fever in the Pacific: a regional retrospective study from Auckland, New ZealandR J Lane, D Holland, S McBride, et al.
World Journal of Surgery|March 1, 1990
Percutaneous control of a portacaval H-graft: description of a new device and its initial clinical applicationR C Smith, A R Brown, P C Spencer, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|October 23, 2018
The integration of pharmacology and pathophysiology into locoregional chemotherapy delivery via mass fluid transferR J Lane, N Y Khin, C M Rogan, et al.
Journal of the Neurological Sciences|November 1, 1979
An evaluation of some carrier detection techniques in Duchenne muscular dystrophyR J Lane, P Maskrey, G A Nicholson, et al.
American Journal of Human Genetics|June 23, 1998
Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNAM G Hanna, I P Nelson, S Rahman, et al.
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