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Revue Neurologique|March 18, 2008
[Hereditary ataxias, spastic parapareses and neuropathies in Eastern Canada]N Dupré, N Chrestian, I Thiffault, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|January 12, 2007
K-Cl cotransport in red blood cells from patients with KCC3 isoform mutantsP K Lauf, N C Adragna, N Dupre, et al.
Fertility and Sterility|May 1, 1992
Cotreatment with growth hormone for induction of spermatogenesis in patients with hypogonadotropic hypogonadismZ Shoham, G S Conway, H Ostergaard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1976
Nerve conduction studies and electromyography in Friedreich's ataxiaJ M Peyronnard, L Lapointe, J P Bouchard, et al.
Genetic Testing|January 15, 2002
Rapid detection of the sacsin mutations causing autosomal recessive spastic ataxia of Charlevoix-SaguenayJ Mercier, C Prévost, J C Engert, et al.
The Journal of Biological Chemistry|July 29, 1994
Phosphorylation and identification of a major tyrosine phosphorylation site in protein tyrosine phosphatase 1CP Bouchard, Z Zhao, D Banville, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1993
Role of estradiol in the rise in follicle-stimulating hormone levels during the luteal-follicular transitionE le Nestour, J Marraoui, N Lahlou, et al.
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