Showing results (161-170 of 221) with videos related to

Sort By:
Pageof 23
The Science of the Total Environment|January 17, 2024
Drought legacy interacts with wildfire to alter soil microbial communities in a Mediterranean climate-type forestA J M Hopkins, A J Brace, J L Bruce, et al.
Brain : a Journal of Neurology|May 17, 2001
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4AD Sternberg, T Maisonobe, K Jurkat-Rott, et al.
Neuromuscular Disorders : NMD|January 1, 1995
Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegiaB Fontaine, C S Rime, J Hazan, et al.
American Journal of Physiology. Cell Physiology|July 3, 2009
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubesS Sacconi, D Simkin, N Arrighi, et al.
Cardiovascular and Interventional Radiology|November 4, 2000
Retrospective comparison of the patency of Wallstents and Palmaz long-medium stents used for TIPS. Transjugular intrahepatic portosystemic shuntsJ J Borsa, A B Fontaine, E K Hoffer, et al.
Neuromuscular Disorders : NMD|August 5, 2014
Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotoniaA Furby, S Vicart, J P Camdessanché, et al.
Journal of Vascular and Interventional Radiology : JVIR|July 1, 1994
Decreased platelet adherence of polymer-coated tantalum stentsA B Fontaine, K Koelling, J Clay, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1994
Dementia in two histologically confirmed cases of multiple sclerosis: one case with isolated dementia and one case associated with psychiatric symptomsB Fontaine, D Seilhean, A Tourbah, et al.
Nature Genetics|March 1, 1994
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European familiesB Fontaine, J Vale-Santos, K Jurkat-Rott, et al.
Pageof 23