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Journal of the Neurological Sciences|October 1, 1996
Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel geneE Plassart, B Eymard, L Maurs, et al.The Journal of Physiology|March 1, 1995
Skeletal muscle DHP receptor mutations alter calcium currents in human hypokalaemic periodic paralysis myotubesI Sipos, K Jurkat-Rott, C Harasztosi, et al.Journal of Inherited Metabolic Disease|March 18, 2008
Leukoencephalopathies associated with inborn errors of metabolism in adultsF Sedel, A Tourbah, B Fontaine, et al.Diabetologia|June 24, 2010
Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish populationB Fontaine-Bisson, F Renström, O Rolandsson, et al.Journal of Vascular and Interventional Radiology : JVIR|October 5, 2001
Peripherally inserted central catheters with distal versus proximal valves: prospective randomized trialE K Hoffer, R D Bloch, J J Borsa, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 16, 1997
Renal artery dissection causing renal infarction in otherwise healthy menA Alamir, D F Middendorf, P Baker, et al.Neurology|July 1, 1994
The phenotype of "pure" autosomal dominant spastic paraplegiaA Dürr, A Brice, M Serdaru, et al.American Journal of Human Genetics|March 21, 2000
A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34B Fontaine, C S Davoine, A Dürr, et al.Revue Neurologique|March 12, 2002
[Andermann syndrome in an Algerian family: suggestion of phenotype and genetic homogeneity]G Lesca, I Cournu-Rebeix, A Azoulay-Cayla, et al.Revue Neurologique|May 2, 2002
[Acute optic neuritis: clinical and MRI prognostic factors. Study of fifty patients]R Deschamps, O Gout, B Fontaine, et al.Pageof 23