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Neuromuscular Disorders : NMD|January 1, 1992
Chronic myopathy in a patient suspected of carrying two malignant hyperthermia susceptibility (MHS) mutationsT Deufel, W Müller-Felber, D E Pongratz, et al.Human Molecular Genetics|July 1, 1993
Exclusion of malignant hyperthermia susceptibility (MHS) from a putative MHS2 locus on chromosome 17q and of the alpha 1, beta 1, and gamma subunits of the dihydropyridine receptor calcium channel as candidates for the molecular defectR Sudbrak, A Golla, K Hogan, et al.Neuroscience Letters|August 16, 1996
Role in fast inactivation of conserved amino acids in the IV/S4-S5 loop of the human muscle Na+ channelN Mitrovic, H Lerche, R Heine, et al.The Journal of Physiology|January 21, 2006
A possible role of the junctional face protein JP-45 in modulating Ca2+ release in skeletal muscleE Gouadon, R P Schuhmeier, D Ursu, et al.Archives of Neurology|January 1, 1995
Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophyK Ricker, M C Koch, F Lehmann-Horn, et al.Water Science and Technology : a Journal of the International Association on Water Pollution Research|November 26, 2009
A traditional first flush assessment of E. coli in urban stormwater runoffD T McCarthyCurrent Opinion in Nephrology and Hypertension|November 1, 1996
Renal replacement therapy in acute renal failureJ T McCarthyCurrent Medical Research and Opinion|January 1, 1982
Body fluid, electrolytes and diureticsS T McCarthyMayo Clinic Proceedings|February 1, 1996
Prognosis of patients with acute renal failure in the intensive-care unit: a tale of two erasJ T McCarthyMayo Clinic Proceedings|March 25, 1999
A practical approach to the management of patients with chronic renal failureJ T McCarthyPageof 56