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Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core diseaseP J Lynch, J Tong, M Lehane, et al.Human Molecular Genetics|October 1, 1994
Detection of a novel RYR1 mutation in four malignant hyperthermia pedigreesK E Keating, K A Quane, B M Manning, et al.Human Molecular Genetics|March 1, 1994
Detection of a novel common mutation in the ryanodine receptor gene in malignant hyperthermia: implications for diagnosis and heterogeneity studiesK A Quane, K E Keating, B M Manning, et al.Anesthesia and Analgesia|January 7, 2000
A multicenter study of 4-chloro-m-cresol for diagnosing malignant hyperthermia susceptibilityC P Baur, L Bellon, P Felleiter, et al.American Journal of Human Genetics|April 29, 1998
Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlationB M Manning, K A Quane, H Ording, et al.Acta Anaesthesiologica Scandinavica|October 6, 1997
In vitro contracture test for diagnosis of malignant hyperthermia following the protocol of the European MH Group: results of testing patients surviving fulminant MH and unrelated low-risk subjects. The European Malignant Hyperthermia GroupH Ording, V Brancadoro, S Cozzolino, et al.Pageof 7