These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
121 related articles for article (PubMed ID: 7586638)
21. Screening of the ryanodine receptor gene in 105 malignant hyperthermia families: novel mutations and concordance with the in vitro contracture test. Brandt A; Schleithoff L; Jurkat-Rott K; Klingler W; Baur C; Lehmann-Horn F Hum Mol Genet; 1999 Oct; 8(11):2055-62. PubMed ID: 10484775 [TBL] [Abstract][Full Text] [Related]
22. North American malignant hyperthermia population: screening of the ryanodine receptor gene and identification of novel mutations. Sambuughin N; Sei Y; Gallagher KL; Wyre HW; Madsen D; Nelson TE; Fletcher JE; Rosenberg H; Muldoon SM Anesthesiology; 2001 Sep; 95(3):594-9. PubMed ID: 11575529 [TBL] [Abstract][Full Text] [Related]
23. The genetic basis of malignant hyperthermia. Moochhala SM; Tan WT; Lee TL Ann Acad Med Singap; 1994 Jul; 23(4):475-8. PubMed ID: 7979121 [TBL] [Abstract][Full Text] [Related]
24. Determination of a positive malignant hyperthermia (MH) disposition without the in vitro contracture test in families carrying the RYR1 Arg614Cys mutation. Rueffert H; Olthoff D; Deutrich C; Froster UG Clin Genet; 2001 Aug; 60(2):117-24. PubMed ID: 11553045 [TBL] [Abstract][Full Text] [Related]
25. Identification of genetic mutations in Australian malignant hyperthermia families using sequencing of RYR1 hotspots. Gillies RL; Bjorksten AR; Davis M; Du Sart D Anaesth Intensive Care; 2008 May; 36(3):391-403. PubMed ID: 18564801 [TBL] [Abstract][Full Text] [Related]
26. Discordance, in a malignant hyperthermia pedigree, between in vitro contracture-test phenotypes and haplotypes for the MHS1 region on chromosome 19q12-13.2, comprising the C1840T transition in the RYR1 gene. Deufel T; Sudbrak R; Feist Y; Rübsam B; Du Chesne I; Schäfer KL; Roewer N; Grimm T; Lehmann-Horn F; Hartung EJ Am J Hum Genet; 1995 Jun; 56(6):1334-42. PubMed ID: 7762556 [TBL] [Abstract][Full Text] [Related]
27. A cysteine-for-arginine substitution (R614C) in the human skeletal muscle calcium release channel cosegregates with malignant hyperthermia. Hogan K; Couch F; Powers PA; Gregg RG Anesth Analg; 1992 Sep; 75(3):441-8. PubMed ID: 1510267 [TBL] [Abstract][Full Text] [Related]
28. Mutation screening of the RYR1-cDNA from peripheral B-lymphocytes in 15 Swedish malignant hyperthermia index cases. Broman M; Gehrig A; Islander G; Bodelsson M; Ranklev-Twetman E; Rüffert H; Müller CR Br J Anaesth; 2009 May; 102(5):642-9. PubMed ID: 19346234 [TBL] [Abstract][Full Text] [Related]
29. Discordance between malignant hyperthermia susceptibility and RYR1 mutation C1840T in two Scandinavian MH families exhibiting this mutation. Fagerlund TH; Ording H; Bendixen D; Islander G; Ranklev Twetman E; Berg K Clin Genet; 1997 Dec; 52(6):416-21. PubMed ID: 9520251 [TBL] [Abstract][Full Text] [Related]
30. Identification of heterozygous and homozygous individuals with the novel RYR1 mutation Cys35Arg in a large kindred. Lynch PJ; Krivosic-Horber R; Reyford H; Monnier N; Quane K; Adnet P; Haudecoeur G; Krivosic I; McCarthy T; Lunardi J Anesthesiology; 1997 Mar; 86(3):620-6. PubMed ID: 9066328 [TBL] [Abstract][Full Text] [Related]
31. A case of discordance between genotype and phenotype in a malignant hyperthermia family. Fortunato G; Carsana A; Tinto N; Brancadoro V; Canfora G; Salvatore F Eur J Hum Genet; 1999; 7(4):415-20. PubMed ID: 10352931 [TBL] [Abstract][Full Text] [Related]
32. No C1840 to T mutation in RYR1 in malignant hyperthermia. Hall-Curran JL; Stewart AD; Ball SP; Halsall JP; Hopkins PM; Ellis FR Hum Mutat; 1993; 2(4):330. PubMed ID: 8401544 [No Abstract] [Full Text] [Related]
33. Malignant hyperthermia susceptibility in a patient with concomitant motor neuron disease. Monsieurs KG; Van Broeckhoven C; Martin JJ; Dehaene I; Heytens LG J Neurol Sci; 1996 Oct; 142(1-2):36-8. PubMed ID: 8902717 [TBL] [Abstract][Full Text] [Related]
34. The role of the skeletal muscle ryanodine receptor gene in malignant hyperthermia. MacLennan DH; Otsu K; Fujii J; Zorzato F; Phillips MS; O'Brien PJ; Archibald AL; Britt BA; Gillard EF; Worton RG Symp Soc Exp Biol; 1992; 46():189-201. PubMed ID: 1341035 [TBL] [Abstract][Full Text] [Related]
35. Malignant hyperthermia in Japan: mutation screening of the entire ryanodine receptor type 1 gene coding region by direct sequencing. Ibarra M CA; Wu S; Murayama K; Minami N; Ichihara Y; Kikuchi H; Noguchi S; Hayashi YK; Ochiai R; Nishino I Anesthesiology; 2006 Jun; 104(6):1146-54. PubMed ID: 16732084 [TBL] [Abstract][Full Text] [Related]
37. Mutation screening in the ryanodine receptor 1 gene (RYR1) in patients susceptible to malignant hyperthermia who show definite IVCT results: identification of three novel mutations. Rueffert H; Olthoff D; Deutrich C; Meinecke CD; Froster UG Acta Anaesthesiol Scand; 2002 Jul; 46(6):692-8. PubMed ID: 12059893 [TBL] [Abstract][Full Text] [Related]
38. Functional properties of RYR1 mutations identified in Swedish patients with malignant hyperthermia and central core disease. Vukcevic M; Broman M; Islander G; Bodelsson M; Ranklev-Twetman E; Müller CR; Treves S Anesth Analg; 2010 Jul; 111(1):185-90. PubMed ID: 20142353 [TBL] [Abstract][Full Text] [Related]
39. A mutation in the human ryanodine receptor gene associated with central core disease. Zhang Y; Chen HS; Khanna VK; De Leon S; Phillips MS; Schappert K; Britt BA; Browell AK; MacLennan DH Nat Genet; 1993 Sep; 5(1):46-50. PubMed ID: 8220422 [TBL] [Abstract][Full Text] [Related]
40. Mutations to Gly2370, Gly2373 or Gly2375 in malignant hyperthermia domain 2 decrease caffeine and cresol sensitivity of the rabbit skeletal-muscle Ca2+-release channel (ryanodine receptor isoform 1). Du GG; Oyamada H; Khanna VK; MacLennan DH Biochem J; 2001 Nov; 360(Pt 1):97-105. PubMed ID: 11695996 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]