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Journal Abstract Search

139 related items for PubMed ID: 8828983

  • 21.
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  • 24. Recombination between the postulated CCD/MHE/MHS locus and RYR1 gene markers.
    Fagerlund TH, Islander G, Ranklev-Twetman E, Berg K.
    Clin Genet; 1996 Dec; 50(6):455-8. PubMed ID: 9147872
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  • 25. Malignant hyperthermia and central core disease causative mutations in Swedish patients.
    Broman M, Islander G, Müller CR, Ranklev-Twetman E.
    Acta Anaesthesiol Scand; 2007 Jan; 51(1):50-3. PubMed ID: 17081152
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  • 27. Malignant hyperthermia susceptibility in patients with exertional rhabdomyolysis: a retrospective cohort study and updated systematic review.
    Kraeva N, Sapa A, Dowling JJ, Riazi S.
    Can J Anaesth; 2017 Jul; 64(7):736-743. PubMed ID: 28326467
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  • 29. [Biology of malignant hyperthermia: a disease of the calcium channels of the skeletal muscle].
    Monnier N, Lunardi J.
    Ann Biol Clin (Paris); 2000 Jul; 58(2):147-56. PubMed ID: 10760701
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  • 30. Localization of the gene encoding the alpha 2/delta-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families.
    Iles DE, Lehmann-Horn F, Scherer SW, Tsui LC, Olde Weghuis D, Suijkerbuijk RF, Heytens L, Mikala G, Schwartz A, Ellis FR.
    Hum Mol Genet; 1994 Jun; 3(6):969-75. PubMed ID: 7951247
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  • 31. 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
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  • 33. 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
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  • 35. 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
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  • 38. Phenotypes associated with malignant hyperthermia susceptibility in swine genotyped as homozygous or heterozygous for the ryanodine receptor mutation.
    Fletcher JE, Calvo PA, Rosenberg H.
    Br J Anaesth; 1993 Sep; 71(3):410-7. PubMed ID: 8398525
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  • 39. Correlations between genotype and pharmacological, histological, functional, and clinical phenotypes in malignant hyperthermia susceptibility.
    Monnier N, Kozak-Ribbens G, Krivosic-Horber R, Nivoche Y, Qi D, Kraev N, Loke J, Sharma P, Tegazzin V, Figarella-Branger D, Roméro N, Mezin P, Bendahan D, Payen JF, Depret T, Maclennan DH, Lunardi J.
    Hum Mutat; 2005 Nov; 26(5):413-25. PubMed ID: 16163667
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  • 40. Molecular genetic detection of susceptibility to malignant hyperthermia in Belgian families.
    Heytens L.
    Acta Anaesthesiol Belg; 2007 Nov; 58(2):113-8. PubMed ID: 17710899
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