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PUBMED FOR HANDHELDS

Journal Abstract Search

249 related items for PubMed ID: 23628358

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  • 3. The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations.
    Knuiman GJ, Küsters B, Eshuis L, Snoeck M, Lammens M, Heytens L, De Ridder W, Baets J, Scalco RS, Quinlivan R, Holton J, Bodi I, Wraige E, Radunovic A, von Landenberg C, Reimann J, Kamsteeg EJ, Sewry C, Jungbluth H, Voermans NC.
    J Neurol; 2019 Apr; 266(4):876-887. PubMed ID: 30788618
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  • 9. Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndrome.
    Witting N, Laforêt P, Voermans NC, Roux-Buisson N, Bompaire F, Rendu J, Duno M, Feillet F, Kamsteeg EJ, Poulsen NS, Dahlqvist JR, Romero NB, Fauré J, Vissing J, Behin A.
    Acta Neurol Scand; 2018 May; 137(5):452-461. PubMed ID: 29635721
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  • 10. Exertional Heat Stroke and Susceptibility to Malignant Hyperthermia in an Athlete: Evidence for a Link?
    Poussel M, Guerci P, Kaminsky P, Heymonet M, Roux-Buisson N, Faure J, Fronzaroli E, Chenuel B.
    J Athl Train; 2015 Nov; 50(11):1212-4. PubMed ID: 26565425
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  • 11. The neuromuscular and multisystem features of RYR1-related malignant hyperthermia and rhabdomyolysis: A study protocol.
    van den Bersselaar LR, Kruijt N, Scheffer GJ, van Eijk L, Malagon I, Buckens S, Custers JA, Helder L, Greco A, Joosten LA, van Engelen BG, van Alfen N, Riazi S, Treves S, Jungbluth H, Snoeck MM, Voermans NC.
    Medicine (Baltimore); 2021 Aug 20; 100(33):e26999. PubMed ID: 34414986
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  • 13. Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathy.
    Kraeva N, Heytens L, Jungbluth H, Treves S, Voermans N, Kamsteeg E, Ceuterick-de Groote C, Baets J, Riazi S.
    Neuromuscul Disord; 2015 Jul 20; 25(7):567-76. PubMed ID: 25958340
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  • 15. Muscle Ultrasound Abnormalities in Individuals with RYR1-Related Malignant Hyperthermia Susceptibility.
    van den Bersselaar LR, van Alfen N, Kruijt N, Kamsteeg EJ, Fernandez-Garcia MA, Treves S, Riazi S, Yang CY, Malagon I, van Eijk LT, van Engelen BGM, Scheffer GJ, Jungbluth H, Snoeck MMJ, Voermans NC.
    J Neuromuscul Dis; 2023 Jul 20; 10(4):541-554. PubMed ID: 37154182
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  • 17. RYR1 mutations causing central core disease are associated with more severe malignant hyperthermia in vitro contracture test phenotypes.
    Robinson RL, Brooks C, Brown SL, Ellis FR, Halsall PJ, Quinnell RJ, Shaw MA, Hopkins PM.
    Hum Mutat; 2002 Aug 20; 20(2):88-97. PubMed ID: 12124989
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  • 18. 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 20; 95(3):594-9. PubMed ID: 11575529
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  • 19. Structural changes and contractility in muscle assessed by magnetic resonance imaging in individuals with ryanodine receptor 1-related rhabdomyolysis or myalgia.
    Lyu Z, Solheim TÅ, Poulsen NS, Eisum AV, Beha GH, Fornander F, Andersen AG, Witting N, Vissing J.
    Muscle Nerve; 2024 Oct 20; 70(4):753-760. PubMed ID: 39045890
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  • 20. Genetic variation in RYR1 and malignant hyperthermia phenotypes.
    Carpenter D, Robinson RL, Quinnell RJ, Ringrose C, Hogg M, Casson F, Booms P, Iles DE, Halsall PJ, Steele DS, Shaw MA, Hopkins PM.
    Br J Anaesth; 2009 Oct 20; 103(4):538-48. PubMed ID: 19648156
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