210 related articles for article (PubMed ID: 27663056)
1. RYR1-related rhabdomyolysis: A common but probably underdiagnosed manifestation of skeletal muscle ryanodine receptor dysfunction.
Voermans NC; Snoeck M; Jungbluth H
Rev Neurol (Paris); 2016 Oct; 172(10):546-558. PubMed ID: 27663056
[TBL] [Abstract][Full Text] [Related]
2. Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis.
Dlamini N; Voermans NC; Lillis S; Stewart K; Kamsteeg EJ; Drost G; Quinlivan R; Snoeck M; Norwood F; Radunovic A; Straub V; Roberts M; Vrancken AF; van der Pol WL; de Coo RI; Manzur AY; Yau S; Abbs S; King A; Lammens M; Hopkins PM; Mohammed S; Treves S; Muntoni F; Wraige E; Davis MR; van Engelen B; Jungbluth H
Neuromuscul Disord; 2013 Jul; 23(7):540-8. PubMed ID: 23628358
[TBL] [Abstract][Full Text] [Related]
3. 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
[TBL] [Abstract][Full Text] [Related]
4. RYR1-Related Rhabdomyolysis: A Spectrum of Hypermetabolic States Due to Ryanodine Receptor Dysfunction.
Kruijt N; den Bersselaar LV; Snoeck M; Kramers K; Riazi S; Bongers C; Treves S; Jungbluth H; Voermans N
Curr Pharm Des; 2022; 28(1):2-14. PubMed ID: 34348614
[TBL] [Abstract][Full Text] [Related]
5. RYR1-related myopathies: a wide spectrum of phenotypes throughout life.
Snoeck M; van Engelen BG; Küsters B; Lammens M; Meijer R; Molenaar JP; Raaphorst J; Verschuuren-Bemelmans CC; Straathof CS; Sie LT; de Coo IF; van der Pol WL; de Visser M; Scheffer H; Treves S; Jungbluth H; Voermans NC; Kamsteeg EJ
Eur J Neurol; 2015 Jul; 22(7):1094-112. PubMed ID: 25960145
[TBL] [Abstract][Full Text] [Related]
6. The ryanodine receptor type 1 gene variants in African American men with exertional rhabdomyolysis and malignant hyperthermia susceptibility.
Sambuughin N; Capacchione J; Blokhin A; Bayarsaikhan M; Bina S; Muldoon S
Clin Genet; 2009 Dec; 76(6):564-8. PubMed ID: 19807743
[TBL] [Abstract][Full Text] [Related]
7. 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
[TBL] [Abstract][Full Text] [Related]
8. 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
[TBL] [Abstract][Full Text] [Related]
9. Strenuous exercise triggers a life-threatening response in mice susceptible to malignant hyperthermia.
Michelucci A; Paolini C; Boncompagni S; Canato M; Reggiani C; Protasi F
FASEB J; 2017 Aug; 31(8):3649-3662. PubMed ID: 28465322
[TBL] [Abstract][Full Text] [Related]
10. 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; 100(33):e26999. PubMed ID: 34414986
[TBL] [Abstract][Full Text] [Related]
11. Exercise-induced rhabdomyolysis and stress-induced malignant hyperthermia events, association with malignant hyperthermia susceptibility, and RYR1 gene sequence variations.
Carsana A
ScientificWorldJournal; 2013; 2013():531465. PubMed ID: 23476141
[TBL] [Abstract][Full Text] [Related]
12. Neuromuscular symptoms in patients with
van den Bersselaar LR; Jungbluth H; Kruijt N; Kamsteeg EJ; Fernandez-Garcia MA; Treves S; Riazi S; Malagon I; van Eijk LT; van Alfen N; van Engelen BGM; Scheffer GJ; Snoeck MMJ; Voermans NC
Brain Commun; 2022; 4(6):fcac292. PubMed ID: 36751502
[TBL] [Abstract][Full Text] [Related]
13. Calcium regulation by skeletal muscle membranes of horses with recurrent exertional rhabdomyolysis.
Ward TL; Valberg SJ; Gallant EM; Mickelson JR
Am J Vet Res; 2000 Mar; 61(3):242-7. PubMed ID: 10714513
[TBL] [Abstract][Full Text] [Related]
14. A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene.
Løseth S; Voermans NC; Torbergsen T; Lillis S; Jonsrud C; Lindal S; Kamsteeg EJ; Lammens M; Broman M; Dekomien G; Maddison P; Muntoni F; Sewry C; Radunovic A; de Visser M; Straub V; van Engelen B; Jungbluth H
J Neurol; 2013 Jun; 260(6):1504-10. PubMed ID: 23329375
[TBL] [Abstract][Full Text] [Related]
15. Ryanodine receptor mutations in malignant hyperthermia and central core disease.
McCarthy TV; Quane KA; Lynch PJ
Hum Mutat; 2000; 15(5):410-7. PubMed ID: 10790202
[TBL] [Abstract][Full Text] [Related]
16. 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
[TBL] [Abstract][Full Text] [Related]
17. Investigating the genetic susceptibility to exertional heat illness.
Gardner L; Miller DM; Daly C; Gupta PK; House C; Roiz de Sa D; Shaw MA; Hopkins PM
J Med Genet; 2020 Aug; 57(8):531-541. PubMed ID: 32054689
[TBL] [Abstract][Full Text] [Related]
18. Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene.
Jungbluth H; Zhou H; Hartley L; Halliger-Keller B; Messina S; Longman C; Brockington M; Robb SA; Straub V; Voit T; Swash M; Ferreiro A; Bydder G; Sewry CA; Müller C; Muntoni F
Neurology; 2005 Dec; 65(12):1930-5. PubMed ID: 16380615
[TBL] [Abstract][Full Text] [Related]
19. Malignant hyperthermia associated with exercise-induced rhabdomyolysis or congenital abnormalities and a novel RYR1 mutation in New Zealand and Australian pedigrees.
Davis M; Brown R; Dickson A; Horton H; James D; Laing N; Marston R; Norgate M; Perlman D; Pollock N; Stowell K
Br J Anaesth; 2002 Apr; 88(4):508-15. PubMed ID: 12066726
[TBL] [Abstract][Full Text] [Related]
20. Oral Dantrolene Reduces Myalgia and Hyperckemia in a Child with RYR1-Related Exertional Myalgia/Rhabdomyolysis.
de Lima Silva EV; Donis KC; Machado FRC; Simão Medeiros L; Aschoff CAM; de Souza CFM; Poswar FO; Saute JAM
J Neuromuscul Dis; 2023; 10(6):1145-1149. PubMed ID: 37781817
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]