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kw.\*:("central core disease")

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Central core disease is due to RYRI mutations in more than 90% of patientsSHIWEN WU; IBARRA M, Carlos A; MALICDAN, May Christine V et al.Brain. 2006, Vol 129, pp 1470-1480, issn 0006-8950, 11 p., 6Article

Central core disease due to recessive mutations in RYR1 gene : Is it more common than described?KOSSUGUE, Patricia M; PAIM, Julia F; NAVARRO, Monica M et al.Muscle & nerve. 2007, Vol 35, Num 5, pp 670-674, issn 0148-639X, 5 p.Article

Malignant hyperthermia and central core disease causative mutations in Swedish patientsBROMAN, M; ISLANDER, G; MULLER, C. R et al.Acta anaesthesiologica scandinavica. 2007, Vol 51, Num 1, pp 50-53, issn 0001-5172, 4 p.Article

Sarcoplasmic reticulum : The dynamic calcium governor of muscleROSSI, Ann E; DIRKSEN, Robert T.Muscle & nerve. 2006, Vol 33, Num 6, pp 715-731, issn 0148-639X, 17 p.Article

Pilot trial of salbutamol in central core and multi-minicore diseasesMESSINA, S; HARTLEY, L; MAIN, M et al.Neuropediatrics. 2004, Vol 35, Num 5, pp 262-266, issn 0174-304X, 5 p.Article

Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscleBÖNNEMANN, C. G; THOMPSON, T. G; BEGGS, A. H et al.Journal of the neurological sciences. 2003, Vol 206, Num 1, pp 71-78, issn 0022-510X, 8 p.Article

Central core diseaseGULATI, Sheffali; SALHOTRA, Amandeep; SHARMA, M. C et al.Indian journal of pediatrics. 2004, Vol 71, Num 11, pp 1021-1024, issn 0019-5456, 4 p.Article

Molecular mechanisms and phenotypic variation in RYRI-related congenital myopathiesHAIYAN ZHOU; JUNGBLUTH, Heinz; KINALI, Maria et al.Brain. 2007, Vol 130, pp 2024-2036, issn 0006-8950, 13 p., 8Article

Joint hypermobility as a distinctive feature in the differential diagnosis of myopathiesVOERMANS, N. C; BONNEMANN, C. G; HAMEL, B. C. J et al.Journal of neurology. 2009, Vol 256, Num 1, pp 13-27, issn 0340-5354, 15 p.Article

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