LATE COMPONENTS OF MOTOR UNIT POTENTIALS IN CENTRAL CORE DISEASELOPEZ TERRADAS JM; CONDE LOPEZ M.1979; J. NEUROL. NEUROSURG. PSYCHIATRY; GBR; DA. 1979; VOL. 42; NO 5; PP. 461-464; BIBL. 20 REF.Article

ENZYME REACTIONS IN BEIGE MOUSE MUSCLE WITH CENTRAL CORESKIRKEBY S.1981; ACTA NEUROPATHOL.; ISSN 0001-6322; DEU; DA. 1981; VOL. 54; NO 4; PP. 325-327; BIBL. 14 REF.Article

CENTRAL CORE DISEASE: HISTOCHEMICAL AND ULTRASTRUCTURAL STUDY OF MUSCLE BIOPSIES OF FATHER AND DAUGHTER.PALMUCCI L; SCHIFFER D; MONGA G et al.1978; J. NEUROL.; GERM.; DA. 1978; VOL. 218; NO 1; PP. 55-62; BIBL. 1 P. 1/2Article

BEITRAG ZUR CENTRAL CORE DISEASE. I. LICHTMIKROSKOPISCHE UND HISTOCHEMISCHE UNTERSUCHUNGEN. = MYOPATHIE CENTRAL CORE. I. ETUDES HISTOCHIMIQUES ET AU MICROSCOPE OPTIQUEMEEBACH W; GRAEBNER R.1977; ZBL. ALLG. PATHOL. PATHOL. ANAT.; DTSCH.; DA. 1977; VOL. 121; NO 1-2; PP. 169-176; ABS. ANGL.; BIBL. 1 P. 1/2Article

LA MYOPATHIE A AXE CENTRAL: ETUDE OPTIQUE, HISTOENZYMOLOGIQUE ET ULTRASTRUCTURALE DE 2 CAS AVEC REVUE DE LA LITTERATUREPAGES A; PAGES M.1981; ANN. PATHOL.; FRA; DA. 1981; VOL. 1; NO 1; PP. 38-47; ABS. ENG; BIBL. 2 P.Article

BEITRAG ZUR CENTRAL CORE DISEASE. II. ELEKTRONENOPTISCHE UNTERSUCHUNGEN. = MYOPATHIE CENTRAL CORE. II. ETUDE AU MICROSCOPE ELECTRONIQUEMEERBACH W; LAGEMAN A; DIETZ W et al.1977; ZBL. ALLG. PATHOL. PATHOL. ANAT.; DTSCH.; DA. 1977; VOL. 121; NO 1-2; PP. 177-185; ABS. ANGL.; BIBL. 20 REF.Article

CENTRAL CORE DISEASE KLINISCHE UND PATHOLOGISCH-ANATOMISCHE BEFUNDE EINES FALLES. = CENTRAL CORE DISEASE. SIGNES CLINIQUES ET ANATOMOPATHOLOGIQUES DANS UN CASHOCHHEIM B; MEERBACH W.1977; BEITR. ORTHOP. TRAUMATOL.; DTSCH.; DA. 1977; VOL. 24; NO 11; PP. 618-624; BIBL. 17 REF.Article

CENTRAL CORE DISEASE AND MALIGNANT HYPERTHERMIA SYNDROMEFRANK JP; HARATI Y; BUTLER IJ et al.1980; ANN. NEUROL.; USA; DA. 1980; VOL. 7; NO 1; PP. 11-17; BIBL. 38 REF.Article

CENTRAL CORE DISEASE: CLINICAL AND PATHOLOGICAL EVIDENCE OF PROGRESSION WITHIN A FAMILYPATTERSON VH; HILL TRG; FLETCHER PJH et al.1979; BRAIN; GBR; DA. 1979; VOL. 102; NO 3; PP. 581-594; BIBL. 16 REF.Article

SINGLE FIBRE ELECTROMYOGRAPHY IN CENTRAL CORE DISEASECRUZ MARTINEZ A; FERRER MT; LOPEZ TERRADAS JM et al.1979; J. NEUROL. NEUROSURG. PSYCHIATRY; GBR; DA. 1979; VOL. 42; NO 7; PP. 662-667; BIBL. 2 REF.Article

MALIGNANT HYPERTHERMIA AND CENTRAL CORE DISEASE IN A CHILD WITH CONGENITAL DISLOCATING HIPS. CASE PRESENTATION AND REVIEW.ENG GD; EPSTEIN BS; ENGEL WK et al.1978; ARCH. NEUROL.; U.S.A.; DA. 1978; VOL. 35; NO 4; PP. 189-197; BIBL. 2 P.Article

FOCAL ABNORMALITIES IN MITOCHONDRIAL DISTRIBUTION IN MUSCLE. TWO ATYPICAL CASES OF SO-CALLED "CENTRAL CORE DISEASE".RADU H; ROSU SERBU AM; IONESCU V et al.1977; ACTA NEUROPATHOL.; ALLEM.; DA. 1977; VOL. 39; NO 1; PP. 25-31; BIBL. 33 REF.Article

Une posture atypique chez le sujet âgé : la camptocormie = Atypical attitude in old age: camptocormiaLLESHI, Enver; MORISOD, Jérome; COUTAZ, Martial et al.La Revue de gériatrie. 2002, Vol 27, Num 9, pp 764-765, issn 0397-7927, 2 p.Article

Caesarean section in a complicated case of central core diseaseFOSTER, R. N; BOOTHROYD, K. P.Anaesthesia. 2008, Vol 63, Num 5, pp 544-547, issn 0003-2409, 4 p.Article

MUSCLE FRUCTOSE 1,6-DIPHOSPHATASE DEFICIENCY ASSOCIATED WITH AN ATYPICAL CENTRAL CORE DISEASEKAR NC; PEARSON CM; VERITY MA et al.1980; J. NEUROL. SCI.; ISSN 0022-510X; NLD; DA. 1980; VOL. 48; NO 2; PP. 243-256; BIBL. 2 P.Article

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

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

A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 geneFERREIRO, Ana; MONNIER, Nicole; LEMAINQUE, Arnaud et al.Annals of neurology. 2002, Vol 51, Num 6, pp 750-759, issn 0364-5134Article

Central core disease and congenital neuromuscular disease with uniform type 1 fibers in one familyTOJO, M; OZAWA, M; NONAKA, I et al.Brain & development (Tokyo. 1979). 2000, Vol 22, Num 4, pp 262-264, issn 0387-7604Article

Expression of cytoskeleton proteins in central core diseaseVITA, G; MIGLIORATO, A; BARADELLO, A et al.Journal of the neurological sciences. 1994, Vol 124, Num 1, pp 71-76, issn 0022-510XArticle

Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19KAUSCH, K; LEHMANN-HORN, F; JANKA, M et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 3, pp 765-769, issn 0888-7543, 5 p.Article

Muscle weakness in a 16-year-old girlMACAULAY, R. J. B; SLADKY, J. T; JAY, V et al.Pediatric neurosurgery. 1993, Vol 19, Num 2, pp 93-100, issn 1016-2291Article

Orthopaedic aspects of central core diseaseGAMBLE, J. G; RINSKY, L. A; LEE, J. H et al.Journal of bone and joint surgery. American volume. 1988, Vol 70A, Num 7, pp 1061-1066, issn 0021-9355Article

Is central core disease with structural core a fetal defect?FIDZIANSKA, A; NIEBROJ-DOBOSZ, I; BADURSKA, B et al.Journal of neurology. 1984, Vol 231, Num 4, pp 212-219, issn 0340-5354Article