Rhabdomyolysis in pontocerebellar hypoplasia type 2 (PCH-2)

Neuromuscular Disorders

Volumn 18, Issue 1, 2008, Pages 52-58

  Barth, Peter G ^a   Ryan, Monique M ^b,c   Webster, Richard I ^d,e   Aronica, Eleonora ^a   Kan, Alex ^d   Ramkema, Marja ^a   Jardine, Philip ^f   Poll The, Bwee Tien ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

^b ROYAL CHILDREN'S HOSPITAL   (Australia)

^c MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

^d CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^e UNIVERSITY OF SYDNEY   (Australia)

^f BRISTOL ROYAL HOSPITAL FOR CHILDREN   (United Kingdom)

Author keywords

Olivopontocerebellar hypoplasia; Pontocerebellar hypoplasia type 2; Rhabdomyolysis

Indexed keywords

CREATINE KINASE; HLA ANTIGEN;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CLINICAL ARTICLE; DEGENERATIVE DISEASE; FEMALE; HUMAN; HUMAN TISSUE; INFANT; MALE; MUSCLE BIOPSY; MYOPATHY; NEUROMUSCULAR DISEASE; PONTOCEREBELLAR HYPOPLASIA TYPE 2; PRESCHOOL CHILD; PRIORITY JOURNAL; RHABDOMYOLYSIS; UPREGULATION;

ADULT; CEREBELLUM; CHILD, PRESCHOOL; CHROMOSOME DISORDERS; CREATINE KINASE; FEMALE; GENES, RECESSIVE; HLA ANTIGENS; HUMANS; INFANT; INFANT, NEWBORN; MALE; MICROSCOPY, ELECTRON, TRANSMISSION; MUSCLE FIBERS; MUSCLE, SKELETAL; NECROSIS; OLIVOPONTOCEREBELLAR ATROPHIES; PONS; RHABDOMYOLYSIS;

EID: 38749115861     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2007.08.001     Document Type: Article

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