Musculoskeletal health in Hunter disease (MPS II): ERT improves functional outcomes

Journal of Pediatric Rehabilitation Medicine

Volumn 3, Issue 2, 2010, Pages 101-107

  White, Klane K ^a   Hale, Susan ^a   Goldberg, Michael J ^a  

^a SEATTLE CHILDREN S HOSPITAL   (United States)

Author keywords

hip; Hunter syndrome; mucopolysaccharidosis; PODCI; spine

Indexed keywords

GLYCOSAMINOGLYCAN; IDURONATE 2 SULFATASE;

ADOLESCENT; ARTICLE; CARPAL TUNNEL SYNDROME; CHILD; CLINICAL ARTICLE; CLINICAL ASSESSMENT; CONTROLLED STUDY; DISEASE SEVERITY; ENZYME REPLACEMENT; FEMALE; FUNCTIONAL ASSESSMENT; HIP MALFORMATION; HUMAN; HUNTER SYNDROME; MALE; MUSCULOSKELETAL DISEASE; MUSCULOSKELETAL FUNCTION; OUTCOME ASSESSMENT; PATIENT MONITORING; PELVIS RADIOGRAPHY; PRESCHOOL CHILD; PRIORITY JOURNAL; PROSPECTIVE STUDY; RANGE OF MOTION; SCHOOL CHILD; SPINE MALFORMATION; SPINE RADIOGRAPHY; TREATMENT DURATION; TREATMENT OUTCOME; VALIDATION STUDY;

EID: 77954629992     PISSN: 18745393     EISSN: 18758894     Source Type: Journal    
DOI: 10.3233/PRM-2010-0112     Document Type: Article

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