Teaching neuro image: Axial muscle atrophy in adult-onset pompe disease

Neurology

Volumn 70, Issue 10, 2008, Pages e36-

  Katirji, Bashar ^a   Kesner, Vita ^a   Hejal, Rana B ^b   Alshekhlee, Amer ^a   Elkind, Mitchell S V ^a  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE KINASE; GLYCOGEN;

ADULT; ARTICLE; BLOOD; BREATHING MUSCLE; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; DIAPHRAGM PARALYSIS; DIFFERENTIAL DIAGNOSIS; ELECTROMYOGRAPHY; GLYCOGEN STORAGE DISEASE TYPE 2; HUMAN; LYSOSOME; MALE; METABOLISM; MUSCLE ATROPHY; MUSCLE WEAKNESS; PATHOLOGY; PATHOPHYSIOLOGY; RADIOGRAPHY; RESPIRATORY FAILURE; THORAX;

ADULT; CREATINE KINASE; DIAGNOSIS, DIFFERENTIAL; ELECTROMYOGRAPHY; GLYCOGEN; GLYCOGEN STORAGE DISEASE TYPE II; HUMANS; LYSOSOMES; MALE; MUSCLE WEAKNESS; MUSCULAR ATROPHY; RESPIRATORY INSUFFICIENCY; RESPIRATORY MUSCLES; RESPIRATORY PARALYSIS; THORAX; TOMOGRAPHY, X-RAY COMPUTED;

EID: 41649094459     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/01.wnl.0000304251.98684.69     Document Type: Article

References (2)

1. Kishnani PS Corzo D Nicolino M Recombinant human acid alpha-glucosidase: major clinical benefits in infantile-onset Pompe disease Neurology 68 2007 99 107
2. Hagemans ML Hop WJ Van Doorn PA Course of disability and respiratory function in untreated late-onset Pompe disease Neurology 66 2006 581