The importance of nutritional status in the prognosis of late onset Pompe disease

Molecular Genetics and Metabolism

Volumn 100, Issue 4, 2010, Pages 389-

  Papadimas, G K ^a   Terzis, G ^a,b   Papadopoulos, C ^a   Spengos, K ^a   Manta, P ^a  

^a UNIVERSITY OF ATHENS MEDICAL SCHOOL   (Greece)

^b UNIVERSITY OF ATHENS   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLUCOSIDASE;

BODY MASS; CORRELATIONAL STUDY; DISEASE SEVERITY; ENZYME ACTIVITY; ENZYME REPLACEMENT; FIBROBLAST; GLYCOGEN STORAGE DISEASE TYPE 2; HUMAN; LETTER; NUTRITIONAL STATUS; OUTCOME ASSESSMENT; PRIORITY JOURNAL; PROGNOSIS; SKIN CULTURE; TREATMENT DURATION; TREATMENT RESPONSE; ADULT; ENZYMOLOGY; GLYCOGEN STORAGE DISEASE TYPE II; ONSET AGE; PATHOLOGY;

ADULT; AGE OF ONSET; ALPHA-GLUCOSIDASES; BODY MASS INDEX; ENZYME REPLACEMENT THERAPY; FIBROBLASTS; GLYCOGEN STORAGE DISEASE TYPE II; HUMANS; NUTRITIONAL STATUS; PROGNOSIS;

EID: 77954659727     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2010.04.012     Document Type: Letter

References (4)

1. Kobayashi H., Shimada Y., Ikegami M., Kawai T., Sakurai K., Urashima T., Ijima M., Fujiwara M., Kaneshiro E., Ohashi T., Eto Y., Ishigaki K., Osawa M., Kyosen S.O., Ida H. Prognostic factors for the late onset Pompe disease with enzyme replacement therapy: From our experience of four cases including an autopsy case. Mol. Genet. Metab. 2010, 100:14-19.
2. S. Ravaglia, C. Danesino, A. Moglia, A. Costa, L. Maccarini, A. Carlucci, A. Pichiecchio, P. Bini, P. De Filippi, M. Rossi, Changes in nutritional status and body composition during enzyme replacement therapy in adult-onset type II glycogenosis, Eur. J. Neurol., 2010, [Ahead of print].
3. Ravaglia S., Danesino C., Pichiecchio A., Repetto A., Poloni G.U., Rossi M., Fratino P., Moglia A., Costa A. Enzyme replacement therapy in severe adult-onset glucogen storage disease type II. Adv. Ther. 2008, 25:820-829.
4. Beratis N.G., LaBadie G.U., Hirschhorn R. Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts. J. Clin. Invest. 1978, 62:1264-1274.