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Inborn errors of carbohydrate metabolism / Enzymes / Rare diseases / Glycogen storage disease type II / Alpha-glucosidase / Maltase / Erasmus MC / Medical genetics / Glycogen storage disease / Medicine / Health / Hepatology


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Document Date: 2010-08-10 22:40:31

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File Size: 155,19 KB

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City

Atlanta / Rotterdam / /

Company

MEDLINE / M.L.C. / Elsevier B.V. / Elsevier Inc. / /

Country

United States / Netherlands / /

Facility

Erasmus MC University Medical Center / /

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MedicalCondition

CITATION ALERT Abstracting/Indexing Abstract CITED BY Contact Information Pompe disease / glycogenosis / disorder / acid maltase deficiency / Pompe disease ABSTRACT C.I / deficiency / Pompe disease / /

MedicalTreatment

enzyme replacement therapy / /

Organization

MC University Medical Center / Division of Metabolic Diseases and Genetics / Department of Clinical Genetics / Department of Pediatrics / National Center on Birth Defects and Developmental Disabilities / Department of Pediatric Neurology / Department of Epidemiology & Biostatistics / Centers for Disease Control and Prevention / /

Person

I. van Capellea / Sophia Children / /

/

Position

The Netherlands Corresponding author / GET FULL TEXT ELSEWHERE Author Information Received / /

Technology

PDF / /

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