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S1.3 Adult-onset Pompe disease

By Giuseppe Di Iorio, Federica Cipullo, Lucia Stromillo, Luisa Sodano, Elisa Capone and Olimpia Farina
Topics: Session 1. Pompe Disease: Clinical, Diagnostic and Genetic Aspects
Publisher: Pacini Editore SpA
OAI identifier: oai:pubmedcentral.nih.gov:3298100
Provided by: PubMed Central
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    1. American Association of Neuromuscular & Electrodiagnostic Medicine Diagnostic criteria for late-onset (childhood and adult) Pompe disease.
    2. Late onset Pompe disease: clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients.
    3. Lysosomal storage disease 2. Pompe disease.
    4. Pompe disease (glycogen storage disease type II): clinical features and enzyme replacement therapy.

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