Progression from respiratory dysfunction to failure in late-onset Pompe disease

Author:

Berger Kenneth I.,Chan Yinny,Rom William N.,Oppenheimer Beno W.,Goldring Roberta M.

Funder

New York University School of Medicine

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference46 articles.

1. Glycogen storage disease type II: acid alpha-glucosidase (acid maltase) deficiency;Hirschhorn,2001

2. Pompe's disease;van der Ploeg;Lancet,2008

3. Rate of progression and predictive factors for pulmonary outcome in children and adults with Pompe disease;van der Beek;Mol Genet Metab,2011

4. The natural course of non-classic Pompe's disease; a review of 225 published cases;Winkel;J Neurol,2005

5. Late-onset Pompe disease (LOPD): correlations between respiratory muscles CT and MRI features and pulmonary function;Gaeta;Mol Genet Metab,2013

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