Neuroimaging findings in infantile Pompe patients treated with enzyme replacement therapy-Reference-Cited by-同舟云学术

Neuroimaging findings in infantile Pompe patients treated with enzyme replacement therapy

Published:2018-02 Issue:2 Volume:123 Page:85-91
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

McIntosh Paul T.,Hobson-Webb Lisa D.,Kazi Zoheb B.,Prater Sean N.,Banugaria Suhrad G.,Austin Stephanie,Wang Raymond,Enterline David S.,Frush Donald P.,Kishnani Priya S.

Funder

Genzyme Corporation

Lysosomal Disease Network

NIH Rare Diseases Clinical Research Network

NCATS

National Institute of Neurological Disorders and Stroke

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference33 articles.

1. A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease;Kishnani;J. Pediatr.,2006

2. Infantile onset Pompe disease: a report of physician narratives from an epidemiologic study;Marsden;Genet. Med.,2005

3. The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature;van den Hout;Pediatrics,2003

4. Glycogen storage disease type II: Acid a-glucosidase (acid maltase) deficiency;Hirschhorn,2010

5. Nervous system in Pompe's disease. Ultrastructure and biochemistry;Gambetti;J. Neuropathol. Exp. Neurol.,1971

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