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The emerging phenotype of long-term survivors with infantile Pompe disease

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Year: 2012
Type: article
Study design: Observational Study
Source: Genetics in Medicine
DOI: 10.1038/gim.2012.44
Authors: Sean N. Prater, Suhrad G. Banugaria, Stephanie M. DeArmey, Eleanor G. Botha, Erin M. Stege, Laura E. Case, Harrison N. Jones, Chanika Phornphutkul, Raymond Y. Wang, Sarah P. Young, Priya S. Kishnani
Institutions: Duke Medical Center, Emory University, Duke University, Brown University, Rhode Island Hospital, Children's Hospital of Orange County, University of California, Irvine
Language: English

Topic: Lysosomal Storage Disorders Research
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: bronze

Funders: Rare Diseases Clinical Research Network, National Institutes of Health, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke, National Center for Research Resources
Awards: COBRE for Skeletal Health and Repair, Duke CTSI, Lysosomal Disease Network, Duke CTSI
OpenAlex ID: W2041769721
FWCI: 8.722
Cites: 37
Cited by: 198
Related to: 10
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