Infantile‐onset Pompe disease with neutropenia: Treatment decisions in the face of a unique phenotype-Reference-Cited by-同舟云学术

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Infantile‐onset Pompe disease with neutropenia: Treatment decisions in the face of a unique phenotype

Published:2022-09-27 Issue:1 Volume:64 Page:17-22
ISSN:2192-8312
Container-title:JIMD Reports
language:en
Short-container-title:JIMD Reports

Author:

Riedy Mary¹^ORCID,Zhang Jeff F.²,Huang Taosheng³,Swayampakula Anil Kumar⁴

Affiliation:

1. Department of Pharmacy Practice, School of Pharmacy and Pharmaceutical Sciences University at Buffalo Buffalo New York USA

2. Jacobs School of Medicine and Biomedical Sciences University at Buffalo Buffalo New York USA

3. Division of Genetics, Department of Pediatrics University at Buffalo Buffalo New York USA

4. Division of Critical Care Medicine, Department of Pediatrics, John R. Oishei Children's Hospital University at Buffalo Buffalo New York USA

Publisher

Wiley

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12337

Reference30 articles.

1. Pompe Disease

2. Infantile onset Pompe disease: A report of physician narratives from an epidemiologic study

3. Cardiac responses in paediatric Pompe disease in the ADVANCE patient cohort

4. Recombinant human acid -glucosidase: Major clinical benefits in infantile-onset Pompe disease

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