Pulmonary involvement in selected lysosomal storage diseases and the impact of enzyme replacement therapy: A state‐of‐the art review
Author:
Affiliation:
1. Department of Genetics and Clinical Immunology National Institute of Tuberculosis and Lung Diseases Warsaw Poland
2. Department of Pediatrics, Nutrition and Metabolic Diseases The Children's Memorial Health Institute Warsaw Poland
Publisher
Wiley
Subject
Genetics(clinical),Pulmonary and Respiratory Medicine,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/crj.13150
Reference35 articles.
1. Enzyme Replacement Therapy: A Review and Its Role in Treating Lysosomal Storage Diseases
2. CNS, lung, and lymph node involvement in Gaucher disease type 3 after 11years of therapy: Clinical, histopathologic, and biochemical findings
3. Gaucher Cells in Pulmonary-Capillary Blood in Association with Pulmonary Hypertension
4. Hepatopulmonary Syndrome in Gaucher Disease With Right-to-Left Shunt
5. Lung Transplantation in Gaucher Disease
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