Long-term bone outcomes in Italian patients with Gaucher disease type 1 or type 3 treated with imiglucerase: A sub-study from the International Collaborative Gaucher Group (ICGG) Gaucher Registry
Author:
Funder
Sanofi
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference18 articles.
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2. The definition of neuronopathic gaucher disease;Schiffmann;J. Inherit. Metab. Dis.,2020
3. Gaucher disease in bone: from pathophysiology to practice;Hughes;J. Bone Miner. Res.,2019
4. A comprehensive study of bone manifestations in adult gaucher disease type 1 patients in Argentina;Oliveri;Calcif. Tissue Int.,2019
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2. Neuronopathic Gaucher disease: Rare in the West, common in the East;Journal of Inherited Metabolic Disease;2024-05-20
3. Endocrinological and metabolic profile of Gaucher disease patients treated with enzyme replacement therapy;Journal of Pediatric Endocrinology and Metabolism;2024-04-17
4. Extensive cardiovascular involvement in a young boy with Gaucher’s disease: a case report;European Heart Journal - Case Reports;2023-09-01
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