Bone manifestations in neuronopathic Gaucher disease while receiving high-dose enzyme replacement therapy-Reference-Cited by-同舟云学术

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Bone manifestations in neuronopathic Gaucher disease while receiving high-dose enzyme replacement therapy

Published:2019-02 Issue:2 Volume:126 Page:157-161
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Potnis Kunal C.,Flueckinger Lauren B.,Ha Christine I.,Upadia Jariya,Frush Donald P.,Kishnani Priya S.

Publisher

Elsevier BV

Subject

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

Reference31 articles.

1. Acid beta-glucosidase: enzymology and molecular biology of Gaucher disease;Grabowski;Crit. Rev. Biochem. Mol. Biol.,1990

2. Skeletal aspects of Gaucher disease: a review;Wenstrup;Br. J. Radiol.,2002

3. Eight-year clinical outcomes of long-term enzyme replacement therapy for 884 children with Gaucher disease type 1;Andersson;Pediatrics,2008

4. Combination therapy in a patient with chronic neuronopathic Gaucher disease: a case report;Ceravolo;J. Med. Case Rep.,2017

5. Phenotypic continuum in neuronopathic Gaucher disease: an intermediate phenotype between type 2 and type 3;Goker-Alpan;J. Pediatr.,2003

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1. Neuronopathic Gaucher disease: Rare in the West, common in the East;Journal of Inherited Metabolic Disease;2024-05-20

2. Changing clinical manifestations of Gaucher disease in Taiwan;Orphanet Journal of Rare Diseases;2023-09-15

3. Osteonecrosis in Gaucher disease in the era of multiple therapies: Biomarker set for risk stratification from a tertiary referral center;eLife;2023-05-30

4. Osteonecrosis in Gaucher Disease in the era of multiple therapies: biomarker set for risk stratification from a tertiary referral center;2023-03-27

5. Gaucher disease – more than just a rare lipid storage disease;Journal of Molecular Medicine;2022-01-23

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