Similarities and differences between Gaucher disease and acid sphingomyelinase deficiency: An algorithm to support the diagnosis-Reference-Cited by-同舟云学术

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Similarities and differences between Gaucher disease and acid sphingomyelinase deficiency: An algorithm to support the diagnosis

Published:2023-02 Issue: Volume:108 Page:81-84
ISSN:0953-6205
Container-title:European Journal of Internal Medicine
language:en
Short-container-title:European Journal of Internal Medicine

Author:

Cappellini Maria Domenica,Motta Irene,Barbato Antonio^ORCID,Giuffrida Gaetano,Manna Raffaele,Carubbi Francesca,Giona Fiorina

Publisher

Elsevier BV

Subject

Internal Medicine

Reference25 articles.

1. Lysosomal storage diseases: from pathophysiology to therapy;Parenti;Annu Rev Med,2015

2. Phenotype, diagnosis, and treatment of Gaucher's disease;Grabowski;Lancet,2008

3. GBA, Gaucher Disease, and Parkinson’s Disease: from genetic to clinic to new therapeutic approaches;Riboldi;Cells,2019

4. Gaucher disease types 1 and 3: phenotypic characterization of large populations from the ICGG Gaucher Registry;Grabowski;Am J Hematol,2015

5. Prevalence of lysosomal storage disorders;Meikle;JAMA,1999

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Imiglucerase, cholecalciferol, and bone-diet in skeletal health management of type I Gaucher disease patients: a pilot study and systematic review;JBMR Plus;2024-05-27

2. Gaucher Disease or Acid Sphingomyelinase Deficiency? The Importance of Differential Diagnosis;Journal of Clinical Medicine;2024-03-05

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