Impact of Gaucher disease on COVID ‐19-Reference-Cited by-同舟云学术

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Impact of Gaucher disease on COVID ‐19

Published:2020-07 Issue:7 Volume:50 Page:894-895
ISSN:1444-0903
Container-title:Internal Medicine Journal
language:en
Short-container-title:Intern Med J

Author:

Zimran Ari¹²,Szer Jeff³^ORCID,Revel‐Vilk Shoshana¹²^ORCID

Affiliation:

1. Gaucher UnitShaare Zedek Medical Centre Jerusalem Israel

2. Faculty of MedicineThe Hebrew University of Jerusalem Jerusalem Israel

3. Peter MacCallum Cancer Centre, Royal Melbourne Hospital, and Department of MedicineUniversity of Melbourne Melbourne Victoria Australia

Publisher

Wiley

Subject

Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/imj.14894

Reference5 articles.

1. Complement drives glucosylceramide accumulation and tissue inflammation in Gaucher disease

2. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China

3. ACE phenotyping in Gaucher disease

4. β-Glycosphingolipids as Mediators of Both Inflammation and Immune Tolerance: A Manifestation of Randomness in Biological Systems

Cited by 18 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. Patients with Gaucher disease display systemic elevation of ACE2, which is impacted by therapy status and genotype;Molecular Genetics and Metabolism;2024-09

2. Impact of COVID-19 pandemic on healthcare delivery for lysosomal storage disorders at a tertiary care public hospital in Mumbai;Journal of Postgraduate Medicine;2024-01

3. Management, vaccination status and COVID-19 morbidity of patients with Gaucher disease in Germany during the COVID-19 pandemic;Zeitschrift für Gastroenterologie;2023-01-10

4. Targeting the Complement–Sphingolipid System in COVID-19 and Gaucher Diseases: Evidence for a New Treatment Strategy;International Journal of Molecular Sciences;2022-11-18

5. Lysosomal storage diseases in the era of COVID-19: a report of an Egyptian case of alpha-fucosidosis and a summary of the lysosomal storage diseases-COVID-19 relationship;Egyptian Journal of Medical Human Genetics;2022-09-15

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