Tratamiento en la enfermedad de Fabry-Reference-Cited by-同舟云学术

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Tratamiento en la enfermedad de Fabry

Published:2018-12 Issue:9 Volume:218 Page:489-495
ISSN:0014-2565
Container-title:Revista Clínica Española
language:es
Short-container-title:Revista Clínica Española

Author:

López Rodríguez M.

Publisher

Elsevier BV

Subject

General Medicine

Reference39 articles.

1. Enzymatic abnormalities in diseases of sphingolipid metabolism;Brady;Clin Chem.,1967

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

3. The frequency of lysosomal storage diseases in The Netherlands;Poorthuis;Hum Genet.,1999

4. Case-finding in Fabry disease: experience from the North of England;Brennan;J Inherit Metab Dis.,2014

5. Uncertain diagnosis of Fabry disease in patients with neuropathic pain. Angiokeratoma or cornea verticillata: Consensus on the approach to diagnosis and follow-up;Van der Tol;JIMD Rep.,2014

Cited by 3 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. Expert opinion on the recognition, diagnosis and management of children and adults with Fabry disease: a multidisciplinary Turkey perspective;Orphanet Journal of Rare Diseases;2022-03-02

2. New molecular entities and structure–activity relationships of drugs designed by the natural product derivatization method from 2010 to 2018;Bioactive Natural Products;2021

3. Biovalorization of cheese whey and molasses wastes to galactosidases by recombinant yeasts;Biovalorisation of Wastes to Renewable Chemicals and Biofuels;2020

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