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From Symptoms and Signs to Diagnosis in a Rare Disease, Type I Gaucher Disease Cover

From Symptoms and Signs to Diagnosis in a Rare Disease, Type I Gaucher Disease

Internal Medicine
Volume 15 (2018): Issue 1 (March 2018)
By: ,  ,  ,  ,   and    
Open Access
|Mar 2018
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DOI: https://doi.org/10.2478/inmed-2018-0008 | Journal eISSN: 1220-5818 | Journal ISSN: 1220-5818
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Language: English
Page range: 69 - 76
Published on: Mar 24, 2018
Published by: Romanian Society of Internal Medicine
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Keywords:
lysosomal storage disease,
glucocerebrosidase Gaucher's cells,
,
imiglucerase
Related subjects:
Medicine,
Clinical medicine,
Internal medicine,
Internal medicine, other,
Cardiology,
Gastroenterology,
Pneumology

© 2018 Mihaela Ghinea, Sabina Ciocodei, Gabriela Butoi, Geandan Memet, Andreea Stoica, Zizi Niculescu, published by Romanian Society of Internal Medicine
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Volume 15 (2018): Issue 1 (March 2018)
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