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

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

Internal Medicine

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

By: Mihaela Ghinea, Sabina Ciocodei, Gabriela Butoi, Geandan Memet, Andreea Stoica and Zizi Niculescu

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,

,

Related subjects:

Clinical medicine,

Internal medicine,

Internal medicine, other,

Gastroenterology,

© 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.

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