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

.blurhash-client-img { display: none !important; }

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

Authors

Mihaela Ghinea

Medical Clinic II, Faculty of Medicine, “Ovidius” University, Constanta

Sabina Ciocodei

Medical Clinic II, County Emergency Clinical Hospital of Constanta

Gabriela Butoi

Medimar Imagistic Constanta

Geandan Memet

Medical Clinic II, County Emergency Clinical Hospital of Constanta

Andreea Stoica

Faculty of Medicine, Ovidius University in Constanta

Zizi Niculescu

Medical Clinic II, Faculty of Medicine, “Ovidius” University, Constanta

DOI: https://doi.org/10.2478/inmed-2018-0008 | Journal eISSN: 1220-5818 | Journal ISSN: 1220-5818

Journal RSS Feed

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.

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