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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
Authors

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
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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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