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Journals
Internal Medicine
Volume 15 (2018): Issue 1 (March 2018)
Open Access
From Symptoms and Signs to Diagnosis in a Rare Disease, Type I Gaucher Disease
Mihaela Ghinea
Mihaela Ghinea
,
Sabina Ciocodei
Sabina Ciocodei
,
Gabriela Butoi
Gabriela Butoi
,
Geandan Memet
Geandan Memet
,
Andreea Stoica
Andreea Stoica
and
Zizi Niculescu
Zizi Niculescu
| Mar 24, 2018
Internal Medicine
Volume 15 (2018): Issue 1 (March 2018)
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Published Online:
Mar 24, 2018
Page range:
69 - 76
DOI:
https://doi.org/10.2478/inmed-2018-0008
Keywords
lysosomal storage disease
,
glucocerebrosidase Gaucher's cells
,
imiglucerase
© 2018 Mihaela Ghinea et al., published by De Gruyter Open
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
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