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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
Medical Clinic II, Faculty of Medicine, “Ovidius” University
Constanta,
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Ghinea, Mihaela
,
Sabina Ciocodei
Sabina Ciocodei
Medical Clinic II, County Emergency Clinical Hospital of Constanta
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Ciocodei, Sabina
,
Gabriela Butoi
Gabriela Butoi
Medimar Imagistic Constanta
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Butoi, Gabriela
,
Geandan Memet
Geandan Memet
Medical Clinic II, County Emergency Clinical Hospital of Constanta
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Memet, Geandan
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Andreea Stoica
Andreea Stoica
Faculty of Medicine, Ovidius University in Constanta
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Stoica, Andreea
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Zizi Niculescu
Zizi Niculescu
Medical Clinic II, Faculty of Medicine, “Ovidius” University
Constanta,
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Niculescu, Zizi
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.
