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

Ghinea, Mihaela; Ciocodei, Sabina; Butoi, Gabriela; Memet, Geandan; Stoica, Andreea; Niculescu, Zizi

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

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Mar 24, 2018

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.

Ghinea, Mihaela

Medical Clinic II, Faculty of Medicine, “Ovidius” UniversityConstanta

Ciocodei, Sabina

Medical Clinic II, County Emergency Clinical Hospital of Constanta

Butoi, Gabriela

Medimar Imagistic Constanta

Memet, Geandan

Medical Clinic II, County Emergency Clinical Hospital of Constanta

Stoica, Andreea

Faculty of Medicine, Ovidius University in Constanta

Niculescu, Zizi

Medical Clinic II, Faculty of Medicine, “Ovidius” UniversityConstanta

Language:: English

Publication timeframe:: 4 times per year
Journal Subjects:: Medicine, Clinical Medicine, Internal Medicine, Internal Medicine, other, Cardiology, Gastroenterology, Pneumology

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

Mihaela Ghinea

Sabina Ciocodei

Gabriela Butoi

Geandan Memet

Andreea Stoica

Zizi Niculescu

Published Online: Mar 24, 2018

Page range: 69 - 76

DOI: https://doi.org/10.2478/inmed-2018-0008

Keywordslysosomal 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.

Keywords
lysosomal storage disease, glucocerebrosidase Gaucher's cells, imiglucerase