Immunoglobulin Abnormalities in Gaucher Disease: an Analysis of 278 Patients Included in the French Gaucher Disease Registry

Autor: Yann Nguyen, Dries Dobbelaere, Jérôme Stirnemann, Monia Bengherbia, Fabrice Camou, Samia Pichard, Karima Yousfi, Christine Serratrice, Agathe Masseau, Vanessa Leguy-Seguin, Marc G. Berger, Nadia Belmatoug, Dalil Hamroun, Bruno Fantin, Florent Lautredoux, Francis Gaches, Leonardo Astudillo, Anaïs Brassier, Bérengère Cador, Florence Dalbies, Yves-Marie Pers, Thierry Billette de Villemeur

Publikováno v: International Journal of Molecular Sciences
Volume 21
Issue 4
International Journal of Molecular Sciences, 2020, 21 (4), pp.1247. ⟨10.3390/ijms21041247⟩
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1247 (2020)
International Journal of Molecular Sciences, Vol. 21, No 4 (2020) P. 1247
International Journal of Molecular Sciences, MDPI, 2020, 21 (4), pp.1247. ⟨10.3390/ijms21041247⟩

Gaucher disease (GD) is a rare lysosomal autosomal-recessive disorder due to deficiency of glucocerebrosidase
polyclonal gammopathy (PG) and/or monoclonal gammopathy (MG) can occur in this disease. We aimed to describe these immunoglobulin abnor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90aee55c5e8ec2af6466291e46dc07c6

A Cross-Sectional Retrospective Study of Non-Splenectomized and Never-Treated Patients with Type 1 Gaucher Disease

Autor: Isabelle Durieu, Leonardo Astudillo, Ivan Bertchansky, Samia Pichard, Amina Berrahal, Nadia Belmatoug, Roseline Froissart, Catherine Caillaud, Monia Bengherbia, Jérôme Stirnemann, Vanessa Leguy Seguin, Karima Yousfi, Bérengère Cador, Marc G. Berger, Laure Swiader, Catherine Marcel, Claire de Moreuil, Bénédicte Hivert, Sébastien Humbert, Thierry Billette de Villemeur, Christine Serratrice, Brigitte Chabrol, Isabelle Hau Rainsard, Agathe Masseau, Fabrice Camou, Anaïs Brassier, Florence Dalbies

Publikováno v: Journal of Clinical Medicine, Vol. 9, No 8 (2020) P. 2343
Journal of Clinical Medicine
Journal of Clinical Medicine; Volume 9; Issue 8; Pages: 2343
Journal of Clinical Medicine, 2020, 9 (8), pp.2343. ⟨10.3390/jcm9082343⟩
Journal of Clinical Medicine, MDPI, 2020, 9 (8), pp.2343. ⟨10.3390/jcm9082343⟩
Journal of Clinical Medicine, Vol 9, Iss 2343, p 2343 (2020)

International audience; Patients with type 1 Gaucher disease (GD1) present thrombocytopenia, anemia, organomegaly, and bone complications. Most experts consider that the less aggressive forms do not require specific treatment. However, little is know

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25191cbc046a11eeca95291a613c0f1e
https://archive-ouverte.unige.ch/unige:145459

The intra-monocyte pharmacokinetics of imiglucerase suggests a possible personalization of enzyme replacement therapy in patients with GD1

Autor: Marc G. Berger, Juliette Berger, Marie Vigan, Bruno Pereira, Roseline Froissart, Nadia Belmatoug, Florence Dalbies, Agathe Masseau, Christian Rose, Christine Serratrice, Yves-Maris Pers, Ivan Bertschanski, Monia Bengherbia, Céline Bourgne, Alexandre Janel, Catherine Caillaud, Magali Pettazzoni, Amina Berrahal, Jérôme Stirnemann, France Mentré

Publikováno v: Molecular Genetics and Metabolism. 123:S23-S24

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1d08cd36e6d419cb019aa6e784f7966d
https://doi.org/10.1016/j.ymgme.2017.12.035

Gaucher disease: French registry cohort of 58 patients treated with eliglustat

Autor: Marc G. Berger, Monia Bengherbia, Fabrice Camou, Jérôme Stirnemann, Céline Verstuyft, Nadia Belmatoug

Publikováno v: Molecular Genetics and Metabolism. 123:S28

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::45b1d95d81eaf8a68ab7c218515fd61b
https://doi.org/10.1016/j.ymgme.2017.12.049

Effects of switching from imiglucerase to velaglucerase alfa without dose reduction nor wash out in type 1 Gaucher disease

Autor: Monia Bengherbia, Nadia Belmatoug, Marc G. Berger, Bernard Grosbois, Marine Alessandrini, Comité d'Evaluation et de Traitement de la maladie de Gaucher, Yves-Marie Pers, Fabrice Camou, Michael Bismuth, Christine Serratrice, Isabelle Marie

Publikováno v: Blood cells, moleculesdiseases. 53(1-2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa7d85f871b83e842632ffdad5005433
https://pubmed.ncbi.nlm.nih.gov/24411065