Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Djazia Heraoui"'
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Akademický článek
A prospective study of bone marrow hematopoietic and mesenchymal stem cells in type 1 Gaucher disease patients.
Autor: Séverine Lecourt, Enguerran Mouly, Delphine Freida, Audrey Cras, Raphaël Ceccaldi, Djazia Heraoui, Christine Chomienne, Jean-Pierre Marolleau, Bertrand Arnulf, Raphael Porcher, Catherine Caillaud, Valérie Vanneaux, Nadia Belmatoug, Jérôme Larghero
Publikováno v: PLoS ONE, Vol 8, Iss 7, p e69293 (2013)
Gaucher disease (GD) is an autosomal recessive disorder characterized by lysosomal glucocerebrosidase (GBA) deficiency leading to hematological and skeletal manifestations. Mechanisms underlying these symptoms have not yet been elucidated. In vivo, b
Externí odkaz: https://doaj.org/article/f4bc4093050b4776bb8251cfba5bb914
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2
Ferritinemia during type 1 Gaucher disease: Mechanisms and progression under treatment
Autor: Jérôme Stirnemann, Christian Rose, Nadia Belmatoug, Olivier Fain, Djazia Heraoui, Bruno Fantin, Arsène Mekinian, Agnès Charpentier
Publikováno v: Blood Cells, Molecules, and Diseases. 49:53-57
Background Earlier results highlighted hyperferritinemia during type-1 Gaucher disease (GD), but its potential mechanisms and long-term progression remained unexamined. Methods We analyzed the clinical, biological and iron characteristics of type-1 G
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50330a73a49b43ddcfd5e3c2053a9782
https://doi.org/10.1016/j.bcmd.2012.04.002
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3
Bone Marrow Microenvironment in an In Vitro Model of Gaucher Disease: Consequences of Glucocerebrosidase Deficiency
Autor: Nadia Belmatoug, Linda Herbi, Christine Chomienne, Jean-Pierre Marolleau, Audrey Cras, Valérie Vanneaux, Djazia Heraoui, Jérôme Larghero, Delphine Freida, Catherine Caillaud, Séverine Lecourt
Publikováno v: Stem Cells and Development. 21:239-248
Gaucher disease (GD) is a lysosomal storage disorder due to glucocerebrosidase (GBA) deficiency. Mechanisms leading to the emergence of hematological and skeletal manifestations observed in GD are poorly explained. Bone marrow (BM) mesenchymal stem c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::969157ee26cdbc4c4acc0948263302d2
https://doi.org/10.1089/scd.2011.0365
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5
A prospective study of bone marrow hematopoietic and mesenchymal stem cells in type 1 Gaucher disease patients
Autor: Djazia Heraoui, Christine Chomienne, Audrey Cras, Nadia Belmatoug, Valérie Vanneaux, Catherine Caillaud, Enguerran Mouly, Séverine Lecourt, Raphael Ceccaldi, Bertrand Arnulf, Jean-Pierre Marolleau, Raphaël Porcher, Jérôme Larghero, Delphine Freida
Publikováno v: PLoS ONE, Vol 8, Iss 7, p e69293 (2013)
PLoS ONE
Gaucher disease (GD) is an autosomal recessive disorder characterized by lysosomal glucocerebrosidase (GBA) deficiency leading to hematological and skeletal manifestations. Mechanisms underlying these symptoms have not yet been elucidated. In vivo, b
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb5ed22dfbb646666682cf6d125d50ce
http://europepmc.org/articles/PMC3723887?pdf=render
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6
The French Gaucher's disease registry: clinical characteristics, complications and treatment of 562 patients
Autor: Christine de Roux-Serratrice, Jérôme Stirnemann, Dries Dobbelaere, Bernard Grosbois, Olivier Fain, Fabrice Camou, Thierry Levade, Agathe Masseau, Vassili Valayanopoulos, Djazia Heraoui, Marc G. Berger, Bruno Fantin, Marie T. Vanier, Cyril Mignot, Linda Rossi-Semerano, Catherine Caillaud, Christian Rose, Nadia Belmatoug, Alain Robert, Frédéric Sedel, Marie Vigan, P. Kaminsky, Thierry Billette de Villemeur, Dalil Hamroun, Roselyne Froissart
Publikováno v: Orphanet Journal of Rare Diseases, Vol. 7 (2012) P. 77
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2012, 7 (1), pp.77. ⟨10.1186/1750-1172-7-77⟩
Orphanet Journal of Rare Diseases, 2012, 7 (1), pp.77. ⟨10.1186/1750-1172-7-77⟩
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 77 (2012)
Orphanet Journal of Rare Diseases, BioMed Central, 2012, 7 (1), pp.77. 〈10.1186/1750-1172-7-77〉
Background Clinical features, complications and treatments of Gaucher’s disease (GD), a rare autosomal–recessive disorder due to a confirmed lysosomal enzyme (glucocerebrosidase) deficiency, are described. Methods All patients with known GD, livi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c631ddefd5e55795095ec12e5238f0b7
https://archive-ouverte.unige.ch/unige:78658
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8
Impact of imiglucerase on the serum glycosylated-ferritin level in Gaucher disease
Autor: Olivier Fain, Nadia Belmatoug, Djazia Heraoui, Jérôme Stirnemann, Arsène Mekinian, Anne Boutten, Corine Vincent, Bruno Fantin
Publikováno v: Blood cells, moleculesdiseases. 46(1)
Gaucher disease (GD) is a lysosomal storage disorder, caused by deficient activity of the enzyme glucocerebrosidase, which can be treated by enzyme-replacement therapy (ERT). No prognostic marker can predict long-term complications of GD but several
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcdc081a780e495e9fca1380fb6a63ee
https://pubmed.ncbi.nlm.nih.gov/21084203
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10
Maladie de Gaucher et grossesse
Autor: Nadia Belmatoug, Djazia Heraoui
Publikováno v: La Presse Médicale. 38:2S17-2S23
La maladie de Gaucher n'entraine pas d'anomalie de la fertilite. En revanche, le risque d'avortement spontane est plus important que dans la population generale. L'evolution de la MG pendant la grossesse est variable, fonction de la severite de la ma
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1c36ee97245ca68ce0dc5120025c385f
https://doi.org/10.1016/s0755-4982(09)73663-2
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