Zobrazeno 1 - 10
of 302
pro vyhledávání: '"Pierre, Brissot"'
Autor:
Pierre Brissot, Eolia Brissot
Publikováno v:
Clinical Hematology International, Vol 2, Iss 4 (2020)
Major advances in the understanding of genetic iron overload have led to a clarification of the nosology and terminology of the related diseases. The term hemochromatosis should be reserved to the entities where iron overload is related to hepcidin d
Externí odkaz:
https://doaj.org/article/8e24c150d1454d568fc8d4b7602f5118
Autor:
Wei Zhang, Xiaoming Wang, Weijia Duan, Anjian Xu, Xinyan Zhao, Jian Huang, Hong You, Pierre Brissot, Xiaojuan Ou, Jidong Jia
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
HFE-related Hemochromatosis is the most common genetic iron overload disease in European populations, particularly of Nordic or Celtic ancestry. It is reported that the HFE p.C282Y mutation is present in 1/10 people of northern European descent, resu
Externí odkaz:
https://doaj.org/article/c194f4d027a148b98e5e2f4bdd5ae695
Autor:
Paula Fernanda Silva Fonseca, Rodolfo Delfini Cançado, Flavio Augusto Naoum, Carla Luana Dinardo, Guilherme Henrique Hencklain Fonseca, Sandra Fatima Menosi Gualandro, José Eduardo Krieger, Alexandre Costa Pereira, Pierre Brissot, Paulo Caleb Junior Lima Santos
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)
Abstract Background Hereditary hemochromatosis (HH) encompasses a group of autosomal recessive disorders mainly characterized by enhanced intestinal absorption of iron and its accumulation in parenchymal organs. HH diagnosis is based on iron biochemi
Externí odkaz:
https://doaj.org/article/43e123d81f7c4a6bb4f7d80d50b831ff
Publikováno v:
American Journal of Hematology
American Journal of Hematology, 2021, 96 (8), pp.1008-1016. ⟨10.1002/ajh.26189⟩
American Journal of Hematology, Wiley, 2021, 96 (8), pp.1008-1016. ⟨10.1002/ajh.26189⟩
American Journal of Hematology, 2021, 96 (8), pp.1008-1016. ⟨10.1002/ajh.26189⟩
American Journal of Hematology, Wiley, 2021, 96 (8), pp.1008-1016. ⟨10.1002/ajh.26189⟩
No data; International audience; The role of iron in the formation and functioning of erythrocytes, and to a lesser degree of white blood cells, is well established, but the relationship between iron and platelets is less documented. Physiologically,
Autor:
Pierre Brissot, Ioav Cabantchik, Fabiana Busti, Domenico Girelli, Martina U. Muckenthaler, Graça Porto
Publikováno v:
Blood
Blood, 2022, 139 (20), pp.3018-3029. ⟨10.1182/blood.2021011338⟩
Blood, American Society of Hematology, 2021, ⟨10.1182/blood.2021011338⟩
Blood, 2022, 139 (20), pp.3018-3029. ⟨10.1182/blood.2021011338⟩
Blood, American Society of Hematology, 2021, ⟨10.1182/blood.2021011338⟩
Hemochromatosis (HC) is a genetically heterogeneous disorder in which uncontrolled intestinal iron absorption may lead to progressive iron overload (IO) responsible for disabling and life-threatening complications such as arthritis, diabetes, heart f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::416d5dcdc653ae0cf8a7c0ae40fc56d9
https://hal.science/hal-03418911/document
https://hal.science/hal-03418911/document
Publikováno v:
World journal of hepatology
World journal of hepatology, 2022, 14 (11), pp.1931-1939. ⟨10.4254/wjh.v14.i11.1931⟩
World journal of hepatology, 2022, 14 (11), pp.1931-1939. ⟨10.4254/wjh.v14.i11.1931⟩
International audience; Haemochromatosis is a genetic disease caused by hepcidin deficiency, responsible for an increase in intestinal iron absorption. Haemochromatosis is associated with homozygosity for the HFE p.Cys282Tyr mutation. However, rare c
Autor:
Luis Alfredo Utria Acevedo, Aline Morgan Alvarenga, Paula Fernanda Silva Fonseca, Nathália Kozikas da Silva, Rodolfo Delfini Cançado, Flavio Augusto Naoum, Carla Luana Dinardo, Alexandre Costa Pereira, Pierre Brissot, Paulo Caleb Junior Lima Santos
Publikováno v:
Genes
Genes, 2022, 13 (1), pp.118. ⟨10.3390/genes13010118⟩
Genes, Vol 13, Iss 118, p 118 (2022)
Genes; Volume 13; Issue 1; Pages: 118
Genes, 2022, 13 (1), pp.118. ⟨10.3390/genes13010118⟩
Genes, Vol 13, Iss 118, p 118 (2022)
Genes; Volume 13; Issue 1; Pages: 118
Background: Hemochromatosis is a genetic condition of iron overload caused by deficiency of hepcidin. In a previous stage of this study, patients with suspected hemochromatosis had their quality of life (QL) measured. We observed that QL scores diffe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02abae0cd656846cfdc08d0a42e03e17
https://hal.science/hal-03555426/document
https://hal.science/hal-03555426/document
Autor:
Olivier Loréal, Thibault Cavey, François Robin, Moussa Kenawi, Pascal Guggenbuhl, Pierre Brissot
Publikováno v:
Pharmaceuticals, Vol 11, Iss 4, p 131 (2018)
Genetic hemochromatosis is an iron overload disease that is mainly related to the C282Y mutation in the HFE gene. This gene controls the expression of hepcidin, a peptide secreted in plasma by the liver and regulates systemic iron distribution. Homoz
Externí odkaz:
https://doaj.org/article/3d022d849a074cc19f272546e8aeb2e7
Autor:
Pierre Brissot, Olivier Loreal
Publikováno v:
Thalassemia Reports, Vol 4, Iss 3 (2014)
Liver complications in haemoglobinopathies (thalassaemia and sickle cell disease) are due to several factors, dominated (beside chronic viral infections, not considered here) by chronic iron overload, biliary obstruction and venous thrombosis. Wherea
Externí odkaz:
https://doaj.org/article/679c76b64af34245a12a989872f3408d
Publikováno v:
Blood Reviews
Blood Reviews, Elsevier, 2020, 39, pp.100617. ⟨10.1016/j.blre.2019.100617⟩
Blood Reviews, 2020, 39, pp.100617. ⟨10.1016/j.blre.2019.100617⟩
Blood Reviews, Elsevier, 2020, 39, pp.100617. ⟨10.1016/j.blre.2019.100617⟩
Blood Reviews, 2020, 39, pp.100617. ⟨10.1016/j.blre.2019.100617⟩
International audience; The role of iron in non-erythroid hematopoietic lineages and its implication in hemato-oncogenesis are still debated. Iron exerts an important role on hematopoietic stem cell transformation and on mature white blood cell diffe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c4effc8823f031404c908ba6b5f91ad
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02472239
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02472239