Pierre Brissot
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Explore the profile of Pierre Brissot including associated specialties, affiliations and a list of published articles.
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121
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Recent Articles
1.
Alvarenga A, Brissot P, Santos P
World J Hepatol
. 2022 Dec;
14(11):1931-1939.
PMID: 36483608
Haemochromatosis is a genetic disease caused by hepcidin deficiency, responsible for an increase in intestinal iron absorption. Haemochromatosis is associated with homozygosity for the p.Cys282Tyr mutation. However, rare cases of...
2.
Acevedo L, Alvarenga A, Fonseca P, Silva N, Cancado R, Naoum F, et al.
Genes (Basel)
. 2022 Jan;
13(1).
PMID: 35052458
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...
3.
Girelli D, Busti F, Brissot P, Cabantchik I, Muckenthaler M, Porto G
Blood
. 2021 Oct;
139(20):3018-3029.
PMID: 34601591
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,...
4.
Brissot P, Brissot E
Clin Hematol Int
. 2021 Oct;
2(4):143-148.
PMID: 34595455
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...
5.
6.
Brissot E, Troadec M, Loreal O, Brissot P
Am J Hematol
. 2021 Apr;
96(8):1008-1016.
PMID: 33844865
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...
7.
Alvarenga A, Silva N, Fonseca P, Oliveira T, da Silva Monteiro J, Cancado R, et al.
Blood Cells Mol Dis
. 2020 May;
84:102444.
PMID: 32464486
Background: Five main genes are associated with hemochromatosis; however, current studies show that, in addition to these genes, others may be associated with primary iron overload (IO). One of these...
8.
Zhang W, Wang X, Duan W, Xu A, Zhao X, Huang J, et al.
Front Genet
. 2020 Mar;
11:77.
PMID: 32153640
-related Hemochromatosis is the most common genetic iron overload disease in European populations, particularly of Nordic or Celtic ancestry. It is reported that the p.C282Y mutation is present in 1/10...
9.
Brissot E, Bernard D, Loreal O, Brissot P, Troadec M
Blood Rev
. 2019 Nov;
39:100617.
PMID: 31753415
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...
10.
Kenawi M, Rouger E, Island M, Leroyer P, Robin F, Remy S, et al.
FASEB J
. 2019 Sep;
33(12):13492-13502.
PMID: 31560858
Hereditary aceruloplasminemia (HA), related to mutations in the ceruloplasmin () gene, leads to iron accumulation. Ceruloplasmin ferroxidase activity being considered essential for macrophage iron release, macrophage iron overload is expected,...