Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Evelyne Dorléac"'
Autor:
Jean Delaunay, Jacqueline Godet, François Morlé, Evelyne Dorléac, Claire Baudonnet, L Morle, Faouzi Baklouti
Publikováno v:
Scandinavian Journal of Haematology. 33:281-287
We report on a Moroccan family in which the proposita displays a picture of beta-thalassaemia intermedia, associated with heterozygous Hb O-Arab (beta 121 Glu----Lys) and a beta zero-thalassaemia trait. Hb O-Arab was ascertained by the disappearance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fcdee7d03175b89875d2dde2263ae21
https://doi.org/10.1111/j.1600-0609.1984.tb02229.x
https://doi.org/10.1111/j.1600-0609.1984.tb02229.x
Autor:
Jean Delaunay, L Morle, Evelyne Dorléac, Paul A Bryon, Genevieve Margueritte, Paule Jaccoud, Nicole Alloisio, N Philippe
Publikováno v:
Pediatric Research. 16:1016-1021
Red cell membrane proteins were investigated in two unrelated children with congenital dyserythropoietic anemia (CDA) I and two siblings with CDA II. The CDA I patients displayed globin chain synthesis imbalance, with reduction of the non alpha/alpha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7b39fe4630c40f2a5b345390361de54
https://doi.org/10.1203/00006450-198212000-00010
https://doi.org/10.1203/00006450-198212000-00010
Publikováno v:
Human Genetics. 65:303-307
An Algerian family with a high degree of consanguinity and including two homozygotes for Hb-G Philadelphia is presented. Whether homozygotes or heterozygotes, all subjects displayed microcytosis (with various degrees of poikilocytosis) and a moderate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49d4a9a60a7609707d61f9aff041abe2
https://doi.org/10.1007/bf00286523
https://doi.org/10.1007/bf00286523
Publikováno v:
Human Genetics. 59:68-71
In a 12-year-old boy carrying a clinically silent elliptocytosis, we observed a total lack of red cell membrane band 4.1. Band 4.1 was partially absent in the father who also displayed a clinically silent elliptocytosis and, remarkably, in the mother
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7a5b3b04b729791bd922042e3e7fc9a
https://doi.org/10.1007/bf00278857
https://doi.org/10.1007/bf00278857
Publikováno v:
American Journal of Hematology. 16:207-217
In recent studies, we observed a decrease of KMapp, an abnormally biphasic kinetics of the red cell membrane neutral phosphatase and an increased binding of hemoglobin to the membrane in various forms of beta-thalassemia. Since the gene encoding the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b959b648b957cafd2855bdb85831dff0
https://doi.org/10.1002/ajh.2830160302
https://doi.org/10.1002/ajh.2830160302
Various hemoglobins have been submitted to chromatofocusing on anion exchangers. This procedure gave a clear-cut separation of HbA2, HbF and HbA. A miniaturized method was suitable for routine HbA2 determination. In particular, it lead to the detecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ed1cbfab258dc75dc284c15aba30062
https://doi.org/10.1016/b978-0-08-029815-3.50139-2
https://doi.org/10.1016/b978-0-08-029815-3.50139-2
Autor:
Evelyne Dorléac, Jacques Delaunay, Dora Bachir, P. Jaccoud, Nicole Alloisio, P. Colonna, L Morle
Publikováno v:
American journal of hematology. 13(4)
We studied the red cell membrane neutral phosphatase, which is part of the Na+K+ ATPase, in several types of oxidative hemolytic anemias. We used an artificial substrate, the p-nitrophenylphosphate. In controls and in patients heterozygous for variou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2067078d4db42239f8595eee355be49
https://pubmed.ncbi.nlm.nih.gov/6297297
https://pubmed.ncbi.nlm.nih.gov/6297297
Autor:
Jean Delaunay, Faouzi Baklouti, Alain Francina, Georges Richard, Evelyne Dorléac, J Godet, Daniel Rosenberg
Publikováno v:
American journal of hematology. 26(3)
A Moroccan woman was investigated because of a typical beta-thalassemia trait associated with a low-percentage (11%) hemoglobin (Hb) variant. The beta-thalassemia trait was manifested by a microcytosis, a high HbA2 (above 6%), and an increase of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::027cc5061b4b246ed633adce783c93e2
https://pubmed.ncbi.nlm.nih.gov/3674004
https://pubmed.ncbi.nlm.nih.gov/3674004
Autor:
Henri Wajcman, Evelyne Dorléac, Jean Delaunay, Germaine Gombaud-Saintonge, J Godet, Henri Plauchu, Alain Francina, Faouzi Baklouti, V. Baudin-Chich
Publikováno v:
American journal of hematology. 27(4)
We report on the association of Hb Dunn (alpha 6[A4]Asp----Asn) and Hb O-Arab (beta 121 [GH4]Glu----Lys) in a healthy Moroccan man. Hb Dunn had the same electrophoretic properties as Hb G-Philadelphia, but its percentage was lower. Its identification
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a8aaf02bdb7de6a036146ddd8a43311
https://pubmed.ncbi.nlm.nih.gov/3354560
https://pubmed.ncbi.nlm.nih.gov/3354560