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The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait]

Autor: Dora Bachir, P. Colonna, E Dorleac, Nicole Alloisio, O. Gentilhomme, L Morle, L Roda, D. Guetarni, M. Bost, Z Zouaoui

Publikováno v: Blood. 65:46-51

Using clinical, morphological, genetic, and biochemical criteria, we studied ten white and North African families with hereditary elliptocytosis (HE). In four families, elliptocytic individuals displayed a highly significant reduction of band 4.1, wh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02e663798a46ae747e4438f33de8ac8b
https://doi.org/10.1182/blood.v65.1.46.bloodjournal65146

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Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia

Autor: D Peyramond, F Baklouti, Jacques Delaunay, E Dorleac, J Godet, L Morle, P Laselve, M Aubry

Publikováno v: Blood. 67:957-961

Hb Knossos (beta 27 (B9) Ala----Ser) is a recently discovered hemoglobin variant endowed with beta-thalassemic properties (1,2) We present the first homozygous cases. The propositus, a 19-year-old man is originally from northeast Algeria, but is unre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74538ca94fbb9990daf17a329045656c
https://doi.org/10.1182/blood.v67.4.957.957

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[Course and surveillance of severe injuries of the pancreas. Apropos of 3 cases followed for more than 15 years. Value of fluorescein dilaurate and glycosylated hemoglobin]

Autor: G, Spay, J, Forichon, A, Francina, E, Dorleac, G, Maret, X, Delore

Publikováno v: Chirurgie; memoires de l'Academie de chirurgie. 112(1)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::41e8be5e55730a6ae34b6af697c7d413
https://pubmed.ncbi.nlm.nih.gov/3677898

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Hb Lepore-Hb C and Hb Lepore-beta 0-thalassemia compound heterozygotes in an Algerian family

Autor: A, Francina, E, Dorleac, M, Aubry, F, Baklouti, S, Elwan, L, Roda, N, Phillipe, J, Delaunay

Publikováno v: Hemoglobin. 9(5)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8792ca5b8cf088553a5dc27d50713c8b
https://pubmed.ncbi.nlm.nih.gov/4086305

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[Peptidoglycan modification of Staphylococcus aureus P18 strain after use of 6 active antibiotics on the bacterial wall]

Autor: F, Najioullah, J, Freney, G, Pellon, H, Meugnier, E, Dorleac, C, Durand, J, Fleurette

Publikováno v: Pathologie-biologie. 37(5)

Six antibiotics active on the cell-wall were tested against a methicillin resistant Staphylococcus aureus P18 strain at the start of exponential growth rate. The concentration was four-fold the MIC determined in a non-hypersaline liquid medium. The p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5b8e6491a656b427b839f9dd2916afbc
https://pubmed.ncbi.nlm.nih.gov/2780093

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Carrier-ampholyte displacement chromatography (chromatofocusing) on ion-exchange papers. Application to the separation of haemoglobin variants

Autor: A, Francina, E, Dorleac, H, Cloppet

Publikováno v: Journal of chromatography. 222(1)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ce39d412b7d6f37f2eeeb93f7effb2ed
https://pubmed.ncbi.nlm.nih.gov/7217317

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[Apolipoproteins and glycosylated hemoglobin in the young insulin-dependent diabetic]

Autor: L, Richard, J, Delaunay, E, Dorleac, P, Gillet

Publikováno v: Archives francaises de pediatrie. 40(1)

Apolipoproteins A and B, total cholesterol, triglycerides, HDL, LDL, VLDL cholesterol and glycosylated hemoglobin levels were measured in 81 children and adolescents with juvenile-onset diabetes. There were 41 males and 40 females aged 7 to 22 years.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0701a31361d015b63ef7ca490e3ca9a8
https://pubmed.ncbi.nlm.nih.gov/6860065

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The genetic abnormalities involving red cell membrane protein 4.1 with or without elliptocytosis

Autor: N, Alloisio, E, Dorleac, L, Morle, R, Girot, C, Galant, P, Boivin, J, Delaunay

Publikováno v: Biomedica biochimica acta. 42(11-12)

We have studied 20 caucasian individuals including 3 independent persons and 17 persons belonging to 6 unrelated families. These subjects are normal or elliptocytic. On biochemical grounds, families with hereditary elliptocytosis (HE) can be divided

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6bf28d4a911cc8953c0a30b8340ec443
https://pubmed.ncbi.nlm.nih.gov/6675716

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Alpha-globin gene deletions associated with alpha A and alpha G Philadelphia in an Algerian family that includes two Hb G homozygotes

Autor: F, Morle, P, Jaccoud, E, Dorleac, M, Motta, J, Delaunay, J, Godet

Publikováno v: Human genetics. 65(3)

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=pmid________::5338c4b2c56cd13605d707ec119a13a6
https://pubmed.ncbi.nlm.nih.gov/6199285

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