Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Isabelle Hagège"'
Autor:
Léon Tshilolo, Cécile Toly-Ndour, Anne-Marie Rouquette, Pauline M’Bappe, Robert Girot, Isabelle Hagège, Faiza Boussa-Khettab, François Lionnet, Stéphanie Obadia
Publikováno v:
The Journal of Rheumatology. 38:302-309
Objective.Frequency and titers of autoantibodies in patients with sickle-cell disease (SCD) have been reported as relatively high. In a prospective study of 88 patients, we examined this “hyper-autoreactivity” and its clinical consequences.Method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66d53520362bfb898e68cf9b618635cf
https://doi.org/10.3899/jrheum.100667
https://doi.org/10.3899/jrheum.100667
Autor:
N. Bouchaïr, A. Verschuur, P. Raphalen, Micheline Maier-Redelsperger, Robert Girot, A. Kanfer, M. de Montalembert, Isabelle Hagège, P. Manigne
Publikováno v:
Archives de Pédiatrie. 7:249-255
Resume Objectif Reduire la frequence des crises douloureuses drepanocytaires responsables d'hospitalisations, par des saignees induisant une diminution du taux d'hemoglobine et une carence en fer chez des patients dont le taux d'hemoglobine spontane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::465dd7aad61d5cf30c2cdd86bc02e89f
https://doi.org/10.1016/s0929-693x(00)88740-0
https://doi.org/10.1016/s0929-693x(00)88740-0
Autor:
Marie-Claude Simeoni, Vincent Barlogis, Anderson Loundou, Corinne Pondarré, Jean Donadieu, Mariane de Montalembert, Claire Berger, Marguerite Micheau, Dominique Steschenko, Christian Rose, Frédéric Galactéros, Laurence Lutz, Isabelle Thuret, Brigitte Pegourie, Catherine Badens, Françoise Bernaudin, Thierry Leblanc, Robert Girot, Isabelle Hagège, Dora Bachir
Publikováno v:
Haematologica. 95(5)
Background β-thalassemia is a rare disease in France, encountered mainly in patients originating from Italy and North Africa. In the setting of the recent French plan for rare diseases, a National Registry for thalassemia has been developed since 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84084d025d5151de6ff5d2a41f2282ff
https://pubmed.ncbi.nlm.nih.gov/20007138
https://pubmed.ncbi.nlm.nih.gov/20007138
Publikováno v:
Presse medicale (Paris, France : 1983). 39(7-8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f50996a0a195b3db31252ace1b8fe6e9
https://pubmed.ncbi.nlm.nih.gov/20207101
https://pubmed.ncbi.nlm.nih.gov/20207101
Autor:
Stanislas Pol, Xavier Amiot, Armand Garioud, David Ancel, Robert Girot, Jean-Didier Grangé, Isabelle Hagège, Dominique Chaslin-Ferbus
Publikováno v:
European journal of gastroenterologyhepatology. 21(7)
Hepatic complications are a major cause of death in patients with congenital anaemia and chronic hepatitis C. Ribavirin is usually contraindicated in patients with haemolytic anaemia. This pilot study evaluated the efficacy and safety of antiviral tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3f7160ae8c6c49b38cf979723170657
https://pubmed.ncbi.nlm.nih.gov/20440118
https://pubmed.ncbi.nlm.nih.gov/20440118
Autor:
Sandrine Placier, Alain Kanfer, Jean-Claude Dussaule, Pierre-Louis Tharaux, Michel Vayssairat, Robert Girot, Isabelle Hagège
Publikováno v:
Nephrology Dialysis Transplantation
Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2005, 20, pp.2408-13. ⟨10.1093/ndt/gfi111⟩
Nephrology Dialysis Transplantation, Oxford University Press, 2005, 20, pp.2408-13. ⟨10.1093/ndt/gfi111⟩
Nephrology Dialysis Transplantation, 2005, 20, pp.2408-13. ⟨10.1093/ndt/gfi111⟩
Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2005, 20, pp.2408-13. ⟨10.1093/ndt/gfi111⟩
Nephrology Dialysis Transplantation, Oxford University Press, 2005, 20, pp.2408-13. ⟨10.1093/ndt/gfi111⟩
Nephrology Dialysis Transplantation, 2005, 20, pp.2408-13. ⟨10.1093/ndt/gfi111⟩
BACKGROUND: Sickle cell disease (SCD) affects the kidney by acute mechanisms as well as by insidious renal medullary/papillary necrosis, resulting in tubular defects, which increase the risk of dehydration and subsequent sickle crisis. Hypoxia has be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97317bfd05f7780ec606293ff267eb13
https://www.hal.inserm.fr/inserm-00000115
https://www.hal.inserm.fr/inserm-00000115
Publikováno v:
La Presse Médicale. 39:849-850
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf8e79acc45dbd8e97725caee39b6ad7
https://doi.org/10.1016/j.lpm.2009.09.028
https://doi.org/10.1016/j.lpm.2009.09.028
Publikováno v:
European Journal of Haematology. 67:230-231
Objective Compliance with parenteral administration of deferoxamine is often poor in thalassemic patients with iron overload. We tested the efficacy and tolerance of the drug at high dosage 2 d per week for 24 months in two adult thalassemic patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bddf2b1507067555071f63ba98d7e13
https://doi.org/10.1034/j.1600-0609.2001.00386.x
https://doi.org/10.1034/j.1600-0609.2001.00386.x
Autor:
Pierre-Louis Tharaux, Isabelle Hagège, Sandrine Placier, Michel Vayssairat, Alain Kanfer, Robert Girot, Jean-Claude Dussaule
Publikováno v:
Nephrology Dialysis Transplantation; Nov2005, Vol. 20 Issue 11, p2408-2413, 6p
Publikováno v:
Bulletin de la Société Botanique de France. Lettres Botaniques. 132:195-202
ResumeLes cellules du mesophylle de Vicia faba L. sont isolees rapidement (30 a 40 min) par une methode enzymatique. Ces cellules peuvent etre ainsi utilisees pour l'etude des phenomenes d'absorption des nutriments avant l'apparition du phenomene de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17fb0a1fefb13739f6c0b02ca280eb52
https://doi.org/10.1080/01811797.1985.10824665
https://doi.org/10.1080/01811797.1985.10824665