Etienne-Julan M - Search Results

1

Alpha-thalassaemia promotes frequent vaso-occlusive crises in children with sickle cell anaemia through haemorheological changes.

Renoux C, Connes P, Nader E, Skinner S, Faes C, Petras M, Bertrand Y, Garnier N, Cuzzubbo D, Divialle-Doumdo L, Kebaïli K, Renard C, Gauthier A, Etienne-Julan M, Cannas G, Martin C, Hardy-Dessources MD, Pialoux V, Romana M, Joly P. Renoux C, et al. Pediatr Blood Cancer. 2017 Aug;64(8). doi: 10.1002/pbc.26455. Epub 2017 Jan 18. Pediatr Blood Cancer. 2017. PMID: 28097791

2

[Analysis of hospitalization of adult sickle-cell patients in Guadeloupe].

Le Turdu-Chicot C, Foucan L, Etienne-Julan M, Leborgne-Samuel Y, Fanhan R, Berchel C. Le Turdu-Chicot C, et al. Rev Med Interne. 2000 Jan;21(1):24-9. doi: 10.1016/s0248-8663(00)87225-2. Rev Med Interne. 2000. PMID: 10685451 French.

3

Lactic response in sickle cell trait carriers in comparison with subjects with normal hemoglobin.

Sara F, Hardy-Dessources MD, Voltaire B, Etienne-Julan M, Hue O. Sara F, et al. Clin J Sport Med. 2003 Mar;13(2):96-101. doi: 10.1097/00042752-200303000-00006. Clin J Sport Med. 2003. PMID: 12629427

4

Childhood sickle cell crises: clinical severity, inflammatory markers and the role of interleukin-8.

Etienne-Julan M, Belloy MS, Decastel M, Dougaparsad S, Ravion S, Hardy-Dessources MD. Etienne-Julan M, et al. Haematologica. 2004 Jul;89(7):863-4. Haematologica. 2004. PMID: 15257940

5

Faster lactate transport across red blood cell membrane in sickle cell trait carriers.

Sara F, Connes P, Hue O, Montout-Hedreville M, Etienne-Julan M, Hardy-Dessources MD. Sara F, et al. J Appl Physiol (1985). 2006 Feb;100(2):427-32. doi: 10.1152/japplphysiol.00771.2005. Epub 2005 Oct 20. J Appl Physiol (1985). 2006. PMID: 16239612 Free article.

6

Does higher red blood cell (RBC) lactate transporter activity explain impaired RBC deformability in sickle cell trait?

Connes P, Sara F, Hardy-Dessources MD, Etienne-Julan M, Hue O. Connes P, et al. Jpn J Physiol. 2005 Dec;55(6):385-7. doi: 10.2170/jjphysiol.S653. Epub 2006 Jan 31. Jpn J Physiol. 2005. PMID: 16441976 Free article.

7

Sickle cell anemia in Guadeloupean children: pattern and prevalence of acute clinical events.

Tarer V, Etienne-Julan M, Diara JP, Belloy MS, Mukizi-Mukaza M, Elion J, Romana M. Tarer V, et al. Eur J Haematol. 2006 Mar;76(3):193-9. doi: 10.1111/j.1600-0609.2005.00590.x. Eur J Haematol. 2006. PMID: 16451394

8

UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia.

Chaar V, Kéclard L, Etienne-Julan M, Diara JP, Elion J, Krishnamoorthy R, Romana M. Chaar V, et al. Am J Hematol. 2006 May;81(5):377-9. doi: 10.1002/ajh.20574. Am J Hematol. 2006. PMID: 16628735 Free article.

9

ET-1 and ecNOS gene polymorphisms andsusceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemia.

Chaar V, Tarer V, Etienne-Julan M, Diara JP, Elion J, Romana M. Chaar V, et al. Haematologica. 2006 Sep;91(9):1277-8. Haematologica. 2006. PMID: 16956834

10

Ventilatory and lactic thresholds in subjects with sickle cell trait.

Marlin L, Sara F, Antoine-Jonville S, Connes P, Etienne-Julan M, Hue O. Marlin L, et al. Int J Sports Med. 2007 Nov;28(11):916-20. doi: 10.1055/s-2007-964983. Epub 2007 May 11. Int J Sports Med. 2007. PMID: 17497586

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