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Items: 1 to 20 of 64


Multifocal electroretinogram findings in sickle cell maculopathy.

Beral L, Romana M, Lemonne N, Garnier Y, Billaud M, Acomat M, Zorobabel C, Etienne-Julan M, David T, Connes P.

Eye (Lond). 2019 Jul 9. doi: 10.1038/s41433-019-0499-7. [Epub ahead of print]


Proliferative retinopathy and maculopathy are two independent conditions in sickle cell disease: Is there a role of blood rheology?1.

Beral L, Lemonne N, Romana M, Charlot K, Billaud M, Acomat M, Zorobabel C, Nader E, Etienne-Julan M, David T, Connes P.

Clin Hemorheol Microcirc. 2019;71(3):337-345. doi: 10.3233/CH-180412.


Lipid profiles in French West Indies sickle cell disease cohorts, and their general population.

Lalanne-Mistrih ML, Connes P, Lamarre Y, Lemonne N, Hardy-Dessources MD, Tarer V, Etienne-Julan M, Mougenel D, Tressières B, Romana M.

Lipids Health Dis. 2018 Mar 5;17(1):38. doi: 10.1186/s12944-018-0689-5.


Prevalence of sickle cell disease among Grenadian newborns.

Antoine M, Lee K, Donald T, Belfon Y, Drigo A, Polson S, Martin F, Mitchell G, Etienne-Julan M, Hardy-Dessources MD.

J Med Screen. 2018 Mar;25(1):49-50. doi: 10.1177/0969141317695356. Epub 2017 Mar 24.


Design of the DREPAGREFFE trial: A prospective controlled multicenter study evaluating the benefit of genoidentical hematopoietic stem cell transplantation over chronic transfusion in sickle cell anemia children detected to be at risk of stroke by transcranial Doppler (NCT 01340404).

Chevret S, Verlhac S, Ducros-Miralles E, Dalle JH, de Latour RP, de Montalembert M, Benkerrou M, Pondarré C, Thuret I, Guitton C, Lesprit E, Etienne-Julan M, Elana G, Vannier JP, Lutz P, Neven B, Galambrun C, Paillard C, Runel C, Jubert C, Arnaud C, Kamdem A, Brousse V, Missud F, Petras M, Doumdo-Divialle L, Berger C, Fréard F, Taieb O, Drain E, Elmaleh M, Vasile M, Khelif Y, Bernaudin M, Chadebech P, Pirenne F, Socié G, Bernaudin F.

Contemp Clin Trials. 2017 Nov;62:91-104. doi: 10.1016/j.cct.2017.08.008. Epub 2017 Aug 15.


Effects of hydroxyurea on blood rheology in sickle cell anemia: A two-years follow-up study.

Lemonne N, Möckesch B, Charlot K, Garnier Y, Waltz X, Lamarre Y, Antoine-Jonville S, Etienne-Julan M, Hardy-Dessources MD, Romana M, Connes P.

Clin Hemorheol Microcirc. 2017;67(2):141-148. doi: 10.3233/CH-170280.


Decrease of externalized phosphatidylserine density on red blood cell-derived microparticles in SCA patients treated with hydroxycarbamide.

Garnier Y, Ferdinand S, Connes P, Garnier M, Etienne-Julan M, Lemonne N, Romana M.

Br J Haematol. 2018 Aug;182(3):448-451. doi: 10.1111/bjh.14810. Epub 2017 Jun 27. No abstract available.


Differences of microparticle patterns between sickle cell anemia and hemoglobin SC patients.

Garnier Y, Ferdinand S, Etienne-Julan M, Elana G, Petras M, Doumdo L, Tressières B, Lalanne-Mistrih ML, Hardy-Dessources MD, Connes P, Romana M.

PLoS One. 2017 May 10;12(5):e0177397. doi: 10.1371/journal.pone.0177397. eCollection 2017.


Association between oxidative stress and vascular reactivity in children with sickle cell anaemia and sickle haemoglobin C disease.

Möckesch B, Connes P, Charlot K, Skinner S, Hardy-Dessources MD, Romana M, Jumet S, Petras M, Divialle-Doumdo L, Martin C, Tressières B, Tarer V, Hue O, Etienne-Julan M, Antoine S, Pialoux V.

Br J Haematol. 2017 Aug;178(3):468-475. doi: 10.1111/bjh.14693. Epub 2017 May 3.


Cerebral and muscle microvascular oxygenation in children with sickle cell disease: Influence of hematology, hemorheology and vasomotion.

Charlot K, Antoine-Jonville S, Moeckesch B, Jumet S, Romana M, Waltz X, Divialle-Doumdo L, Hardy-Dessources MD, Petras M, Tressières B, Tarer V, Hue O, Etienne-Julan M, Connes P.

Blood Cells Mol Dis. 2017 Jun;65:23-28. doi: 10.1016/j.bcmd.2017.03.015. Epub 2017 Apr 4.


Micro- and macrovascular function in children with sickle cell anaemia and sickle cell haemoglobin C disease.

Möckesch B, Charlot K, Jumet S, Romana M, Divialle-Doumdo L, Hardy-Dessources MD, Petras M, Tressieres B, Tarer V, Hue O, Etienne-Julan M, Connes P, Antoine-Jonville S.

Blood Cells Mol Dis. 2017 May;64:23-29. doi: 10.1016/j.bcmd.2017.02.001. Epub 2017 Feb 4.


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.

Pediatr Blood Cancer. 2017 Aug;64(8). doi: 10.1002/pbc.26455. Epub 2017 Jan 18.


Exacerbation of oxidative stress during sickle vaso-occlusive crisis is associated with decreased anti-band 3 autoantibodies rate and increased red blood cell-derived microparticle level: a prospective study.

Hierso R, Lemonne N, Villaescusa R, Lalanne-Mistrih ML, Charlot K, Etienne-Julan M, Tressières B, Lamarre Y, Tarer V, Garnier Y, Hernandez AA, Ferracci S, Connes P, Romana M, Hardy-Dessources MD.

Br J Haematol. 2017 Mar;176(5):805-813. doi: 10.1111/bjh.14476. Epub 2016 Dec 16.


Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study.

Renoux C, Romana M, Joly P, Ferdinand S, Faes C, Lemonne N, Skinner S, Garnier N, Etienne-Julan M, Bertrand Y, Petras M, Cannas G, Divialle-Doumdo L, Nader E, Cuzzubbo D, Lamarre Y, Gauthier A, Waltz X, Kebaili K, Martin C, Hot A, Hardy-Dessources MD, Pialoux V, Connes P.

PLoS One. 2016 Jun 29;11(6):e0158182. doi: 10.1371/journal.pone.0158182. eCollection 2016.


Men with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate Strength.

Cita KC, Brureau L, Lemonne N, Billaud M, Connes P, Ferdinand S, Tressières B, Tarer V, Etienne-Julan M, Blanchet P, Elion J, Romana M.

PLoS One. 2016 May 4;11(5):e0154866. doi: 10.1371/journal.pone.0154866. eCollection 2016.


Association of adenylyl cyclase 6 rs3730070 polymorphism and hemolytic level in patients with sickle cell anemia.

Cita KC, Ferdinand S, Connes P, Brudey L, Tressières B, Etienne-Julan M, Lemonne N, Tarer V, Elion J, Romana M.

Blood Cells Mol Dis. 2016 May;58:21-5. doi: 10.1016/j.bcmd.2016.02.006. Epub 2016 Feb 18.


Changes in autonomic nervous activity during vaso-occlusive crisis in patients with sickle cell anaemia.

Charlot K, Hierso R, Lemonne N, Romana M, Tressières B, Lalanne-Mistrih ML, Etienne-Julan M, Tarer V, Ferracci S, Hardy-Dessources MD, Connes P.

Br J Haematol. 2017 May;177(3):484-486. doi: 10.1111/bjh.14064. Epub 2016 Mar 24. No abstract available.


CAREST--Multilingual Regional Integration for Health Promotion and Research on Sickle Cell Disease and Thalassemia.

Knight-Madden J, Romana M, Villaescusa R, Reid M, Etienne-Julan M, Boutin L, Elana G, Elenga N, Wheeler G, Lee K, Nieves R, Jones Lecointe A, Lalanne-Mistrih ML, Loko G, Keclard-Christophe L, Hardy-Dessources MD.

Am J Public Health. 2016 May;106(5):851-3. doi: 10.2105/AJPH.2016.303078. Epub 2016 Mar 21.


Which side of the balance determines the frequency of vaso-occlusive crises in children with sickle cell anemia: Blood viscosity or microvascular dysfunction?

Charlot K, Romana M, Moeckesch B, Jumet S, Waltz X, Divialle-Doumdo L, Hardy-Dessources MD, Petras M, Tressières B, Tarer V, Hue O, Etienne-Julan M, Antoine-Jonville S, Connes P.

Blood Cells Mol Dis. 2016 Jan;56(1):41-5. doi: 10.1016/j.bcmd.2015.10.005. Epub 2015 Nov 7.


Impact of eNOS polymorphisms on red blood cell aggregation in sickle cell disease.

Ferdinand S, Connes P, Brudey L, Cita KC, Tressières B, Lemonne N, Hardy-Dessources MD, Lamarre Y, Waltz X, Etienne-Julan M, Romana M.

Blood Cells Mol Dis. 2015 Aug;55(2):151-3. doi: 10.1016/j.bcmd.2015.05.008. Epub 2015 May 27. No abstract available.

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