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Items: 1 to 20 of 81

1.

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]

PMID:
31289356
2.

Terminologies regarding sickle cell retinopathy and maculopathy.

Beral L, Romana M, Lemonne N, David T, Connes P.

Clin Hemorheol Microcirc. 2019;71(1):1-2. doi: 10.3233/CH-190552. No abstract available.

PMID:
30714953
3.

New insights into red cell rheology and adhesion in patients with sickle cell anaemia during vaso-occlusive crises.

Lapoumeroulie C, Connes P, El Hoss S, Hierso R, Charlot K, Lemonne N, Elion J, Le Van Kim C, Romana M, Hardy-Dessources MD.

Br J Haematol. 2019 Jun;185(5):991-994. doi: 10.1111/bjh.15686. Epub 2018 Nov 22. No abstract available.

PMID:
30467840
4.

Hydroxyurea therapy modulates sickle cell anemia red blood cell physiology: Impact on RBC deformability, oxidative stress, nitrite levels and nitric oxide synthase signalling pathway.

Nader E, Grau M, Fort R, Collins B, Cannas G, Gauthier A, Walpurgis K, Martin C, Bloch W, Poutrel S, Hot A, Renoux C, Thevis M, Joly P, Romana M, Guillot N, Connes P.

Nitric Oxide. 2018 Dec 1;81:28-35. doi: 10.1016/j.niox.2018.10.003. Epub 2018 Oct 19.

PMID:
30342855
5.

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.

PMID:
29865045
6.

Microparticles in sickle cell disease.

Romana M, Connes P, Key NS.

Clin Hemorheol Microcirc. 2018;68(2-3):319-329. doi: 10.3233/CH-189014.

PMID:
29614639
7.

Blood rheological abnormalities in sickle cell anemia.

Connes P, Renoux C, Romana M, Abkarian M, Joly P, Martin C, Hardy-Dessources MD, Ballas SK.

Clin Hemorheol Microcirc. 2018;68(2-3):165-172. doi: 10.3233/CH-189005.

PMID:
29614630
8.

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.

9.

Association between Oxidative Stress, Genetic Factors, and Clinical Severity in Children with Sickle Cell Anemia.

Renoux C, Joly P, Faes C, Mury P, Eglenen B, Turkay M, Yavas G, Yalcin O, Bertrand Y, Garnier N, Cuzzubbo D, Gauthier A, Romana M, Möckesch B, Cannas G, Antoine-Jonville S, Pialoux V, Connes P.

J Pediatr. 2018 Apr;195:228-235. doi: 10.1016/j.jpeds.2017.12.021. Epub 2018 Feb 13.

PMID:
29449005
10.

Band 3 phosphorylation induces irreversible alterations of stored red blood cells.

Azouzi S, Romana M, Arashiki N, Takakuwa Y, El Nemer W, Peyrard T, Colin Y, Amireault P, Le Van Kim C.

Am J Hematol. 2018 May;93(5):E110-E112. doi: 10.1002/ajh.25044. Epub 2018 Feb 24. No abstract available.

11.

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.

PMID:
28759962
12.

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.

PMID:
28653368
13.

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.

14.

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.

PMID:
28466542
15.

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.

PMID:
28411485
16.

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.

PMID:
28340403
17.

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.

PMID:
28097791
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.

PMID:
27984639
19.

UGT1A1 (TA)n genotype is not the major risk factor of cholelithiasis in sickle cell disease children.

Joly P, Renoux C, Lacan P, Bertrand Y, Cannas G, Garnier N, Cuzzubbo D, Kebaïli K, Renard C, Gauthier A, Pialoux V, Martin C, Romana M, Connes P.

Eur J Haematol. 2017 Mar;98(3):296-301. doi: 10.1111/ejh.12838. Epub 2017 Jan 9.

PMID:
27981643
20.

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.

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