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Items: 1 to 50 of 86

1.

Blood Rheology: Key Parameters, Impact on Blood Flow, Role in Sickle Cell Disease and Effects of Exercise.

Nader E, Skinner S, Romana M, Fort R, Lemonne N, Guillot N, Gauthier A, Antoine-Jonville S, Renoux C, Hardy-Dessources MD, Stauffer E, Joly P, Bertrand Y, Connes P.

Front Physiol. 2019 Oct 17;10:1329. doi: 10.3389/fphys.2019.01329. eCollection 2019. Review.

2.

Metabolic response to oral glucose tolerance test performed in neutral and warm environmental temperature.

Antoine-Jonville S, El Khoury D, Faure C, Charlot K, Hue O, Hardy-Dessources MD.

Int J Hyperthermia. 2019;36(1):625-631.

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.

Point-of-care screening for sickle cell disease in low-resource settings: A multi-center evaluation of HemoTypeSC, a novel rapid test.

Steele C, Sinski A, Asibey J, Hardy-Dessources MD, Elana G, Brennan C, Odame I, Hoppe C, Geisberg M, Serrao E, Quinn CT.

Am J Hematol. 2019 Jan;94(1):39-45. doi: 10.1002/ajh.25305. Epub 2018 Oct 31.

5.

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
6.

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.

7.

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.

PMID:
29183229
8.

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
9.

Plasmapheresis may improve clinical condition in sickle cell disease through its effects on red blood cell rheology.

Nader E, Connes P, Lamarre Y, Renoux C, Joly P, Hardy-Dessources MD, Cannas G, Lemonne N, Ballas SK.

Am J Hematol. 2017 Nov;92(11):E629-E630. doi: 10.1002/ajh.24870. Epub 2017 Aug 17. No abstract available.

10.

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.

11.

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
12.

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
13.

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
14.

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
15.

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
16.

Effect of heat exposure and exercise on food intake regulation: A randomized crossover study in young healthy men.

Faure C, Charlot K, Henri S, Hardy-Dessources MD, Hue O, Antoine-Jonville S.

Metabolism. 2016 Oct;65(10):1541-9. doi: 10.1016/j.metabol.2016.07.004. Epub 2016 Jul 11.

PMID:
27621189
17.

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.

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.

PMID:
27009926
19.

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.

20.

Impaired glucose tolerance after brief heat exposure: a randomized crossover study in healthy young men.

Faure C, Charlot K, Henri S, Hardy-Dessources MD, Hue O, Antoine-Jonville S.

Clin Sci (Lond). 2016 Jun 1;130(12):1017-25. doi: 10.1042/CS20150461. Epub 2016 Mar 15.

PMID:
26980346
21.

Red blood cell nitric oxide synthase modulates red blood cell deformability in sickle cell anemia.

Mozar A, Connes P, Collins B, Hardy-Dessources MD, Romana M, Lemonne N, Bloch W, Grau M.

Clin Hemorheol Microcirc. 2016 Nov 4;64(1):47-53.

PMID:
26890236
22.

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.

PMID:
26603723
23.

Pfaffia paniculata extract improves red blood cell deformability in sickle cell patients.

Mozar A, Charlot K, Sandor B, Rabaï M, Lemonne N, Billaud M, Hardy-Dessources MD, Beltan E, Pandey RC, Connes P, Ballas SK.

Clin Hemorheol Microcirc. 2015 Sep 25;62(4):327-33. doi: 10.3233/CH-151972.

PMID:
26444603
24.

The role of blood rheology in sickle cell disease.

Connes P, Alexy T, Detterich J, Romana M, Hardy-Dessources MD, Ballas SK.

Blood Rev. 2016 Mar;30(2):111-8. doi: 10.1016/j.blre.2015.08.005. Epub 2015 Aug 28. Review.

25.

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.

26.

Physical activity level is not a determinant of autonomic nervous system activity and clinical severity in children/adolescents with sickle cell anemia: A pilot study.

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

Pediatr Blood Cancer. 2015 Nov;62(11):1962-7. doi: 10.1002/pbc.25604. Epub 2015 May 19.

PMID:
25989908
27.

Blood thixotropy in patients with sickle cell anaemia: role of haematocrit and red blood cell rheological properties.

Vent-Schmidt J, Waltz X, Romana M, Hardy-Dessources MD, Lemonne N, Billaud M, Etienne-Julan M, Connes P.

PLoS One. 2014 Dec 11;9(12):e114412. doi: 10.1371/journal.pone.0114412. eCollection 2014.

28.

Red blood cell nitric oxide synthase activation is increased in patients with sickle cell hemoglobin C disease.

Mozar A, Grau M, Lamarre Y, Weyel L, Suhr F, Collins B, Hardy-Dessources MD, Romana M, Lemonne N, Etienne-Julan M, Bloch W, Connes P.

Am J Hematol. 2015 Feb;90(2):E30-2. doi: 10.1002/ajh.23894. No abstract available.

29.

High red blood cell nitric oxide synthase activation is not associated with improved vascular function and red blood cell deformability in sickle cell anaemia.

Grau M, Mozar A, Charlot K, Lamarre Y, Weyel L, Suhr F, Collins B, Jumet S, Hardy-Dessources MD, Romana M, Lemonne N, Etienne-Julan M, Antoine-Jonville S, Bloch W, Connes P.

Br J Haematol. 2015 Mar;168(5):728-36. doi: 10.1111/bjh.13185. Epub 2014 Oct 15.

PMID:
25316332
30.

Impaired oxygen uptake efficiency slope and off-transient kinetics of pulmonary oxygen uptake in sickle cell anemia are associated with hemorheological abnormalities.

Charlot K, Waltz X, Hedreville M, Sinnapah S, Lemonne N, Etienne-Julan M, Soter V, Hue O, Hardy-Dessources MD, Connes P.

Clin Hemorheol Microcirc. 2015;60(4):413-21. doi: 10.3233/CH-141891.

PMID:
25261432
31.

Effects of oxidative stress on red blood cell rheology in sickle cell patients.

Hierso R, Waltz X, Mora P, Romana M, Lemonne N, Connes P, Hardy-Dessources MD.

Br J Haematol. 2014 Aug;166(4):601-6. doi: 10.1111/bjh.12912. Epub 2014 Apr 23.

PMID:
24754710
32.

Acute moderate exercise does not further alter the autonomic nervous system activity in patients with sickle cell anemia.

Hedreville M, Charlot K, Waltz X, Sinnapah S, Lemonne N, Etienne-Julan M, Soter V, Hue O, Hardy-Dessources MD, Barthélémy JC, Connes P.

PLoS One. 2014 Apr 16;9(4):e95563. doi: 10.1371/journal.pone.0095563. eCollection 2014.

33.

Association between relative systemic hypertension and otologic disorders in patients with sickle cell-hemoglobin C disorder.

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

Am J Hematol. 2014 Jun;89(6):667. doi: 10.1002/ajh.23717. Epub 2014 Apr 10. No abstract available.

34.

Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease.

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

Haematologica. 2014 May;99(5):74-5. doi: 10.3324/haematol.2014.104745. Epub 2014 Mar 14. No abstract available.

35.

Haemolysis and abnormal haemorheology in sickle cell anaemia.

Connes P, Lamarre Y, Waltz X, Ballas SK, Lemonne N, Etienne-Julan M, Hue O, Hardy-Dessources MD, Romana M.

Br J Haematol. 2014 May;165(4):564-72. doi: 10.1111/bjh.12786. Epub 2014 Feb 24.

PMID:
24611951
36.

Plasma concentration of platelet-derived microparticles is related to painful vaso-occlusive phenotype severity in sickle cell anemia.

Nebor D, Bowers A, Connes P, Hardy-Dessources MD, Knight-Madden J, Cumming V, Reid M, Romana M.

PLoS One. 2014 Jan 24;9(1):e87243. doi: 10.1371/journal.pone.0087243. eCollection 2014.

37.

Decreased hematocrit-to-viscosity ratio and increased lactate dehydrogenase level in patients with sickle cell anemia and recurrent leg ulcers.

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

PLoS One. 2013 Nov 4;8(11):e79680. doi: 10.1371/journal.pone.0079680. eCollection 2013.

38.

Hematological and hemorheological determinants of the six-minute walk test performance in children with sickle cell anemia.

Waltz X, Romana M, Hardy-Dessources MD, Lamarre Y, Divialle-Doumdo L, Petras M, Tarer V, Hierso R, Baltyde KC, Tressières B, Lalanne-Mistrih ML, Maillard F, Hue O, Etienne-Julan M, Connes P.

PLoS One. 2013 Oct 17;8(10):e77830. doi: 10.1371/journal.pone.0077830. eCollection 2013.

39.

Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties.

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

Clin Hemorheol Microcirc. 2014;57(1):63-72. doi: 10.3233/CH-131772.

PMID:
24004554
40.

Male gender, increased blood viscosity, body mass index and triglyceride levels are independently associated with systemic relative hypertension in sickle cell anemia.

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

PLoS One. 2013 Jun 13;8(6):e66004. doi: 10.1371/journal.pone.0066004. Print 2013.

41.

Is there a relationship between the hematocrit-to-viscosity ratio and microvascular oxygenation in brain and muscle?

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

Clin Hemorheol Microcirc. 2015;59(1):37-43. doi: 10.3233/CH-131742.

PMID:
23719422
42.

Natural antiband 3 antibodies in patients with sickle cell disease.

Villaescusa R, Arce AA, Lalanne-Mistrih ML, Lamarre Y, Hierso R, Hernández C, Hardy-Dessources MD; CAREST study group.

C R Biol. 2013 Mar;336(3):173-6. doi: 10.1016/j.crvi.2012.09.002. Epub 2012 Oct 12.

PMID:
23643401
43.

Indirect viscosimetric method is less accurate than ektacytometry for the measurement of red blood cell deformability.

Vent-Schmidt J, Waltz X, Pichon A, Hardy-Dessources MD, Romana M, Connes P.

Clin Hemorheol Microcirc. 2015;59(2):115-21. doi: 10.3233/CH-131727.

PMID:
23594502
44.

Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?

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

Blood. 2013 Apr 11;121(15):3054-6. doi: 10.1182/blood-2013-01-480277. No abstract available.

45.

Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease.

Waltz X, Romana M, Lalanne-Mistrih ML, Machado RF, Lamarre Y, Tarer V, Hardy-Dessources MD, Tressières B, Divialle-Doumdo L, Petras M, Maillard F, Etienne-Julan M, Connes P.

Haematologica. 2013 Jul;98(7):1039-44. doi: 10.3324/haematol.2013.083576. Epub 2013 Mar 28.

46.

Exercise-related complications in sickle cell trait.

Tripette J, Hardy-Dessources MD, Romana M, Hue O, Diaw M, Samb A, Diop S, Connes P.

Clin Hemorheol Microcirc. 2013;55(1):29-37. doi: 10.3233/CH-131687. Review.

PMID:
23478224
47.

Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease.

Lamarre Y, Hardy-Dessources MD, Romana M, Lalanne-Mistrih ML, Waltz X, Petras M, Doumdo L, Blanchet-Deverly A, Martino J, Tressières B, Maillard F, Tarer V, Etienne-Julan M, Connes P.

Clin Hemorheol Microcirc. 2014;58(2):307-16. doi: 10.3233/CH-121661.

48.

Normal muscle oxygen consumption and fatigability in sickle cell patients despite reduced microvascular oxygenation and hemorheological abnormalities.

Waltz X, Pichon A, Lemonne N, Mougenel D, Lalanne-Mistrih ML, Lamarre Y, Tarer V, Tressières B, Etienne-Julan M, Hardy-Dessources MD, Hue O, Connes P.

PLoS One. 2012;7(12):e52471. doi: 10.1371/journal.pone.0052471. Epub 2012 Dec 20.

49.

Hemorheological alterations, decreased cerebral microvascular oxygenation and cerebral vasomotion compensation in sickle cell patients.

Waltz X, Pichon A, Mougenel D, Lemonne N, Lalanne-Mistrih ML, Sinnapah S, Tarer V, Tressières B, Lamarre Y, Etienne-Julan M, Hue O, Hardy-Dessources MD, Connes P.

Am J Hematol. 2012 Dec;87(12):1070-3. doi: 10.1002/ajh.23318. Epub 2012 Aug 22.

50.

Hemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in children with sickle cell disease.

Lamarre Y, Romana M, Waltz X, Lalanne-Mistrih ML, Tressières B, Divialle-Doumdo L, Hardy-Dessources MD, Vent-Schmidt J, Petras M, Broquere C, Maillard F, Tarer V, Etienne-Julan M, Connes P.

Haematologica. 2012 Nov;97(11):1641-7. doi: 10.3324/haematol.2012.066670. Epub 2012 Jun 11.

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