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Items: 15

1.

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.

2.

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.

3.

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.

4.

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.

5.

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
6.

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.

7.

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
8.

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.

9.

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.

10.

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.

11.

Delayed beneficial effect of acute exercise on red blood cell aggregate strength in patients with sickle cell anemia.

Waltz X, Hedreville M, Sinnapah S, Lamarre Y, Soter V, Lemonne N, Etienne-Julan M, Beltan E, Chalabi T, Chout R, Hue O, Mougenel D, Hardy-Dessources MD, Connes P.

Clin Hemorheol Microcirc. 2012;52(1):15-26. doi: 10.3233/CH-2012-1540.

PMID:
22414551
12.

Alpha-thalassemia is associated with a decreased occurrence and a delayed age-at-onset of albuminuria in sickle cell anemia patients.

Nebor D, Broquere C, Brudey K, Mougenel D, Tarer V, Connes P, Elion J, Romana M.

Blood Cells Mol Dis. 2010 Aug 15;45(2):154-8. doi: 10.1016/j.bcmd.2010.06.003. Epub 2010 Jul 3.

PMID:
20598923
13.

Association between Duffy antigen receptor for chemokines expression and levels of inflammation markers in sickle cell anemia patients.

Nebor D, Durpes MC, Mougenel D, Mukisi-Mukaza M, Elion J, Hardy-Dessources MD, Romana M.

Clin Immunol. 2010 Jul;136(1):116-22. doi: 10.1016/j.clim.2010.02.023. Epub 2010 Mar 26.

PMID:
20347396
14.

Effect of interleukin-8 and RANTES on the Gardos channel activity in sickle human red blood cells: role of the Duffy antigen receptor for chemokines.

Durpès MC, Nebor D, du Mesnil PC, Mougenel D, Decastel M, Elion J, Hardy-Dessources MD.

Blood Cells Mol Dis. 2010 Apr 15;44(4):219-23. doi: 10.1016/j.bcmd.2010.02.001. Epub 2010 Mar 2.

PMID:
20199879
15.

Red blood cell aggregation, aggregate strength and oxygen transport potential of blood are abnormal in both homozygous sickle cell anemia and sickle-hemoglobin C disease.

Tripette J, Alexy T, Hardy-Dessources MD, Mougenel D, Beltan E, Chalabi T, Chout R, Etienne-Julan M, Hue O, Meiselman HJ, Connes P.

Haematologica. 2009 Aug;94(8):1060-5. doi: 10.3324/haematol.2008.005371.

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