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Increased retention of functional mitochondria in mature sickle red blood cells is associated with increased sickling tendency, hemolysis and oxidative stress.
Esperti S, Nader E, Stier A, Boisson C, Carin R, Marano M, Robert M, Martin M, Horand F, Cibiel A, Renoux C, Van Bruggen R, Blans C, Dargaud Y, Joly P, Gauthier A, Poutrel S, Romana M, Roussel D, Connes P. Esperti S, et al. Among authors: connes p. Haematologica. 2023 Nov 1;108(11):3086-3094. doi: 10.3324/haematol.2023.282684. Haematologica. 2023. PMID: 37259576 Free PMC article.
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. Tripette J, et al. Among authors: connes p. Haematologica. 2009 Aug;94(8):1060-5. doi: 10.3324/haematol.2008.005371. Haematologica. 2009. PMID: 19644138 Free PMC article.
Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation.
Nebor D, Bowers A, Hardy-Dessources MD, Knight-Madden J, Romana M, Reid H, Barthélémy JC, Cumming V, Hue O, Elion J, Reid M, Connes P; CAREST Study Group. Nebor D, et al. Among authors: connes p. Haematologica. 2011 Nov;96(11):1589-94. doi: 10.3324/haematol.2011.047365. Epub 2011 Jul 12. Haematologica. 2011. PMID: 21750084 Free PMC article. Clinical Trial.
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. Lamarre Y, et al. Among authors: connes p. Haematologica. 2012 Nov;97(11):1641-7. doi: 10.3324/haematol.2012.066670. Epub 2012 Jun 11. Haematologica. 2012. PMID: 22689686 Free PMC article. Clinical Trial.
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. Lamarre Y, et al. Among authors: connes p. Clin Hemorheol Microcirc. 2014;58(2):307-16. doi: 10.3233/CH-121661. Clin Hemorheol Microcirc. 2014. PMID: 23302597 Free PMC article.
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. Waltz X, et al. Among authors: connes p. Haematologica. 2013 Jul;98(7):1039-44. doi: 10.3324/haematol.2013.083576. Epub 2013 Mar 28. Haematologica. 2013. PMID: 23539539 Free PMC article.
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. Lamarre Y, et al. Among authors: connes p. PLoS One. 2013 Jun 13;8(6):e66004. doi: 10.1371/journal.pone.0066004. Print 2013. PLoS One. 2013. PMID: 23785465 Free PMC article.
292 results