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Items: 1 to 50 of 64

1.

Insights into determinants of spleen injury in sickle cell anemia.

El Hoss S, Cochet S, Marin M, Lapouméroulie C, Dussiot M, Bouazza N, Elie C, de Montalembert M, Arnaud C, Guitton C, Pellegrino B, Odièvre MH, Moati F, Le Van Kim C, Aronovicz YC, El Nemer W, Brousse V.

Blood Adv. 2019 Aug 13;3(15):2328-2336. doi: 10.1182/bloodadvances.2019000106.

2.

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
3.

Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference.

Lobitz S, Telfer P, Cela E, Allaf B, Angastiniotis M, Backman Johansson C, Badens C, Bento C, Bouva MJ, Canatan D, Charlton M, Coppinger C, Daniel Y, de Montalembert M, Ducoroy P, Dulin E, Fingerhut R, Frömmel C, García-Morin M, Gulbis B, Holtkamp U, Inusa B, James J, Kleanthous M, Klein J, Kunz JB, Langabeer L, Lapouméroulie C, Marcao A, Marín Soria JL, McMahon C, Ohene-Frempong K, Périni JM, Piel FB, Russo G, Sainati L, Schmugge M, Streetly A, Tshilolo L, Turner C, Venturelli D, Vilarinho L, Yahyaoui R, Elion J, Colombatti R; with the endorsement of EuroBloodNet, the European Reference Network in Rare Haematological Diseases.

Br J Haematol. 2018 Nov;183(4):648-660. doi: 10.1111/bjh.15600. Epub 2018 Oct 18.

PMID:
30334577
4.

A microfluidic approach to study the effect of mechanical stress on erythrocytes in sickle cell disease.

Lizarralde Iragorri MA, El Hoss S, Brousse V, Lefevre SD, Dussiot M, Xu T, Ferreira AR, Lamarre Y, Silva Pinto AC, Kashima S, Lapouméroulie C, Covas DT, Le Van Kim C, Colin Y, Elion J, Français O, Le Pioufle B, El Nemer W.

Lab Chip. 2018 Sep 26;18(19):2975-2984. doi: 10.1039/c8lc00637g.

PMID:
30168832
5.

Prognostic factors of disease severity in infants with sickle cell anemia: A comprehensive longitudinal cohort study.

Brousse V, El Hoss S, Bouazza N, Arnaud C, Bernaudin F, Pellegrino B, Guitton C, Odièvre-Montanié MH, Mames D, Brouzes C, Picard V, Nguyen-Khoa T, Pereira C, Lapouméroulie C, Pissard S, Gardner K, Menzel S, Le Van Kim C, Colin-Aronovicz Y, Buffet P, Mohandas N, Elie C, Maier-Redelsperger M, El Nemer W, de Montalembert M.

Am J Hematol. 2018 Nov;93(11):1411-1419. doi: 10.1002/ajh.25260. Epub 2018 Sep 21.

PMID:
30132969
6.

Effects of Poloxamer 188 on red blood cell membrane properties in sickle cell anaemia.

Sandor B, Marin M, Lapoumeroulie C, Rabaï M, Lefevre SD, Lemonne N, El Nemer W, Mozar A, Français O, Le Pioufle B, Connes P, Le Van Kim C.

Br J Haematol. 2016 Apr;173(1):145-9. doi: 10.1111/bjh.13937. Epub 2016 Feb 5.

PMID:
26846309
7.

Erythroid Adhesion Molecules in Sickle Cell Anaemia Infants: Insights Into Early Pathophysiology.

Brousse V, Colin Y, Pereira C, Arnaud C, Odièvre MH, Boutemy A, Guitton C, de Montalembert M, Lapouméroulie C, Picot J, Le Van Kim C, El Nemer W.

EBioMedicine. 2014 Dec 18;2(2):154-7. doi: 10.1016/j.ebiom.2014.12.006. eCollection 2015.

8.

Hydroxycarbamide decreases sickle reticulocyte adhesion to resting endothelium by inhibiting endothelial lutheran/basal cell adhesion molecule (Lu/BCAM) through phosphodiesterase 4A activation.

Chaar V, Laurance S, Lapoumeroulie C, Cochet S, De Grandis M, Colin Y, Elion J, Le Van Kim C, El Nemer W.

J Biol Chem. 2014 Apr 18;289(16):11512-21. doi: 10.1074/jbc.M113.506121. Epub 2014 Mar 10.

9.

Clinical and molecular findings of chronic granulomatous disease in Oman: family studies.

Al-Zadjali S, Al-Tamemi S, Elnour I, AlKindi S, Lapoumeroulie C, Al-Maamari S, Pathare A, Dennison D, Krishnamoorthy R.

Clin Genet. 2015 Feb;87(2):185-9. doi: 10.1111/cge.12351. Epub 2014 Feb 17.

PMID:
24446915
10.

Prior exposure of endothelial cells to hydroxycarbamide alters the flow dynamics and adhesion of sickle red blood cells.

Verger E, Schoëvaërt D, Carrivain P, Victor JM, Lapouméroulie C, Elion J.

Clin Hemorheol Microcirc. 2014;57(1):9-22. doi: 10.3233/CH-131762.

PMID:
24002118
11.

A stepwise α-thalassemia screening strategy in high-prevalence areas.

Alkindi SS, Alzadjali S, Daar S, Sindhuvi E, Wali Y, Pathare AV, Venugopal S, Lapoumeroulie C, Srivastava A, Krishnamoorthy R.

Eur J Haematol. 2013 Aug;91(2):164-9. doi: 10.1111/ejh.12136. Epub 2013 Jun 15.

PMID:
23668236
12.

Warfarin pharmacogenetics: development of a dosing algorithm for Omani patients.

Pathare A, Al Khabori M, Alkindi S, Al Zadjali S, Misquith R, Khan H, Lapoumeroulie C, Paldi A, Krishnamoorthy R.

J Hum Genet. 2012 Oct;57(10):665-9. doi: 10.1038/jhg.2012.94. Epub 2012 Aug 2.

PMID:
22854539
13.

Warfarin pharmacogenetics: polymorphisms of the CYP2C9, CYP4F2, and VKORC1 loci in a genetically admixed Omani population.

Pathare AV, Al Zadjali S, Misquith R, Alkindi SS, Panjwani V, Lapoumeroulie C, Pravin S, Paldi A, Krishnamoorthy R.

Hum Biol. 2012 Feb;84(1):67-77. doi: 10.3378/027.084.0103.

PMID:
22452429
14.

[Pathophysiology of sickle cell disease].

Elion J, Laurance S, Lapouméroulie C.

Med Trop (Mars). 2010 Dec;70(5-6):454-8. Review. French.

PMID:
21520646
15.

Differential modulation of adhesion molecule expression by hydroxycarbamide in human endothelial cells from the micro- and macrocirculation: potential implications in sickle cell disease vasoocclusive events.

Laurance S, Lansiaux P, Pellay FX, Hauchecorne M, Benecke A, Elion J, Lapoumeroulie C.

Haematologica. 2011 Apr;96(4):534-42. doi: 10.3324/haematol.2010.026740. Epub 2011 Jan 12.

16.

Variants of the mannose-binding lectin gene in the Benin population: heterozygosity for the p.G57E allele may confer a selective advantage. 2007.

Dossou-Yovo OP, Lapoumeroulie C, Hauchecorne M, Zaccaria I, Ducrocq R, Krishnamoorthy R, Rahimy MC, Elion J.

Hum Biol. 2009 Dec;81(5-6):899-909. doi: 10.3378/027.081.0630.

PMID:
20504205
17.

Hydroxycarbamide stimulates the production of proinflammatory cytokines by endothelial cells: relevance to sickle cell disease.

Laurance S, Pellay FX, Dossou-Yovo OP, Verger E, Krishnamoorthy R, Lapoumeroulie C, Benecke A, Elion J.

Pharmacogenet Genomics. 2010 Apr;20(4):257-68. doi: 10.1097/FPC.0b013e32833854d6.

PMID:
20216336
18.

Effects of RANTES and MBL2 gene polymorphisms in sickle cell disease clinical outcomes: association of the g.In1.1T>C RANTES variant with protection against infections.

Dossou-Yovo OP, Zaccaria I, Benkerrou M, Hauchecorne M, Alberti C, Rahimy MC, Elion J, Lapoumeroulie C.

Am J Hematol. 2009 Jun;84(6):378-80. doi: 10.1002/ajh.21411. No abstract available.

19.

[Effect of hydroxyurea on adhesion proteins in sickle cell anemia].

Odièvre MH, Lapouméroulie C, Elion J.

Arch Pediatr. 2009 Feb;16(2):95-8. doi: 10.1016/j.arcped.2008.11.003. Epub 2009 Jan 23. French. No abstract available.

PMID:
19167870
20.

Variants of the mannose-binding lectin gene in the Benin population: heterozygosity for the p.G57E allele may confer a selective advantage.

Dossou-Yovo OP, Lapoumeroulie C, Hauchecorne M, Zaccaria I, Ducrocq R, Krishnamoorthy R, Rahimy MC, Elion J.

Hum Biol. 2007 Dec;79(6):687-97.

PMID:
18494378
21.

Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease.

Odièvre MH, Bony V, Benkerrou M, Lapouméroulie C, Alberti C, Ducrocq R, Jacqz-Aigrain E, Elion J, Cartron JP.

Haematologica. 2008 Apr;93(4):502-10. doi: 10.3324/haematol.12070. Epub 2008 Mar 5. Erratum in: Haematologica. 2009 Apr;94(4):598.

22.

Endothelial cells do not express GSTA1: potential relevance to busulfan-mediated endothelial damage during haematopoietic stem cell transplantation.

Vassord C, Lapouméroulie C, Koumaravelou K, Srivastava A, Krishnamoorthy R.

Eur J Haematol. 2008 Apr;80(4):299-302. doi: 10.1111/j.1600-0609.2008.01031.x. Epub 2008 Jan 14.

PMID:
18194479
23.

Sodium phenyl butyrate downregulates endothelin-1 expression in cultured human endothelial cells: relevance to sickle-cell disease.

Odièvre MH, Brun M, Krishnamoorthy R, Lapouméroulie C, Elion J.

Am J Hematol. 2007 May;82(5):357-62.

24.

Decreased plasma endothelin-1 levels in children with sickle cell disease treated with hydroxyurea.

Lapouméroulie C, Benkerrou M, Odièvre MH, Ducrocq R, Brun M, Elion J.

Haematologica. 2005 Mar;90(3):401-3.

25.

Vaso-occlusion in sickle cell anemia: role of interactions between blood cells and endothelium.

Elion JE, Brun M, Odièvre MH, Lapouméroulie CL, Krishnamoorthy R.

Hematol J. 2004;5 Suppl 3:S195-8. Review. No abstract available.

PMID:
15190308
26.

Hydroxyurea downregulates endothelin-1 gene expression and upregulates ICAM-1 gene expression in cultured human endothelial cells.

Brun M, Bourdoulous S, Couraud PO, Elion J, Krishnamoorthy R, Lapoumeroulie C.

Pharmacogenomics J. 2003;3(4):215-26.

PMID:
12931135
27.

Mannose-binding lectin alleles in sub-Saharan Africans and relation with susceptibility to infections.

Mombo LE, Lu CY, Ossari S, Bedjabaga I, Sica L, Krishnamoorthy R, Lapoumeroulie C.

Genes Immun. 2003 Jul;4(5):362-7.

PMID:
12847552
28.

A novel mechanism for thalassaemia intermedia.

Badens C, Mattei MG, Imbert AM, Lapouméroulie C, Martini N, Michel G, Lena-Russo D.

Lancet. 2002 Jan 12;359(9301):132-3.

PMID:
11809258
29.

Anthropogenetical analysis of abnormal human alpha-globin gene cluster arrangement on chromosome 16.

Turcinov D, Krishnamoorthy R, Janićijević B, Marković I, Mustać M, Lapoumeroulie C, Chaventré A, Rudan P.

Coll Antropol. 2000 Dec;24(2):295-301.

PMID:
11216396
30.

Atypical beta(s) haplotypes are generated by diverse genetic mechanisms.

Zago MA, Silva WA Jr, Dalle B, Gualandro S, Hutz MH, Lapoumeroulie C, Tavella MH, Araujo AG, Krieger JE, Elion J, Krishnamoorthy R.

Am J Hematol. 2000 Feb;63(2):79-84.

31.

Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections.

Neonato MG, Lu CY, Guilloud-Bataille M, Lapouméroulie C, Nabeel-Jassim H, Dabit D, Girot R, Krishnamoorthy R, Feingold J, Besmond C, Elion J.

Eur J Hum Genet. 1999 Sep;7(6):679-86.

32.

Genetic variations in human fetal globin gene microsatellites and their functional relevance.

Lapoumeroulie C, Castiglia L, Ruberto C, Fichera M, Amata S, Labie D, Ragusa A.

Hum Genet. 1999 Apr;104(4):307-14.

PMID:
10369160
33.

CFTR regions containing duodenum specific DNase I hypersensitive sites drive expression in intestinal crypt cells but not in fibroblasts.

Dixméras I, Lapouméroulie C, Tallec LP, Bens M, Elion J, Vandewalle A, Denamur E.

Biochem Biophys Res Commun. 1998 Sep 18;250(2):328-34.

PMID:
9753629
34.

Cross-species characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene reveals multiple levels of regulation.

Vuillaumier S, Dixmeras I, Messaï H, Lapouméroulie C, Lallemand D, Gekas J, Chehab FF, Perret C, Elion J, Denamur E.

Biochem J. 1997 Nov 1;327 ( Pt 3):651-62.

35.

Haemoglobin D-Ouled Rabah among the Mozabites: a relevant variant to trace the origin of Berber-speaking populations.

Merghoub T, Sanchez-Mazas A, Tamouza R, Lu CY, Bouzid K, Ardjoun FZ, Labie D, Lapouméroulie C, Elion J.

Eur J Hum Genet. 1997 Nov-Dec;5(6):390-6.

PMID:
9450184
36.

Molecular basis of alpha-thalassemia in Sicily.

Fichera M, Spalletta A, Fiorenza F, Lombardo T, Schilirò G, Tamouza R, Lapouméroulie C, Labie D, Ragusa A.

Hum Genet. 1997 Mar;99(3):381-6.

PMID:
9050927
37.

Resistance to HIV-1 infection in caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene.

Samson M, Libert F, Doranz BJ, Rucker J, Liesnard C, Farber CM, Saragosti S, Lapoumeroulie C, Cognaux J, Forceille C, Muyldermans G, Verhofstede C, Burtonboy G, Georges M, Imai T, Rana S, Yi Y, Smyth RJ, Collman RG, Doms RW, Vassart G, Parmentier M.

Nature. 1996 Aug 22;382(6593):722-5.

PMID:
8751444
38.

Transcriptional regulation of rat alpha 1-acid glycoprotein gene by phenobarbital.

Fournier T, Mejdoubi N, Lapoumeroulie C, Hamelin J, Elion J, Durand G, Porquet D.

J Biol Chem. 1994 Nov 4;269(44):27175-8.

39.

Nucleotide sequences of the genes coding for the TEM-like beta-lactamases IRT-1 and IRT-2 (formerly called TRI-1 and TRI-2).

Belaaouaj A, Lapoumeroulie C, Caniça MM, Vedel G, Névot P, Krishnamoorthy R, Paul G.

FEMS Microbiol Lett. 1994 Jul 1;120(1-2):75-80.

PMID:
8056297
40.
41.

Inter-ethnic polymorphism of the beta-globin gene locus control region (LCR) in sickle-cell anemia patients.

Périchon B, Ragusa A, Lapouméroulie C, Romand A, Moi P, Ikuta T, Labie D, Elion J, Krishnamoorthy R.

Hum Genet. 1993 Jun;91(5):464-8.

PMID:
8314558
42.

Molecular pathology of beta thalassemia intermedia.

Lu CY, Ragusa A, Goncalves I, Lapoumeroulie C, Krishnamoorthy R.

Nouv Rev Fr Hematol. 1993 Jun;35(3):317-8. No abstract available.

PMID:
7687777
43.

Analysis of the 5' flanking sequence of the G gamma globin gene by denaturing gradient gel electrophoresis confirms the heterogeneity of the Bantu beta S haplotype.

Tachdjian G, Benabdennebi M, Guidal C, Sayada C, Lapouméroulie C, Elion J.

Hum Genet. 1992 Sep-Oct;90(1-2):23-6.

PMID:
1358788
44.

A haplotype-linked four base pair deletion upstream of the A gamma globin gene coincides with decreased gene expression.

Beldjord C, Ducrocq R, Nadifi S, Lapoumeroulie C, Elion J, Labie D.

Hum Genet. 1992 Aug;89(6):625-8.

PMID:
1355067
45.

A novel sickle cell mutation of yet another origin in Africa: the Cameroon type.

Lapouméroulie C, Dunda O, Ducrocq R, Trabuchet G, Mony-Lobé M, Bodo JM, Carnevale P, Labie D, Elion J, Krishnamoorthy R.

Hum Genet. 1992 May;89(3):333-7.

PMID:
1376298
46.

DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation.

Elion J, Berg PE, Lapouméroulie C, Trabuchet G, Mittelman M, Krishnamoorthy R, Schechter AN, Labie D.

Blood. 1992 Feb 1;79(3):787-92.

47.

Nucleotide sequence evidence of the unicentric origin of the beta C mutation in Africa.

Trabuchet G, Elion J, Dunda O, Lapouméroulie C, Ducrocq R, Nadifi S, Zohoun I, Chaventre A, Carnevale P, Nagel RL, et al.

Hum Genet. 1991 Sep;87(5):597-601.

PMID:
1680789
48.

Haplotypes in tribal Indians bearing the sickle gene: evidence for the unicentric origin of the beta S mutation and the unicentric origin of the tribal populations of India.

Labie D, Srinivas R, Dunda O, Dode C, Lapoumeroulie C, Devi V, Devi S, Ramasami K, Elion J, Ducrocq R, et al.

Hum Biol. 1989 Aug;61(4):479-91.

PMID:
2480325
49.

[Intermediate homozygous beta-thalassemia with high fetal hemoglobin synthesis. Molecular analysis].

Cohen-Haguenauer O, Lapoumeroulie C, Labie D, Girot R.

Presse Med. 1989 Feb 4;18(4):173-6. French.

PMID:
2466287
50.

DNA haplotype distribution in Algerian beta thalassaemia patients. An extended evaluation by family studies and representative molecular characterization.

Rouabhi F, Lapouméroulie C, Amselem S, Krishnamoorthy R, Adjrad L, Girot R, Chardin P, Benabdji M, Labie D, Beldjord C.

Hum Genet. 1988 Aug;79(4):373-6.

PMID:
2900801

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