Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 84

1.

Improvement of medical care in a cohort of newborns with sickle-cell disease in North Paris: impact of national guidelines.

Couque N, Girard D, Ducrocq R, Boizeau P, Haouari Z, Missud F, Holvoet L, Ithier G, Belloy M, Odièvre MH, Benemou M, Benhaim P, Retali B, Bensaid P, Monier B, Brousse V, Amira R, Orzechowski C, Lesprit E, Mangyanda L, Garrec N, Elion J, Alberti C, Baruchel A, Benkerrou M.

Br J Haematol. 2016 Jun;173(6):927-37. doi: 10.1111/bjh.14015. Epub 2016 Apr 7.

PMID:
27062606
2.

Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective study.

Benkerrou M, Alberti C, Couque N, Haouari Z, Ba A, Missud F, Boizeau P, Holvoet L, Ithier G, Elion J, Baruchel A, Ducrocq R.

Br J Haematol. 2013 Dec;163(5):646-54. doi: 10.1111/bjh.12590. Epub 2013 Oct 10.

PMID:
24117340
3.

Advantage of HbA1c assay by HPLC D-10 versus cobas integra 400 in a population carrier for HbS and HbC.

Bouzid K, Bahlous A, Ferjani W, Kalai E, Ducrocq R, Ben Mami F, Abdelmoula J.

Clin Lab. 2012;58(7-8):821-8.

PMID:
22997985
4.

Unsuspected glucose-6-phosphate dehydrogenase deficiency presenting as symptomatic methemoglobinemia with severe hemolysis after fava bean ingestion in a 6-year-old boy.

Odièvre MH, Danékova N, Mesples B, Chemouny M, Couque N, Parez N, Ducrocq R, Elion J.

Int J Hematol. 2011 May;93(5):664-666. doi: 10.1007/s12185-011-0827-6. Epub 2011 Apr 12.

PMID:
21479984
5.

[Flowcharts for the diagnosis and the molecular characterization of hemoglobinopathies].

Aguilar-Martinez P, Badens C, Bonello-Palot N, Cadet E, Couque N, Ducrocq R, Elion J, Francina A, Joly P, Pissard S, Rochette J; Réseay DHOS Pathologie héréditaire de l'érythrocyte.

Ann Biol Clin (Paris). 2010 Jul-Aug;68(4):455-64. doi: 10.1684/abc.2010.0457. French.

6.

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
7.

Genetic variants in the noncoding region of RPS19 gene in Diamond-Blackfan anemia: potential implications for phenotypic heterogeneity.

Crétien A, Proust A, Delaunay J, Rincé P, Leblanc T, Ducrocq R, Simansour M, Marie I, Tamary H, Meerpohl J, Niemeyer C, Gazda H, Sieff C, Ball S, Tchernia G, Mohandas N, Da Costa L.

Am J Hematol. 2010 Feb;85(2):111-6. doi: 10.1002/ajh.21601.

8.

[Announcing the diagnosis of sickle cell disease in a newborn to the parents].

Niakaté A, Cavazza F, Perrin A, Brousse V, Bardakdjian J, Ducrocq R, de Montalembert M.

Arch Pediatr. 2009 May;16(5):405-8. doi: 10.1016/j.arcped.2009.02.016. Epub 2009 Mar 24. French. No abstract available.

PMID:
19321324
9.

Neonatal screening for sickle cell disease in France.

Bardakdjian-Michau J, Bahuau M, Hurtrel D, Godart C, Riou J, Mathis M, Goossens M, Badens C, Ducrocq R, Elion J, Perini JM.

J Clin Pathol. 2009 Jan;62(1):31-3. doi: 10.1136/jcp.2008.058867. Erratum in: J Clin Pathol. 2009 Sep;62(9):864. Badens, C [added]; Ducrocq, R [added]; Elion, J [added]; Perini, J M [added].

PMID:
19103855
10.

Effect of transfusion therapy on cerebral vasculopathy in children with sickle-cell anemia.

Bader-Meunier B, Verlhac S, Elmaleh-Bergès M, Ithier G, Sellami F, Faid S, Missud F, Ducrocq R, Alberti C, Zaccaria I, Baruchel A, Benkerrou M.

Haematologica. 2009 Jan;94(1):123-6. doi: 10.3324/haematol.13610. Epub 2008 Dec 4.

11.

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
12.

Molecular basis of alpha-thalassemia in Algeria.

Mesbah-Amroun H, Rouabhi F, Ducrocq R, Elion J.

Hemoglobin. 2008;32(3):273-8. doi: 10.1080/03630260802004301.

PMID:
18473243
13.

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.

14.

The role of the G6PD AEth376G/968C allele in glucose-6-phosphate dehydrogenase deficiency in the seerer population of Senegal.

De Araujo C, Migot-Nabias F, Guitard J, Pelleau S, Vulliamy T, Ducrocq R.

Haematologica. 2006 Feb;91(2):262-3.

15.

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.

16.

Special management of insulin lispro in continuous subcutaneous insulin infusion in young diabetic children: a randomized cross-over study.

Tubiana-Rufi N, Coutant R, Bloch J, Munz-Licha G, Delcroix C, Montaud-Raguideau N, Ducrocq R, Limal JM, Czernichow P.

Horm Res. 2004;62(6):265-71. Epub 2004 Oct 22.

PMID:
15523183
17.

A new high A2-beta-thalassemia due to a 468 bp deletion (-475 to -8) in the beta-globin gene promoter of the intact beta-globin structural gene.

Kueviakoe I, Gerard N, Krishnamoorthy R, Pereira S, Elion J, Ducrocq R.

Hemoglobin. 2004 Feb;28(1):69-72. No abstract available.

PMID:
15008268
18.

Short insertion in a hemoglobin chain: Hb Esch, an unstable alpha1 variant with duplication of the sequence Ala65-Leu-Thr-Asn68.

Préhu C, Groff P, Kalmes G, Golinska B, Riou J, Prome D, Richelme-David S, Kiger L, Ducrocq R, Wajcman H.

Blood Cells Mol Dis. 2003 Sep-Oct;31(2):234-9.

PMID:
12972031
19.

[Good practices for the study of hemoglobin].

Bardakdjian-Michau J, Dhondt JL, Ducrocq R, Galactéros F, Guyard A, Huchet FX, Lahary A, Lena-Russo D, Maboudou P, North ML, Prehu C, Soummer AM, Verschelde M, Wajcman H; Groupe de travail SFBC << Recommandations dans le domaine des diagnostics des hémoglobinopathies >>.

Ann Biol Clin (Paris). 2003 Jul-Aug;61(4):401-9. French. Erratum in: Ann Biol Clin (Paris). 2003 Sep-Oct;61(5):588.

20.

Origin of Hb A2' (Hb B2) [delta16(A13)Gly --> Arg (GGC --> CGC)].

Bennani M, Mombo LE, Chaventre A, Barakat A, Ducrocq R, Nagel RL, Krishnamoorthy R.

Hemoglobin. 2003 May;27(2):105-10.

PMID:
12779272
21.

Foetal haemoglobin in normal healthy adults: relationship with polymorphic sequences cis to the beta globin gene.

Zertal-Zidani S, Ducrocq R, Sahbatou M, Satta D, Krishnamoorthy R.

Eur J Hum Genet. 2002 May;10(5):320-6.

22.

A novel rearrangement of the human fetal globin genes leading to a six gamma-globin gene haplotype.

Gonçalves I, Lavinha J, Ducrocq R, Osório-Almeida L.

Br J Haematol. 2002 Feb;116(2):454-7.

PMID:
11841451
23.

[History of the establishment of pharmacies by mutual benefit societies in Seine-Maritime: the point of view of a dispensary pharmacist].

Ducrocq R.

Rev Hist Pharm (Paris). 2000;48(326):215-20. French. No abstract available.

PMID:
11625748
24.

A novel delta beta fusion gene expresses hemoglobin A (HbA) not Hb Lepore: Senegalese delta(0)beta(+) thalassemia.

Zertal-Zidani S, Ducrocq R, Weil-Olivier C, Elion J, Krishnamoorthy R.

Blood. 2001 Aug 15;98(4):1261-3.

PMID:
11493481
25.

[Neonatal screening for sickle cell anemia: evaluation of a five-year experience in an area of northern Paris].

Ducrocq R, Benkerrou M, Brahimi L, Belloy M, Briard ML, Vilmer E, Elion J.

Arch Pediatr. 2001 May;8(5):474-80. French.

PMID:
11396106
26.

Strategy linking several analytical methods of neonatal screening for sickle cell disease.

Ducrocq R, Pascaud O, Bévier A, Finet C, Benkerrou M, Elion J.

J Med Screen. 2001;8(1):8-14.

PMID:
11373853
27.

[Neonatal screening of sickle cell anemia in metropolitan France].

Bardakjian J, Benkerrou M, Bernaudin F, Briard ML, Ducrocq R, Lambilliotte A, Léna-Russo D, de Montalembert M, Thuret I, Bégué P, Elion J, Galactéros F; Travail du Groupe sur le dépistage néonatal de la drépanocytose.

Arch Pediatr. 2000 Dec;7(12):1261-3. French. No abstract available.

PMID:
11147058
28.

Acute clinical events in 299 homozygous sickle cell patients living in France. French Study Group on Sickle Cell Disease.

Neonato MG, Guilloud-Bataille M, Beauvais P, Bégué P, Belloy M, Benkerrou M, Ducrocq R, Maier-Redelsperger M, de Montalembert M, Quinet B, Elion J, Feingold J, Girot R.

Eur J Haematol. 2000 Sep;65(3):155-64.

PMID:
11007050
29.

Two new Ggamma chain variants: Hb F-clamart [gamma17(A14)Lys-->Asn] and Hb F-Ouled Rabah [gamma19(B1)Asn-->Lys].

Wajcman H, Borensztajn K, Riou J, Promé D, Hurtrel D, Bardakdjian J, Léna-Russo D, Amouroux I, Ducrocq R.

Hemoglobin. 2000 Feb;24(1):45-52.

PMID:
10722115
30.

Evaluation of the Tosoh HLC-723GHb V A1c 2.2 hemoglobin A1c analyzer.

Chevenne D, Marle N, Chauffert M, Noel M, Ducrocq R, Trivin F.

Clin Biochem. 1999 Aug;32(6):487-90. No abstract available.

PMID:
10667488
31.

Spectrum of beta thalassemia mutations and their linkage to beta-globin gene haplotypes in the Indo-Mauritians.

Kotea N, Ramasawmy R, Lu CY, Fa NS, Gerard N, Beesoon S, Ducrocq R, Surrun SK, Nagel RL, Krishnamoorthy R.

Am J Hematol. 2000 Jan;63(1):11-5.

32.

Purification, amplification and characterization of a population of human erythroid progenitors.

Freyssinier JM, Lecoq-Lafon C, Amsellem S, Picard F, Ducrocq R, Mayeux P, Lacombe C, Fichelson S.

Br J Haematol. 1999 Sep;106(4):912-22.

PMID:
10519992
33.

A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobin.

Zertal-Zidani S, Merghoub T, Ducrocq R, Gerard N, Satta D, Krishnamoorthy R.

Hemoglobin. 1999 May;23(2):159-69.

PMID:
10335983
34.

Gamma chain heterogeneity: determination of Hb F composition by perfusion chromatography.

Papassotiriou I, Ducrocq R, Préhu C, Bardakdjian-Michau J, Wajcman H.

Hemoglobin. 1998 Sep-Nov;22(5-6):469-81.

PMID:
9859930
35.

Determination of Hb F levels: the routine methods.

Préhu C, Ducrocq R, Godart C, Riou J, Galactéros F.

Hemoglobin. 1998 Sep-Nov;22(5-6):459-67.

PMID:
9859929
36.

Molecular basis of beta-thalassemia in Bahrain: an epicenter for a Middle East specific mutation.

Jassim N, Merghoub T, Pascaud O, al Mukharraq H, Ducrocq R, Labie D, Elion J, Krishnamoorthy R, Arrayed SA.

Ann N Y Acad Sci. 1998 Jun 30;850:407-9. No abstract available.

PMID:
9668568
37.

New method for quantitative determination of fetal hemoglobin-containing red blood cells by flow cytometry: application to sickle-cell disease.

Navenot JM, Merghoub T, Ducrocq R, Muller JY, Krishnamoorthy R, Blanchard D.

Cytometry. 1998 Jul 1;32(3):186-90.

PMID:
9667507
38.

Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients. The French Study Group on Sickle Cell Disease.

Maier-Redelsperger M, de Montalembert M, Flahault A, Neonato MG, Ducrocq R, Masson MP, Girot R, Elion J.

Blood. 1998 Jun 15;91(12):4472-9.

PMID:
9616141
39.

Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell disease.

Ducrocq R, Bévier A, Leneveu A, Maier-Redelsperger M, Bardakdjian-Michau J, Badens C, Elion J.

J Med Screen. 1998;5(1):27-30.

PMID:
9575456
40.

Combined effect of two different polymorphic sequences within the beta globin gene cluster on the level of HbF.

Gonçalves I, Ducrocq R, Lavinha J, Nogueira PJ, Peres MJ, Picanço I, Correia E Jr, Reis AB, Silva C, Krishnamoorthy R, Almeida LO.

Am J Hematol. 1998 Apr;57(4):269-76.

41.

Uremia and HbA1c measured by high-performance liquid chromatography.

Chevenne D, Fonfrède M, Ducrocq R, Chauffert M, Trivin F.

Diabetes Care. 1998 Mar;21(3):463-4. No abstract available.

PMID:
9540038
42.

Dissection of the association status of two polymorphisms in the beta-globin gene cluster with variations in F-cell number in non-anemic individuals.

Merghoub T, Perichon B, Maier-Redelsperger M, Dibenedetto SP, Samperi P, Ducrocq R, Feingold N, Elion J, Schiliro G, Labie D, Krishnamoorthy R.

Am J Hematol. 1997 Dec;56(4):239-43.

43.

Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell disease.

Helley D, Besmond C, Ducrocq R, da Silva F, Guillin MC, Bezeaud A, Elion J.

Hum Genet. 1997 Aug;100(2):245-8.

PMID:
9254858
44.

Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell Disease.

de Montalembert M, Belloy M, Bernaudin F, Gouraud F, Capdeville R, Mardini R, Philippe N, Jais JP, Bardakdjian J, Ducrocq R, Maier-Redelsperger M, Elion J, Labie D, Girot R.

J Pediatr Hematol Oncol. 1997 Jul-Aug;19(4):313-8.

PMID:
9256830
45.

Effect of alpha-thalassemia on sickle-cell anemia linked to the Arab-Indian haplotype in India.

Mukherjee MB, Lu CY, Ducrocq R, Gangakhedkar RR, Colah RB, Kadam MD, Mohanty D, Nagel RL, Krishnamoorthy R.

Am J Hematol. 1997 Jun;55(2):104-9.

46.

Increased procoagulant activity of red blood cells from patients with homozygous sickle cell disease and beta-thalassemia.

Helley D, Eldor A, Girot R, Ducrocq R, Guillin MC, Bezeaud A.

Thromb Haemost. 1996 Sep;76(3):322-7.

PMID:
8883264
47.

Perfusion chromatography on reversed-phase column allows fast analysis of human globin chains.

Wajcman H, Ducrocq R, Riou J, Mathis M, Godart C, Prehu C, Galacteros F.

Anal Biochem. 1996 May 15;237(1):80-7.

PMID:
8660541
48.

Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals.

Merghoub T, Maier-Redelsperger M, Labie D, Perichon B, Feingold N, Dibenedetto SP, Schiliro G, Samperi P, Ducrocq R, Elion J, Krishnamoorthy R.

Blood. 1996 Mar 15;87(6):2607. No abstract available.

PMID:
8630432
49.
50.

A new alpha chain variant Hb Sallanches [alpha 2 104(G11) Cys-->Tyr] associated with HbH disease in one homozygous patient.

Morlé F, Francina A, Ducrocq R, Wajcman H, Gonnet C, Philippe N, Souillet G, Godet J.

Br J Haematol. 1995 Nov;91(3):608-11.

PMID:
8555062

Supplemental Content

Loading ...
Support Center