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Items: 1 to 50 of 233

1.

Evaluation of Outcomes and Quality of Care in Children with Sickle Cell Disease Diagnosed by Newborn Screening: A Real-World Nation-Wide Study in France.

Brousse V, Arnaud C, Lesprit E, Quinet B, Odièvre MH, Etienne-Julan M, Guillaumat C, Elana G, Belloy M, Garnier N, Chamouine A, Dumesnil C, Montalembert M, Pondarre C, Bernaudin F, Couque N, Boutin E, Bardakjian J, Djennaoui F, Ithier G, Benkerrou M, Thuret I.

J Clin Med. 2019 Oct 2;8(10). pii: E1594. doi: 10.3390/jcm8101594.

2.

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.

3.

Implications of a paediatrician-psychologist tandem for sickle cell disease care and impact on cognitive functioning.

Lerner A, Picard H, May A, Gajdos V, Malou-Dhaussy L, Maroja-Cox F, Salomon L, Odièvre MH.

Eur J Pediatr. 2018 Feb;177(2):193-203. doi: 10.1007/s00431-017-3050-5. Epub 2017 Nov 29.

PMID:
29185057
4.

Tuberculosis in children with sickle cell anaemia: a retrospective study in French tertiary care centres.

Droz N, De Lauzanne A, Holvoet L, Missud F, Benkerrou M, Brousse V, Odièvre MH, Faye A, Koehl B.

Eur J Pediatr. 2017 Jun;176(6):723-729. doi: 10.1007/s00431-017-2905-0. Epub 2017 Apr 11.

PMID:
28401342
5.

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
6.

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.

7.

Fetal hemoglobin and hydroxycarbamide moduate both plasma concentration and cellular origin of circulating microparticles in sickle cell anemia children.

Nébor D, Romana M, Santiago R, Vachiery N, Picot J, Broquere C, Chaar V, Doumdo L, Odièvre MH, Benkerrou M, Elion J.

Haematologica. 2013 Jun;98(6):862-7. doi: 10.3324/haematol.2012.073619. Epub 2013 Feb 12.

8.

Acute splenic sequestration crisis in sickle cell disease: cohort study of 190 paediatric patients.

Brousse V, Elie C, Benkerrou M, Odièvre MH, Lesprit E, Bernaudin F, Grimaud M, Guitton C, Quinet B, Dangiolo S, de Montalembert M.

Br J Haematol. 2012 Mar;156(5):643-8. doi: 10.1111/j.1365-2141.2011.08999.x. Epub 2012 Jan 9.

PMID:
22224796
9.

Pathophysiological insights in sickle cell disease.

Odièvre MH, Verger E, Silva-Pinto AC, Elion J.

Indian J Med Res. 2011 Oct;134:532-7. Review.

10.

[Pneumonia due to adenovirus type 7: a case report in a healthy infant].

Odièvre MH, Danékova N, Picard C, Mesples B, BenCheikha Z, Avran D, De Blic J, Leruez-Ville M, Parez N.

Arch Pediatr. 2011 Jul;18(7):772-7. doi: 10.1016/j.arcped.2011.04.005. Epub 2011 May 14. French.

PMID:
21571511
11.

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
12.

[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
13.

[Hypergonadotrophic hypogonadism and congenital galactosemia].

Odièvre MH, Labrune P, Odièvre M.

Arch Pediatr. 2008 Jun;15(6):1124-5. doi: 10.1016/j.arcped.2008.02.006. Epub 2008 Apr 9. French. No abstract available.

PMID:
18400478
14.

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.

15.

[Pneumococcal infection among community-acquired pneumonia. A retrospective study of 230 hospitalized children].

Odièvre MH, Sanni E, de Broucker F, Bonnet E, Michot AS, Laurent C, Valdès L, Weil-Olivier C.

Arch Pediatr. 2007 Nov;14(11):1290-7. Epub 2007 Oct 24. French.

PMID:
17920252
16.

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.

17.

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.

18.

A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of alpha-ketoglutarate dehydrogenase deficiency.

Odièvre MH, Chretien D, Munnich A, Robinson BH, Dumoulin R, Masmoudi S, Kadhom N, Rötig A, Rustin P, Bonnefont JP.

Hum Mutat. 2005 Mar;25(3):323-4. Review.

PMID:
15712224
19.

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
20.

Increased levels of hemostatic proteins are independent of inflammation in glycogen storage disease type Ia.

Marfaing-Koka A, Wolf M, Boyer-Neumann C, Meyer D, Odievre M, Labrune P.

J Pediatr Gastroenterol Nutr. 2003 Nov;37(5):566-70.

PMID:
14581798
21.

[Telephone activity in outpatient pediatric practice].

Assathiany R, Rerolle JM, Messica C, Chevallier B, Odievre M, Arepege.

Arch Pediatr. 2003 Aug;10(8):689-93. French.

PMID:
12922000
22.

[Secondary mitochondrial cytopathy in childhood: a recent concept?].

Odièvre MH, Lombès A, Odièvre M.

Arch Pediatr. 2003 Jun;10(6):497-8. French. No abstract available.

PMID:
12915010
23.

[Archives of Pediatrics 2003: continuity and changes].

Dehan M, Odièvre M.

Arch Pediatr. 2003 Jan;10(1):1. French. No abstract available.

PMID:
12818771
24.

The assessment of IgG avidity in the evaluation of perinatal herpes simplex virus infection.

Odièvre MH, Cointe D, Thébaud B, Zupan V, Ingrand D, Lacaze-Masmonteil T, Grangeot-Keros L.

J Perinatol. 2002 Dec;22(8):669-71.

25.

A secondary respiratory chain defect in a patient with Fanconi-Bickel syndrome.

Odièvre MH, Lombès A, Dessemme P, Santer R, Brivet M, Chevallier B, Lagardère B, Odièvre M.

J Inherit Metab Dis. 2002 Sep;25(5):379-84.

PMID:
12408187
26.

[Nutrition and growth. Synthesis].

Odièvre MH, Olivier C.

Arch Pediatr. 2002 Sep;9 Suppl 4:459s-460s. Review. French. No abstract available.

PMID:
12387166
27.

Long-chain 3-hydroxyacylCoA dehydrogenase deficiency: a new case presenting with liver dysfunction, cholestasis and fibrosis.

Odievre MH, Sevin C, Laurent J, Laboureau JP, Rabier D, Brivet M, Roe C, Wanders RJ, Saudubray JM.

Acta Paediatr. 2002;91(6):719-22.

PMID:
12162610
28.

[Treatment of galactosemia: new strategies?].

Odièvre M.

Arch Pediatr. 2002 Jun;9(6):563-5. French. No abstract available.

PMID:
12108308
29.

[Delay in height-weight growth].

Odièvre MH, Odièvre M.

Rev Prat. 2002 Apr 15;52(8):893-9. French. No abstract available.

PMID:
12053801
30.

[The child as bone marrow donor].

Odièvre M, Michon J.

Arch Pediatr. 2002 Mar;9(3):227-9. French. No abstract available.

PMID:
11938531
31.

[Staphylococcal toxic syndrome, atypical presentation of Kawasaki syndrome or staphylococcal skin syndrome?].

Odièvre MH, Valdès L, Billiard M, Weill C, Michot AS, Olivier C.

Arch Pediatr. 2002 Feb;9(2):155-8. French.

PMID:
11915498
32.

Partial effect of bromocriptine on lactose and galactose synthesis in a pregnant woman heterozygous for galactosaemia.

Odièvre M, Brivet M, Rivière MF, Labrune P.

J Inherit Metab Dis. 2001 Aug;24(4):507-8.

PMID:
11596654
33.

[Reception of parents of hospitalized children].

Odièvre M.

Arch Pediatr. 2001 Jul;8(7):691-3. French. No abstract available.

PMID:
11484449
34.

Methylprednisolone, an alternative to dexamethasone in very premature infants at risk of chronic lung disease.

André P, Thébaud B, Odièvre MH, Razafimahefa H, Zupan V, Dehan M, Lacaze-Masmonteil T.

Intensive Care Med. 2000 Oct;26(10):1496-500.

PMID:
11126262
35.

Genetic heterogeneity of glycogen storage disease type Ia in France: a study of 48 patients.

Trioche P, Francoual J, Chalas J, Capel L, Lindenbaum A, Odièvre M, Labrune P.

Hum Mutat. 2000 Nov;16(5):444.

PMID:
11058903
36.

Azathioprine-induced lung toxicity and efficacy of cyclosporin A in a young girl with type 2 autoimmune hepatitis.

Perreaux F, Zenaty D, Capron F, Trioche P, Odièvre M, Labrune P.

J Pediatr Gastroenterol Nutr. 2000 Aug;31(2):190-2. No abstract available.

PMID:
10941975
37.

Fratries d'enfants atteints de maladie chronique.

Odievre M.

Arch Pediatr. 2000 May;7 Suppl 2:193s. French. No abstract available.

PMID:
10904707
38.

Apolipoprotein E polymorphism and serum concentrations in patients with glycogen storage disease type Ia.

Trioche P, Francoual J, Capel L, Odièvre M, Lindenbaum A, Labrune P.

J Inherit Metab Dis. 2000 Mar;23(2):107-12.

PMID:
10801051
39.

[Prevention of vitamin D deficiency in adolescents and pre-adolescents. An interventional multicenter study on the biological effect of repeated doses of 100,000 IU of vitamin D3].

Duhamel JF, Zeghoud F, Sempé M, Boudailliez B, Odièvre M, Laurans M, Garabédian M, Mallet E.

Arch Pediatr. 2000 Feb;7(2):148-53. French.

PMID:
10701059
40.

[Siblings of children with chronic disease].

Odièvre M.

Arch Pediatr. 1999 Nov;6(11):1149-51. French. No abstract available.

PMID:
10587736
41.

Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene.

Leclerc D, Odièvre M, Wu Q, Wilson A, Huizenga JJ, Rozen R, Scherer SW, Gravel RA.

Gene. 1999 Nov 15;240(1):75-88.

PMID:
10564814
42.

Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndrome.

Trioche P, Chalas J, Francoual J, Capel L, Lindenbaum A, Odièvre M, Labrune P.

Arch Dis Child. 1999 Oct;81(4):301-3.

43.

Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency.

Labrune P, Zittoun J, Duvaltier I, Trioche P, Marquet J, Niaudet P, Odièvre M.

Eur J Pediatr. 1999 Sep;158(9):734-9.

PMID:
10485306
44.

-Headache: an unrecognized risk of ribavirin in infants?

Odièvre M, Gros-Desormeaux A, Jouannault S, Tison M.

Arch Pediatr. 1998 Mar;5(3):347. French. No abstract available.

PMID:
10328015
45.

[A new section: daily pediatrics].

David L, Odièvre M.

Arch Pediatr. 1998 Jan;5(1):1-2. French. No abstract available.

PMID:
10223102
46.

[Skin manifestations of protein glycosylation deficiency, the CDG (carbohydrate deficient glycoprotein) type 1 syndrome].

Vabres P, Sevin C, Amoric JC, Odièvre MH, Saudubray JM, de Prost Y.

Ann Dermatol Venereol. 1998 Oct;125(10):715-6. French.

47.

[Meningitis due to Bacillus cereus in an infant with Reye syndrome].

Ferroni A, Odièvre MH, Abachin E, Révy P, Casanova JL, Saudubray JM, Berche P, Nassif X.

Arch Pediatr. 1998 Oct;5(10):1103-6. French.

PMID:
9809154
48.

Prenatal diagnosis of glycogen storage disease type Ia by restriction enzyme digestion.

Trioche P, Francoual J, Audibert F, Chalas J, Lindenbaum A, Odièvre M, Labrune P.

Prenat Diagn. 1998 Jun;18(6):629-31.

PMID:
9664612
49.

[Vae soli!].

Odièvre M, David L.

Arch Pediatr. 1997 Oct;4(10):935-6. French. No abstract available.

PMID:
9436488
50.

Moyamoya disease in a child with glycogen storage disease type Ia.

Goutières F, Bourgeois M, Trioche P, Demelier JF, Odievre M, Labrune P.

Neuropediatrics. 1997 Apr;28(2):133-4.

PMID:
9208417

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