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Items: 11

1.

Late effects after hematopoietic stem cell transplantation for β-thalassemia major: the French national experience.

Rahal I, Galambrun C, Bertrand Y, Garnier N, Paillard C, Frange P, Pondarré C, Dalle JH, de Latour RP, Michallet M, Steschenko D, Moshous D, Lutz P, Stephan JL, Rohrlich PS, Yakoub-Agha I, Bernaudin F, Piguet C, Aladjidi N, Badens C, Berger C, Socié G, Dumesnil C, Castex MP, Poirée M, Lambilliotte A, Thomas C, Simon P, Auquier P, Michel G, Loundou A, Agouti I, Thuret I.

Haematologica. 2018 Jul;103(7):1143-1149. doi: 10.3324/haematol.2017.183467. Epub 2018 Mar 29.

2.

Platelet and not erythrocyte microparticles are procoagulant in transfused thalassaemia major patients.

Agouti I, Cointe S, Robert S, Judicone C, Loundou A, Driss F, Brisson A, Steschenko D, Rose C, Pondarré C, Bernit E, Badens C, Dignat-George F, Lacroix R, Thuret I.

Br J Haematol. 2015 Nov;171(4):615-24. doi: 10.1111/bjh.13609. Epub 2015 Jul 24.

PMID:
26205481
3.

Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome.

Lacoste C, Leheup B, Agouti I, Mowat D, Giuliano F, Badens C.

Clin Genet. 2014 Nov;86(5):502-3. doi: 10.1111/cge.12319. Epub 2013 Dec 1. No abstract available.

PMID:
24289169
4.

Analytical evaluation of the Capillarys 2 Flex piercing for routine haemoglobinopathies diagnosis.

Agouti I, Merono F, Bonello-Palot N, Badens C.

Int J Lab Hematol. 2013 Apr;35(2):217-21. doi: 10.1111/ijlh.12000. Epub 2012 Sep 4.

PMID:
22943067
5.

Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the disease.

Badens C, Joly P, Agouti I, Thuret I, Gonnet K, Fattoum S, Francina A, Simeoni MC, Loundou A, Pissard S.

Haematologica. 2011 Nov;96(11):1712-4. doi: 10.3324/haematol.2011.046748. Epub 2011 Jul 26.

6.

Analytical evaluation of the Tosoh HLC-723 G8 automated HPLC analyzer for hemoglobin analysis in beta-thalassemia mode.

Merono F, Agouti I, Bonello-Palot N, Paolasso C, Levy N, Badens C.

Clin Biochem. 2011 Apr;44(5-6):441-3. doi: 10.1016/j.clinbiochem.2010.12.007. Epub 2010 Dec 28.

PMID:
21192923
7.

The rare codon 24 (T>A) (beta+) mutation in association with the common codon 39 (C> T) (beta0) mutation causes transfusion-dependent beta-thalassemia in a Moroccan patient.

Agouti I, Bennani M, Levy N, Giordano P, Badens C.

Hemoglobin. 2009;33(2):150-4. doi: 10.1080/03630260902861998.

PMID:
19373592
8.

Molecular basis of beta-thalassemia in Morocco: possible origins of the molecular heterogeneity.

Agouti I, Badens C, Abouyoub A, Levy N, Bennani M.

Genet Test. 2008 Dec;12(4):563-8. doi: 10.1089/gte.2008.0058.

PMID:
18976160
9.

Beta-thalassemia intermedia due to two novel mutations in the promoter region of the beta-globin gene.

Agouti I, Bennani M, Nezri M, Levy N, Badens C.

Eur J Haematol. 2008 Apr;80(4):346-50. Epub 2007 Dec 10.

PMID:
18081706
10.

Thalassemia intermedia due to a novel mutation in the second intervening sequence of the beta-globin gene.

Agouti I, Bennani M, Ahmed A, Barakat A, Mohamed K, Badens C.

Hemoglobin. 2007;31(4):433-8.

PMID:
17994377
11.

Genotypic correlation between six common beta-thalassemia mutations and the XmnI polymorphism in the Moroccan population.

Agouti I, Badens C, Abouyoub A, Khattab M, Sayah F, Barakat A, Bennani M.

Hemoglobin. 2007;31(2):141-9.

PMID:
17486495

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