Agouti I - Search Results

1

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. Agouti I, et al. Hemoglobin. 2007;31(4):433-8. doi: 10.1080/03630260701613210. Hemoglobin. 2007. PMID: 17994377

2

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. Agouti I, et al. Hemoglobin. 2007;31(2):141-9. doi: 10.1080/03630260701285050. Hemoglobin. 2007. PMID: 17486495

3

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. Agouti I, et al. Eur J Haematol. 2008 Apr;80(4):346-50. doi: 10.1111/j.1600-0609.2007.01017.x. Epub 2007 Dec 10. Eur J Haematol. 2008. PMID: 18081706

4

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

Agouti I, Badens C, Abouyoub A, Levy N, Bennani M. Agouti I, et al. Genet Test. 2008 Dec;12(4):563-8. doi: 10.1089/gte.2008.0058. Genet Test. 2008. PMID: 18976160

5

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. Agouti I, et al. Hemoglobin. 2009;33(2):150-4. doi: 10.1080/03630260902861998. Hemoglobin. 2009. PMID: 19373592

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. Merono F, et al. Among authors: agouti i. Clin Biochem. 2011 Apr;44(5-6):441-3. doi: 10.1016/j.clinbiochem.2010.12.007. Epub 2010 Dec 28. Clin Biochem. 2011. PMID: 21192923

7

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. Badens C, et al. Among authors: agouti i. Haematologica. 2011 Nov;96(11):1712-4. doi: 10.3324/haematol.2011.046748. Epub 2011 Jul 26. Haematologica. 2011. PMID: 21791466 Free PMC article. Clinical Trial.

8

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

Agouti I, Merono F, Bonello-Palot N, Badens C. Agouti I, et al. Int J Lab Hematol. 2013 Apr;35(2):217-21. doi: 10.1111/ijlh.12000. Epub 2012 Sep 4. Int J Lab Hematol. 2013. PMID: 22943067

9

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. Lacoste C, et al. Among authors: agouti i. Clin Genet. 2014 Nov;86(5):502-3. doi: 10.1111/cge.12319. Epub 2013 Dec 1. Clin Genet. 2014. PMID: 24289169 No abstract available.

10

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. Agouti I, et al. Br J Haematol. 2015 Nov;171(4):615-24. doi: 10.1111/bjh.13609. Epub 2015 Jul 24. Br J Haematol. 2015. PMID: 26205481 Free article.

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