Levy N - Search Results

1

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. Among authors: levy n. 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

2

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. Among authors: levy n. Genet Test. 2008 Dec;12(4):563-8. doi: 10.1089/gte.2008.0058. Genet Test. 2008. PMID: 18976160

3

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. Among authors: levy n. Hemoglobin. 2009;33(2):150-4. doi: 10.1080/03630260902861998. Hemoglobin. 2009. PMID: 19373592

4

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: levy n. 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

5

[ATR-X syndrome: a new mutation in the XNP/ATRX gene near the helicase domain].

Giuliano F, Badens C, Richelme C, Levy N, Lambert JC. Giuliano F, et al. Among authors: levy n. Arch Pediatr. 2005 Sep;12(9):1372-5. doi: 10.1016/j.arcped.2005.03.053. Arch Pediatr. 2005. PMID: 16125058 French.

6

ATRX syndrome in a girl with a heterozygous mutation in the ATRX Zn finger domain and a totally skewed X-inactivation pattern.

Badens C, Martini N, Courrier S, DesPortes V, Touraine R, Levy N, Edery P. Badens C, et al. Among authors: levy n. Am J Med Genet A. 2006 Oct 15;140(20):2212-5. doi: 10.1002/ajmg.a.31400. Am J Med Genet A. 2006. PMID: 16955409

7

First case of gamma-thalassemia in association with a betaS allele: a pitfall in the neonatal screening for sickle cell disease.

Lacoste C, Bonello-Palot N, Gonnet K, Merono F, Levy N, Thuret I, Badens C. Lacoste C, et al. Among authors: levy n. Haematologica. 2008 Nov;93(11):1754-5. doi: 10.3324/haematol.13262. Epub 2008 Aug 25. Haematologica. 2008. PMID: 18728021 Free article. No abstract available.

8

Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome.

Badens C, Lacoste C, Philip N, Martini N, Courrier S, Giuliano F, Verloes A, Munnich A, Leheup B, Burglen L, Odent S, Van Esch H, Levy N. Badens C, et al. Among authors: levy n. Clin Genet. 2006 Jul;70(1):57-62. doi: 10.1111/j.1399-0004.2006.00641.x. Clin Genet. 2006. PMID: 16813605

9

Novel mutations in TTC37 associated with tricho-hepato-enteric syndrome.

Fabre A, Martinez-Vinson C, Roquelaure B, Missirian C, André N, Breton A, Lachaux A, Odul E, Colomb V, Lemale J, Cézard JP, Goulet O, Sarles J, Levy N, Badens C. Fabre A, et al. Among authors: levy n. Hum Mutat. 2011 Mar;32(3):277-81. doi: 10.1002/humu.21420. Epub 2011 Feb 17. Hum Mutat. 2011. PMID: 21120949

10

A Rare Mutation in LMNB2 Associated with Lipodystrophy Drives Premature Cell Senescence.

Varlet AA, Desgrouas C, Jebane C, Bonello-Palot N, Bourgeois P, Levy N, Helfer E, Dubois N, Valero R, Badens C, Beliard S. Varlet AA, et al. Among authors: levy n. Cells. 2021 Dec 24;11(1):50. doi: 10.3390/cells11010050. Cells. 2021. PMID: 35011612 Free PMC article.

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