Moradkhani K - Search Results

1

Chronic hemolytic anemia due to novel alpha-globin chain variants: critical location of the mutation within the gene sequence for a dominant effect.

Préhu C, Moradkhani K, Riou J, Bahuau M, Launay P, Martin N, Wajcman H, Goossens M, Galactéros F. Préhu C, et al. Among authors: moradkhani k. Haematologica. 2009 Nov;94(11):1624-5. doi: 10.3324/haematol.2009.012971. Epub 2009 Oct 8. Haematologica. 2009. PMID: 19815833 Free PMC article. No abstract available.

2

Hb Gerland [alpha 55(E4)Val-->Ala]: a mutation found on the alpha1-globin gene.

Moradkhani K, Riou J, Francina A, Wajcman H, Prehu C. Moradkhani K, et al. Hemoglobin. 2008;32(5):478-84. doi: 10.1080/03630260802341638. Hemoglobin. 2008. PMID: 18932073

3

Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants.

Moradkhani K, Préhu C, Old J, Henderson S, Balamitsa V, Luo HY, Poon MC, Chui DH, Wajcman H, Patrinos GP. Moradkhani K, et al. Ann Hematol. 2009 Jun;88(6):535-43. doi: 10.1007/s00277-008-0624-3. Epub 2008 Oct 16. Ann Hematol. 2009. PMID: 18923834 Free PMC article.

4

Hb Niigata [beta1(NA1)Val-->Leu] in a Romanian individual resulting from another nucleotide substitution than that found in the Japanese.

Moradkhani K, Henthorn J, Riou J, Phelan L, Préhu C, Wajcman H. Moradkhani K, et al. Hemoglobin. 2007;31(4):477-82. doi: 10.1080/03630260701587885. Hemoglobin. 2007. PMID: 17994382

5

An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) gene.

Moradkhani K, Mazurier E, Giordano PC, Wajcman H, Préhu C. Moradkhani K, et al. Hemoglobin. 2008;32(4):419-24. doi: 10.1080/03630260802173619. Hemoglobin. 2008. PMID: 18654893

6

Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding region.

Ghedira ES, Lecerf L, Faubert E, Costes B, Moradkhani K, Bachir D, Galactéros F, Pissard S. Ghedira ES, et al. Among authors: moradkhani k. Haematologica. 2013 Feb;98(2):305-8. doi: 10.3324/haematol.2012.061994. Epub 2012 Jul 16. Haematologica. 2013. PMID: 22801970 Free PMC article.

7

Pitfalls in the genetic diagnosis of Hb S.

Moradkhani K, Riou J, Wajcman H. Moradkhani K, et al. Clin Biochem. 2013 Mar;46(4-5):291-9. doi: 10.1016/j.clinbiochem.2012.08.018. Epub 2012 Sep 17. Clin Biochem. 2013. PMID: 22995479

8

A rare G6PD variant (c.383T>G; p.128Leu>Arg) with a molecular pathophysiological mechanism similar to that of G6PD A- (68Val>Met, 126Asn>Asp).

Moradkhani K, Bahuau M, Préhu C, Martin N, Bimet C, Galactéros F, Wajcman H. Moradkhani K, et al. Blood Cells Mol Dis. 2009 Nov-Dec;43(3):226-9. doi: 10.1016/j.bcmd.2009.05.007. Epub 2009 Jul 25. Blood Cells Mol Dis. 2009. PMID: 19632868

9

Comparison of two known chromosomal rearrangements in the δβ-globin complex with identical DNA breakpoints but causing different Hb A(2) levels.

Saller E, Moradkhani K, Dutly F, Vinatier I, Préhu C, Frischknecht H, Goossens M. Saller E, et al. Among authors: moradkhani k. Hemoglobin. 2012;36(2):177-82. doi: 10.3109/03630269.2011.644651. Epub 2012 Jan 24. Hemoglobin. 2012. PMID: 22273484 Free article.

10

Disturbance in the HIF-1alpha pathway associated with erythrocytosis: further evidences brought by frameshift and nonsense mutations in the prolyl hydroxylase domain protein 2 (PHD2) gene.

Al-Sheikh M, Moradkhani K, Lopez M, Wajcman H, Préhu C. Al-Sheikh M, et al. Among authors: moradkhani k. Blood Cells Mol Dis. 2008 Mar-Apr;40(2):160-5. doi: 10.1016/j.bcmd.2007.07.017. Epub 2007 Oct 15. Blood Cells Mol Dis. 2008. PMID: 17933562

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