Gerard N - Search Results

1

A novel beta-thalassemia mutation in an Asian Indian.

Shaji RV, Gerard N, Krishnamoorthy R, Srivastava A, Chandy M. Shaji RV, et al. Among authors: gerard n. Hemoglobin. 2002 Feb;26(1):49-57. doi: 10.1081/hem-120002940. Hemoglobin. 2002. PMID: 11939512

2

A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene (GAG-->TAG) in a Tunisian family.

Siala H, Fattoum S, Messaoud T, Ouali F, Gerard N, Krishnamoorthy R. Siala H, et al. Among authors: gerard n. Hemoglobin. 2004 Aug;28(3):249-54. doi: 10.1081/hem-120040258. Hemoglobin. 2004. PMID: 15481894

3

A new high A2-beta-thalassemia due to a 468 bp deletion (-475 to -8) in the beta-globin gene promoter of the intact beta-globin structural gene.

Kueviakoe I, Gerard N, Krishnamoorthy R, Pereira S, Elion J, Ducrocq R. Kueviakoe I, et al. Among authors: gerard n. Hemoglobin. 2004 Feb;28(1):69-72. doi: 10.1081/hem-120028890. Hemoglobin. 2004. PMID: 15008268 No abstract available.

4

Molecular basis of thalassemia in Qatar.

Al-Obaidli A, Hamodat M, Fawzi Z, Abu-Laban M, Gerard N, Krishnamoorthy R. Al-Obaidli A, et al. Among authors: gerard n. Hemoglobin. 2007;31(2):121-7. doi: 10.1080/03630260701288815. Hemoglobin. 2007. PMID: 17486492

5

A novel deletional beta-thalassemic variant in an ethnic Qatari patient.

Al-Obaidli A, Gerard N, Al Zadjali S, Fawzi Z, Pravin S, Pathare A, Krishnamoorthy R. Al-Obaidli A, et al. Among authors: gerard n. Hemoglobin. 2009;33(3):214-9. doi: 10.1080/03630260903081398. Hemoglobin. 2009. PMID: 19657835

6

Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.

Bravo-Urquiola M, Arends A, Gómez G, Montilla S, Gerard N, Chacin M, Berbar T, García O, García G, Velasquez D, Castillo O, Krishnamoorthy R. Bravo-Urquiola M, et al. Among authors: gerard n. Hemoglobin. 2012;36(3):209-18. doi: 10.3109/03630269.2012.674997. Hemoglobin. 2012. PMID: 22563936

7

A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobin.

Zertal-Zidani S, Merghoub T, Ducrocq R, Gerard N, Satta D, Krishnamoorthy R. Zertal-Zidani S, et al. Among authors: gerard n. Hemoglobin. 1999 May;23(2):159-69. doi: 10.3109/03630269908996160. Hemoglobin. 1999. PMID: 10335983

8

A mismatched-primer polymerase chain reaction-restriction fragment length polymorphism strategy for rapid screening of the polyadenylation signal mutation alpha(T-Saudi) (AATAAA-->AATAAG) in the alpha2-globin gene.

Jassim N, Al-Arrayed S, Gerard N, Al-Mukharraq H, Al-Ajami A, Ramasawmy R, Krishnamoorthy R. Jassim N, et al. Among authors: gerard n. Hemoglobin. 1999 Aug;23(3):213-20. doi: 10.3109/03630269909005701. Hemoglobin. 1999. PMID: 10490133

9

CYP2D6 genetic polymorphism in South Indian populations.

Naveen AT, Adithan C, Soya SS, Gerard N, Krishnamoorthy R. Naveen AT, et al. Among authors: gerard n. Biol Pharm Bull. 2006 Aug;29(8):1655-8. doi: 10.1248/bpb.29.1655. Biol Pharm Bull. 2006. PMID: 16880622 Free article.

10

Spectrum of beta thalassemia mutations and their linkage to beta-globin gene haplotypes in the Indo-Mauritians.

Kotea N, Ramasawmy R, Lu CY, Fa NS, Gerard N, Beesoon S, Ducrocq R, Surrun SK, Nagel RL, Krishnamoorthy R. Kotea N, et al. Among authors: gerard n. Am J Hematol. 2000 Jan;63(1):11-5. doi: 10.1002/(sici)1096-8652(200001)63:1<11::aid-ajh3>3.0.co;2-d. Am J Hematol. 2000. PMID: 10602161 Free article.

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