Saint-Martin C - Search Results

1

Hemoglobin Hekinan [alpha (2)27(B8)Glu----Asp beta 2] detected in Guyana.

Merault G, Keclard L, Desfontaines L, Saint-Martin C, Blouquit Y, Rosa J, Galacteros F. Merault G, et al. Hemoglobin. 1989;13(4):397-402. doi: 10.3109/03630268909003402. Hemoglobin. 1989. PMID: 2753738 No abstract available.

2

Hemoglobin sickle-lepore: an unusual case of sickle cell disease.

Romana M, Diara JP, Merghoub T, Kéclard L, Saint-Martin C, Berchel C, Mérault G. Romana M, et al. Acta Haematol. 1997;98(3):170-1. doi: 10.1159/000203615. Acta Haematol. 1997. PMID: 9352751 No abstract available.

3

Diverse genetic mechanisms operate to generate atypical betaS haplotypes in the population of Guadeloupe.

Romana M, Kéclard L, Froger A, Lavocat E, Saint-Martin C, Berchel C, Mérault G. Romana M, et al. Hemoglobin. 2000 May;24(2):77-87. doi: 10.3109/03630260009003426. Hemoglobin. 2000. PMID: 10870878

4

Sickle cell disorder, beta-globin gene cluster haplotypes and alpha-thalassemia in neonates and adults from Guadeloupe.

Kéclard L, Romana M, Lavocat E, Saint-Martin C, Berchel C, Mérault G. Kéclard L, et al. Am J Hematol. 1997 May;55(1):24-7. doi: 10.1002/(sici)1096-8652(199705)55:1<24::aid-ajh4>3.0.co;2-5. Am J Hematol. 1997. PMID: 9136913 Free article.

5

Hemoglobin Roseau-Pointe a Pitre alpha 2 beta 2(90) (F6) Glu----Gly: a new hemoglobin variant with slight instability and low oxygen affinity.

Merault G, Keclard L, Saint-Martin C, Jasmin K, Campier A, Delanoe-Garin J, Arous N, Fortune R, Theodore M, Seytor S, et al. Merault G, et al. FEBS Lett. 1985 May 6;184(1):10-3. doi: 10.1016/0014-5793(85)80642-6. FEBS Lett. 1985. PMID: 3838727 Free article.

6

Molecular characterization of beta-thalassemia mutations in Guadeloupe.

Romana M, Keclard L, Guillemin G, Lavocat E, Saint-Martin C, Berchel C, Mérault G. Romana M, et al. Am J Hematol. 1996 Dec;53(4):228-33. doi: 10.1002/(SICI)1096-8652(199612)53:4<228::AID-AJH3>3.0.CO;2-#. Am J Hematol. 1996. PMID: 8948659 Free article.

7

Efficiency of prenatal counselling for sickle cell disease in Guadeloupe.

Alexandre L, Keclard L, Romana M, Saint-Martin C, Lavocat-Bernard E, Midonet N, Diara JP, Petras M, Berchel C, Merault G. Alexandre L, et al. Genet Couns. 1997;8(1):25-32. Genet Couns. 1997. PMID: 9101275

8

Beta-globin gene cluster haplotypes and alpha-thalassemia in sickle cell disease patients from Trinidad.

Jones-Lecointe A, Smith E, Romana M, Gilbert MG, Charles WP, Saint-Martin C, Kéclard L. Jones-Lecointe A, et al. Am J Hum Biol. 2008 May-Jun;20(3):342-4. doi: 10.1002/ajhb.20732. Am J Hum Biol. 2008. PMID: 18257074

9

Isoelectric focusing of human hemoglobins.

Beuzard Y, Galacteros F, Braconnier F, Dubart A, Chen-Marotel J, Caburi-Martin J, Monplaisir N, Sellaye M, Saint Martin C, Seytor S, Basset P, Rosa J. Beuzard Y, et al. Prog Clin Biol Res. 1981;60:177-95. Prog Clin Biol Res. 1981. PMID: 6169090

10

Phenotypic expression and origin of the rare beta-thalassemia splice site mutation HBB:c.315 + 1G>T.

Broquere C, Brudey K, Harteveld CL, Saint-Martin C, Elion J, Giordano PC, Romana M. Broquere C, et al. Hemoglobin. 2010 Jun;34(3):322-6. doi: 10.3109/03630269.2010.484956. Hemoglobin. 2010. PMID: 20524821

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