Francina A - Search Results

1

G6PD deficiency and absence of α-thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia.

Joly P, Garnier N, Kebaili K, Renoux C, Dony A, Cheikh N, Renard C, Ceraulo A, Cuzzubbo D, Pondarré C, Martin C, Pialoux V, Francina A, Bertrand Y, Connes P. Joly P, et al. Among authors: francina a. Eur J Haematol. 2016 Apr;96(4):404-8. doi: 10.1111/ejh.12607. Epub 2015 Jun 30. Eur J Haematol. 2016. PMID: 26072930

2

The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score.

Joly P, Pondarré C, Bardel C, Francina A, Martin C. Joly P, et al. Among authors: francina a. Eur J Haematol. 2012 Jan;88(1):61-7. doi: 10.1111/j.1600-0609.2011.01705.x. Epub 2011 Nov 15. Eur J Haematol. 2012. PMID: 21910753

3

Rapid genotyping of two common G6PD variants, African (A-) and Mediterranean, by high-resolution melting analysis.

Joly P, Lacan P, Garcia C, Martin C, Francina A. Joly P, et al. Among authors: francina a. Clin Biochem. 2010 Jan;43(1-2):193-7. doi: 10.1016/j.clinbiochem.2009.09.012. Epub 2009 Sep 24. Clin Biochem. 2010. PMID: 19782058

4

Genotypic screening of the main opiate-related polymorphisms in a cohort of 139 sickle cell disease patients.

Joly P, Gagnieu MC, Bardel C, Francina A, Pondarre C, Martin C. Joly P, et al. Among authors: francina a. Am J Hematol. 2012 May;87(5):534-6. doi: 10.1002/ajh.23137. Epub 2012 Mar 19. Am J Hematol. 2012. PMID: 22430884 Free article.

5

Massive haemolysis and methaemalbuminaemia in a patient with decompensated haemoglobin H disease.

Joly P, Richard Colmant G, Varennes A, Francina A, Coppéré B, Delacour H. Joly P, et al. Among authors: francina a. Br J Haematol. 2013 Oct;163(1):2. doi: 10.1111/bjh.12499. Epub 2013 Aug 9. Br J Haematol. 2013. PMID: 23931827 Free article. No abstract available.

6

Hemorheology, sickle cell trait, and alpha-thalassemia in athletes: effects of exercise.

Monchanin G, Connes P, Wouassi D, Francina A, Djoda B, Banga PE, Owona FX, Thiriet P, Massarelli R, Martin C. Monchanin G, et al. Among authors: francina a. Med Sci Sports Exerc. 2005 Jul;37(7):1086-92. doi: 10.1249/01.mss.0000170128.78432.96. Med Sci Sports Exerc. 2005. PMID: 16015123

7

Plasma levels of adhesion molecules ICAM-1 and VCAM-1 in athletes with sickle cell trait with or without alpha-thalassemia during endurance exercise and recovery.

Monchanin G, Serpero LD, Connes P, Tripette J, Wouassi D, Francina A, Massarelli R, Gozal D, Thiriet P, Martin C. Monchanin G, et al. Among authors: francina a. Clin Hemorheol Microcirc. 2008;40(2):89-97. Clin Hemorheol Microcirc. 2008. PMID: 19029634

8

[Library of variants (LOV) v. 1.0: an help for the interpretation of the phenotypic haemoglobin data obtained with liquid chromatography Bio-Rad devices].

Joly P, Wajcman H, Francina A. Joly P, et al. Among authors: francina a. Ann Biol Clin (Paris). 2010 Mar-Apr;68(2):254-6. doi: 10.1684/abc.2010.0423. Ann Biol Clin (Paris). 2010. PMID: 20348055 Free article. French.

9

The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patients.

Nguyen TK, Joly P, Bardel C, Moulsma M, Bonello-Palot N, Francina A. Nguyen TK, et al. Among authors: francina a. Blood Cells Mol Dis. 2010 Aug 15;45(2):124-7. doi: 10.1016/j.bcmd.2010.04.002. Epub 2010 May 15. Blood Cells Mol Dis. 2010. PMID: 20472475

10

A novel deletion/insertion caused by a replication error in the β-globin gene locus control region.

Joly P, Lacan P, Garcia C, Meley R, Pondarré C, Francina A. Joly P, et al. Among authors: francina a. Hemoglobin. 2011;35(4):316-22. doi: 10.3109/03630269.2011.571331. Hemoglobin. 2011. PMID: 21797698

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