Joly P - Search Results

1

[Beta-thalassemias: molecular, epidemiological, diagnostical and clinical aspects].

Joly P, Pondarre C, Badens C. Joly P, et al. Ann Biol Clin (Paris). 2014 Nov-Dec;72(6):639-68. doi: 10.1684/abc.2014.1015. Ann Biol Clin (Paris). 2014. PMID: 25486662 Free article. Review. French.

2

Identification and molecular characterization of four new large deletions in the beta-globin gene cluster.

Joly P, Lacan P, Garcia C, Couprie N, Francina A. Joly P, et al. Blood Cells Mol Dis. 2009 Jul-Aug;43(1):53-7. doi: 10.1016/j.bcmd.2009.01.017. Epub 2009 Mar 9. Blood Cells Mol Dis. 2009. PMID: 19269866

3

[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. 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.

4

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: joly p. 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

5

[Flowcharts for the diagnosis and the molecular characterization of hemoglobinopathies].

Aguilar-Martinez P, Badens C, Bonello-Palot N, Cadet E, Couque N, Ducrocq R, Elion J, Francina A, Joly P, Pissard S, Rochette J; Réseay DHOS Pathologie héréditaire de l'érythrocyte. Aguilar-Martinez P, et al. Among authors: joly p. Ann Biol Clin (Paris). 2010 Jul-Aug;68(4):455-64. doi: 10.1684/abc.2010.0457. Ann Biol Clin (Paris). 2010. PMID: 20650741 Free article. French.

6

Severe β-thalassemia intermedia in a compound heterozygous patient for the -30 (T>A) β(+)-thalassemia mutation and the δ(0)β(+)-Senegalese deletion.

Griffon C, Joly P, Sénéchal A, Philit F, Francina A. Griffon C, et al. Among authors: joly p. Hemoglobin. 2010;34(5):505-8. doi: 10.3109/03630269.2010.509230. Hemoglobin. 2010. PMID: 20854126

7

Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the disease.

Badens C, Joly P, Agouti I, Thuret I, Gonnet K, Fattoum S, Francina A, Simeoni MC, Loundou A, Pissard S. Badens C, et al. Among authors: joly p. Haematologica. 2011 Nov;96(11):1712-4. doi: 10.3324/haematol.2011.046748. Epub 2011 Jul 26. Haematologica. 2011. PMID: 21791466 Free PMC article. Clinical Trial.

8

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. Hemoglobin. 2011;35(4):316-22. doi: 10.3109/03630269.2011.571331. Hemoglobin. 2011. PMID: 21797698

9

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. 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

10

[Place of genotyping in addition to the phenotype and the assay of serum α-1 antitrypsin].

Joly P, Francina A, Lacan P, Heraut J, Chapuis-Cellier C. Joly P, et al. Ann Biol Clin (Paris). 2011 Sep-Oct;69(5):571-6. doi: 10.1684/abc.2011.0613. Ann Biol Clin (Paris). 2011. PMID: 22008137 Free article. French.

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