JOLY Philippe

JOLY Philippe

Etablissement d'appartenance : Université Claude Bernard Lyon 1

Adresse mail : philippe.joly@chu-lyon.fr

Ligne directe : 04-72-11-06-35

 

Position : Praticien hospitalier

Domaine de recherche : Drépanocytose – Gènes modificateurs – Thalassémie‐ Rhéologie

Thématique(s) :

Thématique 1, Biologie vasculaire et du globule rouge (BVGR)

5 Publications :

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. G6PD deficiency and absence of α‐thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia.Eur J Haematol. 2015 Jun 13. doi: 10.1111/ejh.12607. 

Danjou F, Francavilla M, Anni F, Satta S, Demartis FR, Perseu L, Manca M, Sollaino MC, Manunza L, Mereu E, Marceddu G, Pissard S, Joly P, Thuret I, Origa R, Borg J, Forni GL, Piga A, Lai ME, Badens C, Moi P, Galanello R. A genetic score for the prediction of beta‐thalassemia severity. Haematologica. 2015 Apr;100(4):452‐7. doi: 10.3324/haematol.2014.113886. Epub 2014 Dec 5. 

Vinatier I, Martin X, Costa JM, Bazin A, Giraudier S, Joly P. A late onset sickle cell disease reveals a mosaic segmental uniparental isodisomy of chromosome 11p15. Blood Cells Mol Dis. 2015 Jan;54(1):53‐5. doi: 10.1016/j.bcmd.2014.07.021. Epub 2014 Aug 20. Review. 

Joly P, Gagnieu MC, Bardel C, Francina A, Pondarre C, Martin C. Genotypic screening of the main opiate‐related polymorphisms in a cohort of 139 sickle cell disease patients. Am J Hematol. 2012 May;87(5):534‐6. doi: 10.1002/ajh.23137. Epub 2012 Mar 19. 

Joly P, Pondarré C, Bardel C, Francina A, Martin C. The alpha‐globin genotype does not influence sickle cell disease severity in a retrospective cross‐validation study of the pediatric severity score. Eur J Haematol. 2012 Jan;88(1):61‐7. doi: 10.1111/j.1600‐0609.2011.01705.x. Epub 2011 Nov 15