Contribution à l'étude de la régulation des gènes de globines. Clonage et études de deux régions régulatrices = Contribution to the globin genes regulation study cloning and studies of two regulating regionsPissard, Serge; Romèo, P.-H.1996, 120 p.Thesis

Le diagnostic prénatal de la drépanocytoseTOUBOUL, Claudine; BACHIR, Dora; PISSARD, Serge et al.MTP. Médecine thérapeutique pédiatrie. 2008, Vol 11, Num 1, pp 12-16, issn 1286-5494, 5 p.Article

HFE genotyping by amplification refractory mutation system-denaturing HPLCPISSARD, Serge; HUYNH, Lam-Thuy-Ai; MARTIN, Josiane et al.Clinical chemistry (Baltimore, Md.). 2002, Vol 48, Num 5, pp 769-772, issn 0009-9147Article

Does Liebig's law of the minimum scale up from species to communities?DANGER, Michael; DAUFRESNE, Tanguy; LUCAS, Francoise et al.Oikos (København). 2008, Vol 117, Num 11, pp 1741-1751, issn 0030-1299, 11 p.Article

A novel (εγδβ)°-thalassemia deletion associated with an a globin gene triplication leading to a severe transfusion dependant fetal thalassemic syndromeROSE, Christian; ROSSIGNOL, Julien; LAMBILLIOTTE, Anne et al.Haematologica (Roma). 2009, Vol 94, Num 4, pp 593-594, issn 0390-6078, 2 p.Article

Hydroxyurea can eliminate transfusion requirements in children with severe β-thalassemiaBRADAI, Mohamed; MOHAND TAYEB ABAD; PISSARD, Serge et al.Blood. 2003, Vol 102, Num 4, pp 1529-1530, issn 0006-4971, 2 p.Article

Thalassemia in the indigenous population of brittany : Identification of three rare mutationsJAMET, Déborah; PISSARD, Serge; BLOUCH, Marie-Thérèse et al.Haematologica (Roma). 2006, Vol 91, Num 10, pp 1418-1419, issn 0390-6078, 2 p.Article

Pyruvate kinase deficiency in france : a 3-year study reveals 27 new mutationsPISSARD, Serge; MAX-AUDIT, Isabelle; SKOPINSKI, Laurent et al.British journal of haematology. 2006, Vol 133, Num 6, pp 683-689, issn 0007-1048, 7 p.Article

New variant of unclassified congenital dyserythropoietic anaemia: the concept of the erythroid regulator?GAY, Julie; FOURNIER, Martine; PIERRE-EUGENE, Cecile et al.British journal of haematology. 2012, Vol 157, Num 1, pp 148-151, issn 0007-1048, 4 p.Article

Perinatal zidovudine prophylaxis in HIV type-1-infected pregnant women with thalassaemia carriage in ThailandBRIAND, Nelly; PORNPRASERT, Sakorn; NGO-GIANG-HUONG, Nicole et al.Antiviral therapy (London). 2009, Vol 14, Num 1, pp 117-122, issn 1359-6535, 6 p.Article

Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysisBARTOLUCCI, Pablo; BRUGNARA, Carlo; TEIXEIRA-PINTO, Armando et al.Blood. 2012, Vol 120, Num 15, pp 3136-3141, issn 0006-4971, 6 p.Article

Practical approach for characterization of glucose 6-phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: Description of seven new G6PD mutantsMORADKHANI, Kamran; MEKKI, Chadia; BAHUAU, Michel et al.American journal of hematology. 2012, Vol 87, Num 2, pp 208-210, issn 0361-8609, 3 p.Article

Evaluation of the free α-hemoglobin pool in red blood cells: A new test providing a scale of β-thalassemia severityVASSEUR, Corinne; PISSARD, Serge; DOMINGUES-HAMDI, Elisa et al.American journal of hematology. 2011, Vol 86, Num 2, pp 199-202, issn 0361-8609, 4 p.Article

A novel mutation of the β-globin gene promoter (-102 C>A) and pitfalls in family screeningAGUILAR-MARTINEZ, Patricia; JOURDAN, Eric; BRUN, Sophie et al.American journal of hematology. 2007, Vol 82, Num 12, pp 1088-1090, issn 0361-8609, 3 p.Article

Severe hemolytic anemia in a Vietnamese family, associated with novel mutations in the gene encoding for pyruvate kinaseCOSTA, Catherine; ALBUISSON, Juliette; LETHI HAO et al.Haematologica (Roma). 2005, Vol 90, Num 1, pp 25-30, issn 0390-6078, 6 p.Article

FGFR3 and TP53 gene mutations define two distinct pathways in urothelial cell carcinoma of the bladderBAKKAR, Ashraf A; WALLERAND, Herve; THIERY, Jean-Paul et al.Cancer research (Baltimore). 2003, Vol 63, Num 23, pp 8108-8112, issn 0008-5472, 5 p.Article

Recommandations pour la (bonne) pratique du diagnostic moléculaire de l'hémochromatose liée au gène HFE* Synthèse d'une enquête réalisée auprès du réseau national des laboratoires pratiquant le diagnostic de maladies rares du métabolisme du fer = Molecular diagnosis of HFE mutations in routine laboratories Results of a survey from reference laboratories in FranceJOUANOLLE, Anne-Marie; GEROLAMI, Victoria; GED, Cécile et al.Annales de biologie clinique (Paris). 2012, Vol 70, Num 3, pp 305-313, issn 0003-3898, 9 p.Article

Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the diseaseBADENS, Catherine; JOLY, Philippe; AGOUTI, Imane et al.Haematologica (Roma). 2011, Vol 96, Num 11, pp 1712-1714, issn 0390-6078, 3 p.Article

Arbres décisionnels pour le diagnostic et la caractérisation moléculaire des hémoglobinopathies = Flowcharts for the diagnosis and the molecular characterization of hemoglobinopathiesAGUILAR-MARTINEZ, Patricia; BADENS, Catherine; ROCHETTE, Jacques et al.Annales de biologie clinique (Paris). 2010, Vol 68, Num 4, pp 455-464, issn 0003-3898, 10 p.Article

Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermediaBRADAI, Mohamed; PISSARD, Serge; TAYEB ABAD, Mohand et al.Transfusion (Philadelphia, PA). 2007, Vol 47, Num 10, pp 1830-1836, issn 0041-1132, 7 p.Article

Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletionsPUEHRINGER, Helene; NAJMABADI, Hossein; AL-ATEEQ, Suad et al.Clinical chemistry and laboratory medicine. 2007, Vol 45, Num 5, pp 605-610, issn 1434-6621, 6 p.Article