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Items: 9


Intravenous immunoglobulin in patients with acquired Von Willebrand syndrome: A single referral centre experience.

Bertolino J, Ibrahim M, Seguier J, Masson E, Bernit E, Veit V, Ebbo M, Harlé JR, Khibri H, Pouymayou C, Morange PE, Schleinitz N.

Haemophilia. 2019 Jan;25(1):e42-e45. doi: 10.1111/hae.13639. Epub 2018 Nov 21. No abstract available.


Macrothrombocytopenia and dense granule deficiency associated with FLI1 variants: ultrastructural and pathogenic features.

Saultier P, Vidal L, Canault M, Bernot D, Falaise C, Pouymayou C, Bordet JC, Saut N, Rostan A, Baccini V, Peiretti F, Favier M, Lucca P, Deleuze JF, Olaso R, Boland A, Morange PE, Gachet C, Malergue F, Fauré S, Eckly A, Trégouët DA, Poggi M, Alessi MC.

Haematologica. 2017 Jun;102(6):1006-1016. doi: 10.3324/haematol.2016.153577. Epub 2017 Mar 2.


Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.

Noris P, Schlegel N, Klersy C, Heller PG, Civaschi E, Pujol-Moix N, Fabris F, Favier R, Gresele P, Latger-Cannard V, Cuker A, Nurden P, Greinacher A, Cattaneo M, De Candia E, Pecci A, Hurtaud-Roux MF, Glembotsky AC, Muñiz-Diaz E, Randi ML, Trillot N, Bury L, Lecompte T, Marconi C, Savoia A, Balduini CL, Bayart S, Bauters A, Benabdallah-Guedira S, Boehlen F, Borg JY, Bottega R, Bussel J, De Rocco D, de Maistre E, Faleschini M, Falcinelli E, Ferrari S, Ferster A, Fierro T, Fleury D, Fontana P, James C, Lanza F, Le Cam Duchez V, Loffredo G, Magini P, Martin-Coignard D, Menard F, Mercier S, Mezzasoma A, Minuz P, Nichele I, Notarangelo LD, Pippucci T, Podda GM, Pouymayou C, Rigouzzo A, Royer B, Sie P, Siguret V, Trichet C, Tucci A, Saposnik B, Veneri D; European Hematology Association – Scientific Working Group on Thrombocytopenias and Platelet Function Disorders.

Haematologica. 2014 Aug;99(8):1387-94. doi: 10.3324/haematol.2014.105924. Epub 2014 Apr 24.


The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (A{alpha}Cys36Gly, A{alpha}Cys36Arg and A{alpha}Cys45Tyr) confirms the role of N-terminal A{alpha} disulfide bonds in protein assembly and secretion.

Hanss M, Pouymayou C, Blouch MT, Lellouche F, Ffrench P, Rousson R, Abgrall JF, Morange PE, Quélin F, de Mazancourt P.

Haematologica. 2011 Aug;96(8):1226-30. doi: 10.3324/haematol.2010.029801. Epub 2011 Apr 1.


Molecular characterization of a novel mutation in the factor XIII a subunit gene associated with a severe defect: importance of prophylactic substitution.

Morange P, Trigui N, Frère C, Chambost H, Pouymayou C, Uters M, Boucly C, Juhan-Vague I, de Mazancourt P.

Blood Coagul Fibrinolysis. 2009 Oct;20(7):605-6. doi: 10.1097/MBC.0b013e32832ee7eb.


Prospective analysis of factor XI deficiencies in the Marseilles area identified four novel mutations among 12 consecutive unrelated families.

Quélin F, Frère C, Pouymayou C, Morange P, de Mazancourt P, Juhan-Vague I.

Blood Coagul Fibrinolysis. 2009 Jan;20(1):84-8. doi: 10.1097/MBC.0b013e32831bc51c.


Molecular characterization of a novel mutation in the factor XIII A subunit gene associated with a severe defect and an adulthood diagnosis.

Trigui N, Frère C, D'Ercole C, Chambost H, Chapuis N, Pouymayou C, Morange P, de Mazancourt P.

Haemophilia. 2007 Mar;13(2):221-2. No abstract available.


[Indications for orthophony therapy in written language disorders in children. Work Group assembled by the National Agency for Health Accreditation and Evaluation (ANAES)].

Pouymayou C, David L.

Ann Otolaryngol Chir Cervicofac. 1998 Oct;115 Suppl 1:S75-88. Review. French. No abstract available.


[Apropos of 2 cases of severe malaria contracted in the port of Marseille].

Delmont J, Brouqui P, Poullin P, Pouymayou C, Faugere B, Ottomani A, Gabriel B, Bourgeade A.

Bull Soc Pathol Exot. 1995 Mar;88(4):170-3. French.


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