Zobrazeno 1 - 10
of 58
pro vyhledávání: '"M. T. Sfar"'
Autor:
H. Jouini, M. T. Sfar, Alessandro Casini, M. Becheur, B. Mahjoub, P. De Moerloose, Taieb Messaoud, Yessine Amri, Rym Dabboubi, Nour El Houda Toumi
Publikováno v:
Haemophilia, Vol. 23, No 4 (2017) pp. e340-e347
Introduction Congenital dysfibrinogenemia is a rare qualitative fibrinogen deficiency. Molecular defects that result in dysfibrinogenemia are usually caused by mutations which affect fibrinopeptide release, fibrin polymerization, fibrin cross-linking
Autor:
E. C. Dul, C. M. A. van Ravenswaaij-Arts, H. Groen, J. van Echten-Arends, J. A. Land, Y. Tyulenev, V. Naumenko, L. Kurilo, L. Shileiko, A. Segal, R. Klimova, A. Kushch, J. Ribas-Maynou, A. Garcia-Peiro, C. Abad, M. J. Amengual, J. Benet, J. Navarro, A. Colasante, A. M. Lobascio, F. Scarselli, M. G. Minasi, E. Alviggi, P. Rubino, V. Casciani, R. Pena, M. T. Varricchio, K. Litwicka, S. Ferrero, D. Zavaglia, G. Franco, Z. P. Nagy, E. Greco, L. Romany, M. Meseguer, S. Garcia-Herrero, A. Pellicer, N. Garrido, A. Dam, A. Pijnenburg, J. C. Hendriks, J. R. Westphal, L. Ramos, J. A. M. Kremer, F. Eertmans, V. Bogaert, B. Puype, W. Geisler, C. Clusmann, I. Klopsch, T. Strowitzki, W. Eggert-Kruse, R. Maettner, E. Isachenko, V. Isachenko, E. Strehler, K. Sterzik, G. Band, I. Madgar, H. Brietbart, Z. Naor, J. S. Cunha-Filho, C. A. Souza, V. G. Krebs, K. D. Santos, W. J. Koff, A. Stein, I. Hammoud, M. Albert, M. Bergere, M. Bailly, F. Boitrelle, F. Vialard, R. Wainer, V. Izard, J. Selva, P. Cohen - Bacrie, S. Belloc, J. de mouzon, M. Cohen-Bacrie, S. Alvarez, A. M. Junca, M. Dumont, S. Douard, N. Prisant, K. Tomita, S. Hashimoto, Y. Akamatsu, M. Satoh, R. Mori, T. Inoue, Y. Ohnishi, K. Ito, Y. Nakaoka, Y. Morimoto, V. J. H. Smith, K. K. Ahuja, F. Atig, M. Raffa, M. T. Sfar, A. Saad, M. Ajina, D. P. A. F. Braga, G. Halpern, R. C. S. Figueira, A. S. Setti, A. Iaconelli Jr., E. Borges Jr., G. S. Medeiros, E. B. Pasqualotto, F. F. Pasqualotto, M. Nadalini, N. Tarozzi, M. Di Santo, A. Borini, C. Lopez-Fernandez, F. Arroyo, P. Caballero, R. Nunez-Calonge, J. L. Fernandez, J. Gosalvez, A. Gosalbez, S. Cortes, K. Zikopoulos, L. Lazaros, G. Vartholomatos, A. Kaponis, G. Makrydimas, N. Plachouras, N. Sofikitis, S. Kalantaridou, E. Hatzi, I. Georgiou, J. de Mouzon, E. Amar, P. Cohen-Bacrie, M. L. Vuillaume, F. Brugnon, C. Artonne, L. Janny, H. Pons-Rejraji, J. Fedder, L. Bosco, G. Ruvolo, A. M. Bruccoleri, M. Manno, M. C. Roccheri, E. Cittadini, I. Bochev, P. Gavrilov, S. Kyurkchiev, A. Shterev, G. Carlomagno, M. Colone, R. A. Condorelli, A. Stringaro, A. E. Calogero, J. Zakova, M. Kralikova, I. Crha, P. Ventruba, J. Melounova, M. Matejovicova, M. Vodova, E. Lousova, M. Sanchez Toledo, C. Alvarez LLeo, C. Garcia Garrido, M. Resta Serra, L. L. Belmonte Andujar, G. Gonzalez de Merlo, M. Pohanka, M. Huser, I. Amiri, J. Karimi, M. T. Goodarzi, H. Tavilani, A. Filannino, M. C. Magli, E. Boudjema, A. Crippa, A. P. Ferraretti, L. Gianaroli, F. Robles, H. Huang, D. J. Yao, H. J. Huang, J. R. Li, S. K. Fan, M. L. Wang, S. Yung-Kuei, S. Amer, A. Mahran, J. Darne, R. Shaw, E. Borghi, C. Cetera, U. Shukla, D. Ogutu, B. Deval, M. Jansa, M. Savvas, N. Narvekar, P. Houska, A. L. Dackland, L. Bjorndahl, U. Kvist, L. Muzii, B. Barboni, L. Samanta, S. Kar, S. A. Yakovenko, M. N. Troshina, B. K. Rutman, S. A. Dyakonov, E. Holmes, C. Feijo, S. Verza Junior, S. C. Esteves, C. L. Berta, A. M. Caille, S. A. Ghersevich, C. Zumoffen, M. J. Munuce, M. San Celestino, D. Agudo, M. Alonso, P. Sanjurjo, D. Becerra, F. Bronet, J. A. Garcia-Velasco, A. Pacheco, R. Lafuente, G. Lopez, M. A. Checa, R. Carreras, M. Brassesco, M. Oneta, V. Savasi, B. Parrilla, D. Guarneri, A. Laureti, F. Pagano, I. Cetin, E. Ekwurtzel, G. Morgante, P. Piomboni, A. Stendardi, F. Serafini, V. De Leo, R. Focarelli, M. Benkhalifa, J. De Mouzon, F. Entezami, A. Junca, J. J. De Mouzon, A. Mangiarini, E. Capitanio, A. Paffoni, L. Restelli, C. Guarneri, C. Scarduelli, G. Ragni, K. Harrison, J. Irving, N. Martin, D. Sherrin, A. Yazdani, C. Almeida, S. Correia, E. Rocha, A. Alves, M. Cunha, L. Ferraz, S. Silva, M. Sousa, A. Barros, A. Perdrix, A. Travers, J. P. Milazzo, F. Clatot, N. Mousset-Simeon, B. Mace, N. Rives, H. S. Clarke, A. Callow, D. Saxton, A. A. Pacey, O. Sapir, G. Oron, A. Ben-Haroush, R. Garor, D. Feldberg, H. Pinkas, A. Wertheimer, B. Fisch, E. Palacios, M. C. Gonzalvo, A. Clavero, J. P. Ramirez, A. Rosales, J. Mozas, J. A. Castilla, J. Mugica, O. Ramon, A. Valdivia, A. Exposito, L. Casis, R. Matorras, R. Bongers, F. Gottardo, M. Zitzmann, S. Kliesch, T. Cordes, A. Kamischke, A. Schultze-Mosgau, N. Buendgen, K. Diedrich, G. Griesinger, L. Crisol, F. Aspichueta, M. L. Hernandez, J. I. Ruiz-Sanz, R. Mendoza, A. A. Sanchez-Tusie, A. Bermudez, P. Lopez, G. C. Churchill, C. L. Trevino, I. Maldonado, J. Dabbah
Publikováno v:
Human Reproduction. 26:i123-i148
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 24(2)
The beta-thalassemia trait is a heterozygous beta-thalassemia characterized by a partial deficiency of the synthesis of beta-globin chains of hemoglobin. It is usually asymptomatic and the diagnosis is often made on the occasion of the completion of
Autor:
H, Ben Hamouda, H, Bouchahda, S, Ghanmi, S, Wannes, H, Soua, H, Hamza, M, Belghith, A, Nouri, M T, Sfar
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 24(9)
Ureterocele is a rare urologic disorder characterized by pseudocystic dilatation of the terminal submucosal ureter. Most cases of ureteroceles are associated with complete ureteral duplicity and ureterohydronephrosis, whereas ureteroceles on simplex
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 23(3)
Imperforate hymen is the most frequent congenital malformation of the female genital tract and usually remains asymptomatic until puberty. The diagnosis of this malformation is rarely made at birth and surgical treatment is often by hymenotomy. Howev
Autor:
Ibtissem Ghedira, Y. Thabet, Amani Mankaï, A. Achour, M. T. Sfar, A. Trabelsi, F. Amri, Abdelaziz Harbi, Wahiba Sakly
Publikováno v:
Journal of Clinical & Cellular Immunology.
Aim: To determine the clinical and serological characteristics in pediatric systemic lupus erythematosus (SLE). Patients and methods: This retrospective study included 37 patients with SLE. All patients fulfilled the ACR revised criteria for SLE and
Autor:
Abdelkarim Ayadi, F Amri, Ibtissem Ghedira, Moncef Jeddi, A.S. Essoussi, R Sghiri, Abdelaziz Harbi, M. T. Sfar, S. Korbi
Publikováno v:
Pathologie Biologie. 49:47-52
Coeliac disease is associated with gluten intolerance in genetically predisposed subjects. Environmental factors, particularly of viral origin, may also play a major role. In this study, the presence of IgA class anti-endomysium antibodies (AEA-IgA),
Autor:
S, Younes-Mhenni, M, Aissi, N, Mokni, A, Boughammoura-Bouatay, S, Chebel, M, Frih-Ayed, A, Kerkeni, M, Bost, G, Chazot, M T, Sfar, M H, Sfar
Publikováno v:
La Tunisie medicale. 91(6)
Parkinson's disease (PD) is a progressive neurodegenerative disorder. The etiology of this disease is still not fully clear, but free radicals have been proposed to cause neuronal injury. Metals play a key role in the intracellular oxidative balance.
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 20(9)
To study the epidemiological, clinical, and bacteriological aspects as well as the outcome of neonatal bacterial meningitis and analyze the factors of poor prognosis of this condition.We report a retrospective analysis of 44 cases of neonatal bacteri
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 19(7)