Zobrazeno 1 - 10
of 28
pro vyhledávání: '"M T, Yacoubi"'
Publikováno v:
Scholars Journal of Medical Case Reports. :492-495
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3402e1a78805129041636fae30d6ae8e
https://doi.org/10.36347/sjmcr.2020.v08i04.021
https://doi.org/10.36347/sjmcr.2020.v08i04.021
Autor:
Nabiha Missaoui, H. Krifa, Moncef Mokni, Boulbeba Selmi, Sihem Hmissa, M. T. Yacoubi, Sarra Limam
Publikováno v:
Cancer investigation. 38(7)
The study investigated the human cytomegalovirus (HCMV) and human papillomavirus (HPV) in gliomas. A retrospective study was conducted on 112 samples. HCMV was investigated by PCR, in situ hybridiz...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15e4014e9c3299ad98ce2c292bcdc87c
https://pubmed.ncbi.nlm.nih.gov/32643440
https://pubmed.ncbi.nlm.nih.gov/32643440
Autor:
Boulbeba Selmi, H. Krifa, Moncef Mokni, Nabiha Missaoui, M. T. Yacoubi, Sarra Limam, Ahlem Bdioui
Publikováno v:
Journal of neurovirology. 26(3)
The gliomagenesis remains not fully established and their etiological factors still remain obscure. Polyomaviruses were detected and involved in several human tumors. Their potential implication in gliomas has been not yet surveyed in Africa and Arab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2b49a859aae67ea9e5343358668ff36
https://pubmed.ncbi.nlm.nih.gov/32124265
https://pubmed.ncbi.nlm.nih.gov/32124265
Autor:
Colin A. Johnson, Valérie Cormier-Daire, Maryse Bonnière, Christel Thauvin-Robinet, Soumaya Mougou-Zerelli, Annick Toutain, Sophie Saunier, Stanislas Lyonnet, Laurence Loeuillet, Bettina Bessières, Sophie Thomas, Christine Bole-Feysot, Marine Legendre, Marie-Anne Barthez, Yves Ville, Tania Attié-Bitach, Caroline Alby, Katarzyna Szymanska, Frédérique Jossic, Patrick Nitschke, Albert David, Dominique Gaillard, M. T. Yacoubi, Michel Vekemans, Férechté Encha-Razavi, Arnold Munnich
Publikováno v:
The American Journal of Human Genetics. 91(2):372-378
Orofaciodigital syndromes (OFDSs) consist of a group of heterogeneous disorders characterized by abnormalities in the oral cavity, face, and digits and associated phenotypic abnormalities that lead to the delineation of 13 OFDS subtypes. Here, by a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70e1b6f9f3d010051e01e2d83bb9acf2
Publikováno v:
Revue de médecine périnatale. 3:148-151
L’anevrisme de la veine de Galien (AVG) est une malformation vasculaire cerebrale complexe, realisant une dilatation pseudoanevrismale de l’ampoule de Galien associee a une ou plusieurs fistules arterioveineuses. C’est une malformation rare tre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8aeaa8700cc2c2337821acfb44db0cc8
https://doi.org/10.1007/s12611-011-0125-9
https://doi.org/10.1007/s12611-011-0125-9
Autor:
T. Kamijo, P. Milart, K. Wojcik, P. Szkodziak, S. Wozniak, P. Czuczwar, T. Paszkowski, H. Landolsi, M. T. Yacoubi, W. Stita, M. Gribaa, S. Hmissa, N. Molenaar, N. H. van Besouw, E. A. P. Steegers, W. Visser, P. de Kuiper, R. de Krijger, N. Exalto, R. Lagrand, S. P. Kaandorp, C. H. M. Mellink, M. van Wely, E. J. W. Redeker, A. C. Knegt, M. Goddijn, C. Vidal, J. Giles, M. Meseguer, J. L. Zuzuarregui, E. Bosch, A. Pellicer, D. Schust, M. Sugimoto, J. Sugimoto, A. D. Reus, M. D. Stephenson, R. R. Krijger de, F. M. Dunne van, C. Exacoustos, E. Vaquero, A. Di Giovanni, V. Romeo, N. Lazzarin, D. Arduini, S. Brahem, M. Mehdi, F. Atig, H. Ghedir, S. Ibala, M. Ajina, A. Saad, C. Chang, H. Wang, S. Huang, S. Pai, Y. Soong, E. Papanikolaou, G. Pantos, G. Grimbizis, E. Bili, N. Polyzos, K. Karastefanou, P. Humaidan, S. Esteves, B. Tarlatzis, K. McNamee, A. Topping, R. G. Farquharson, F. Dawood, M. Ruiz Galdon, A. M. Lendinez, A. R. Palomares, F. Martinez, B. Perez-Nevot, A. Jimenez Fernandez, A. Reyes-Engel, J. A. Horcajadas, R. F. Savaris, V. Kovac, M. Reljic, V. Vlaisavljevic, A. Colicchia, I. Pergolini, B. Gilio, M. R. Rampini, P. Alfano, D. Marconi, C. Verlengia, E. Alviggi, J. Bellver, F. Cruz, M. C. Martinez, J. Ramirez, J. Ferro, N. Garrido, J. K. Brown, K. B. Lauer, N. F. Inglis, H. O. D. Critchley, A. W. Horne, H. Samli, B. Cetinkaya Demir, A. Ozgoz, M. A. Atalay, G. Uncu, Y. Yan, M. A. Cai-hong, Q. I. A. O. Jie, C. H. E. N. Xin-na, C. H. E. Weimar, A. Kavelaars, B. Gellersen, J. J. Brosens, J. M. T. de Vreeden-Elbertse, C. J. Heijnen, N. S. Macklon, J. C. Castillo, M. Dolz, O. Caballero, L. Abad, J. Perez-Panades, F. Bonilla-Musoles, W. Eggert - Kruse, S. Scholz, I. Klopsch, T. Strowitzki
Publikováno v:
Human Reproduction. 26:i151-i160
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::734e4eecf408427338a464e8a8756116
https://doi.org/10.1093/humrep/26.s1.78
https://doi.org/10.1093/humrep/26.s1.78
Autor:
Tamás Marton, Christopher J. Ricketts, Richard C. Trembath, Catherine Fallet-Bianco, Fatimah Rahman, M. T. Yacoubi, Phillip Cox, Mark R. Morris, Esther Meyer, Louise J. Tee, Mudher Al-Adnani, Bettina Bessières, Neil V. Morgan, Shanaz Pasha, David Tannahill, Denise Williams, Anne Bazin, Pierre Dechelotte, Eamonn R. Maher
Publikováno v:
The American Journal of Human Genetics. 86:471-478
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (PVHH), also known as Fowler syndrome, is an autosomal-recessively inherited prenatal lethal disorder characterized by hydranencephaly; brain stem, basal ganglia, and spinal cord di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::088d7f270c6535da4003829ef18b92e5
https://doi.org/10.1016/j.ajhg.2010.02.004
https://doi.org/10.1016/j.ajhg.2010.02.004
Autor:
M. T. Yacoubi, A. Lahmar, H. Landolsi, L. Bouslama, Abdelhalim Trabelsi, S. Korbi, S. Hmissa, Mahjoub Aouni
Publikováno v:
Pathologie Biologie. 57:e1-e7
The aim of the present study was to determine whether there is an association between Parvovirus B19 infection and hydrops fetalis setting in fetus and neonate. Twenty-nine samples were analyzed by three methods. Each sample was histologically examin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98555c603016a9416ca9228a1796dcdf
https://doi.org/10.1016/j.patbio.2007.11.001
https://doi.org/10.1016/j.patbio.2007.11.001
Autor:
Nabiha Missaoui, M. Mokni, B. Sriha, I. Lagueb, M. T. Yacoubi, S. Korbi, M. Trimech, Sihem Hmissa, Amel Trabelsi
Publikováno v:
Annales d'Endocrinologie. 66:333-339
Les nodules thyroidiens sont frequents et posent parfois un probleme de diagnostic et/ou de pronostic. L’etude de la ploidie et l’analyse du cycle cellulaire dans ce type de lesions pourraient etre un moyen de distinction entre une tumeur benigne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3cbf20102758e347a5171f996d988e88
https://doi.org/10.1016/s0003-4266(05)81790-1
https://doi.org/10.1016/s0003-4266(05)81790-1
Autor:
Soumaya Rammeh, M. T. Yacoubi, Sihem Hmissa, O. Gharbi, Sadok Korbi, A. Trabelsi, N. Boujelbene
Publikováno v:
Oncologie. 11:163-165
Nous rapportons un cas de carcinome papillaire se reux de l’ute rus chez une femme de 50 ans, sans ante ce dents particuliers, de couvert sur une pie ce d’annexectomie indiquee pour un kyste ovarien tordu. L’origine ute rine de la tumeur e tait
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07e793294070d21eb4098b5734a55e96
https://doi.org/10.1007/s10269-007-0811-1
https://doi.org/10.1007/s10269-007-0811-1