Zobrazeno 1 - 10
of 141
pro vyhledávání: '"H, Elghezal"'
Publikováno v:
Andrologia. 44:139-143
The aim of this study was to evaluate the incidence of spermatic aneuploidies in men with severe teratozoospermia and to determine an eventual relation between aneuploidies and a specific morphology of spermatozoa. Fluorescence in situ hybridisation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b21147ba87cbe0e2ed3a3149d43ca84b
https://doi.org/10.1111/j.1439-0272.2010.01152.x
https://doi.org/10.1111/j.1439-0272.2010.01152.x
Publikováno v:
Andrologia. 44:130-135
The aim of this study was to analyse the meiotic segregation and DNA fragmentation rates in ejaculated spermatozoa of Tunisian men who presented the macrocephalic sperm head syndrome and to compare the results with those from 20 fertile men with norm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66f8bec3334a743f624574b3371e66dc
https://doi.org/10.1111/j.1439-0272.2010.01115.x
https://doi.org/10.1111/j.1439-0272.2010.01115.x
Autor:
I. Benabdallah, N. Mama, Audrey Labalme, Ali Saad, H. Elghezal, I. Hamdi, Soumaya Mougou-Zerelli, H. Hannachi, Damien Sanlaville
Publikováno v:
Cytogenetic and Genome Research. 135:102-110
We led a clinical and molecular characterization of a patient with mild mental delay and dysmorphic features initially referred for cytogenetic exploration of an azoospermia. We employed FISH and array CGH techniques for a better definition and refin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d031f89460222a662749783b10abdaa7
https://doi.org/10.1159/000330880
https://doi.org/10.1159/000330880
Autor:
B. Acar-Perk, J. Weimer, K. Koch, A. Salmassi, N. Arnold, L. Mettler, A. G. Schmutzler, C. S. Ottolini, D. K. Griffin, A. H. Handyside, M. C. Summers, A. R. Thornhill, D. Montjean, M. Benkhalifa, P. Cohen-Bacrie, J. P. Siffroi, J. Mandelbaum, I. Berthaut, A. Bashamboo, C. Ravel, K. McElreavey, A. Ao, X. Y. Zhang, A. Yilmaz, J. T. Chung, E. Demirtas, W. Y. Son, M. Dahan, W. Buckett, H. Holzer, S. L. Tan, A. Perheentupa, M. Vierula, N. Jorgensen, N. E. Skakkebaek, S. Chantot-Bastaraud, J. Toppari, L. Muzii, M. C. Magli, L. Gioia, M. Mattioli, A. P. Ferraretti, L. Gianaroli, I. Koscinski, E. Elinati, C. Fossard, P. Kuentz, Z. Kilani, A. Demirol, T. Gurgan, F. Schmitt, J. Velez de la Calle, N. Iqbal, N. Louanjli, M. Pasquier, F. Carre-Pigeon, J. Muller, C. Barratt, S. Viville, C. Magli, C. Grugnetti, E. Castelletti, B. Paviglianiti, L. Pepas, P. Braude, J. Grace, V. Bolton, Y. Khalaf, T. El-Toukhy, I. Galeraud-Denis, H. Bouraima, L. Sibert, N. Rives, S. Carreau, F. Janse, L. M. de With, B. C. J. M. Fauser, C. B. Lambalk, J. S. E. Laven, A. J. Goverde, J. C. Giltay, V. De Leo, L. Governini, A. Quagliariello, M. A. Margollicci, P. Piomboni, A. Luddi, H. Miyamura, H. Nishizawa, S. Ota, M. Suzuki, A. Inagaki, H. Egusa, S. Nishiyama, T. Kato, I. Nakanishi, T. Fujita, Y. Imayoshi, A. Markoff, I. Yanagihara, Y. Udagawa, H. Kurahashi, B. Alvaro Mercadal, R. Imbert, I. Demeestere, A. De Leener, Y. Englert, S. Costagliola, A. Delbaere, E. Velilla, A. Colomar, E. Toro, S. Chamosa, J. Alvarez, M. Lopez-Teijon, S. Fernandez, Y. Hosoda, A. Hasegawa, N. Morimoto, Y. Wakimoto, Y. Ito, S. Komori, L. Sati, C. Zeiss, R. Demir, J. McGrath, S. Y. Ku, Y. J. Kim, Y. Y. Kim, H. J. Kim, K. E. Park, S. H. Kim, Y. M. Choi, S. Y. Moon, A. Minor, V. Chow, S. Ma, E. Martinez Mendez, M. Gaytan, A. Linan, A. Pacheco, M. San Celestino, C. Nogales, M. Ariza, D. Cernuda, F. Bronet, A. M. Lendinez Ramirez, A. R. Palomares, B. Perez-Nevot, V. Urraca, A. Ruiz Martin, A. Reche, M. Ruiz Galdon, A. Reyes-Engel, N. R. Treff, X. Tao, D. Taylor, B. Levy, K. M. Ferry, R. T. Scott Jr., S. Vasan, K. K. Acharya, B. Vasan, R. Yalaburgi, K. K. Ganesan, S. C. Darshan, C. H. Neelima, P. Deepa, B. Akhilesh, D. Sravanthi, K. S. Sreelakshmi, H. Deepti, J. H. van Doorninck, C. Eleveld, M. van der Hoeven, E. Birnie, E. A. P. Steegers, R. J. Galjaard, I. M. van den Berg, F. Fiorentino, L. Spizzichino, S. Bono, A. Biricik, G. Kokkali, L. Rienzi, F. M. Ubaldi, E. Iammarrone, A. Gordon, K. Pantos, E. Oitmaa, A. Tammiste, S. Suvi, M. Punab, M. Remm, A. Metspalu, A. Salumets, L. Rodrigo, P. Mir, A. Cervero, E. Mateu, A. Mercader, C. Vidal, J. Giles, J. Remohi, A. Pellicer, J. Martin, C. Rubio, H. Mozdarani, S. Moghbeli Nejad, M. Behmanesh, A. Alleyasin, H. Ghedir, S. Ibala-Romdhane, O. Mamai, S. Brahem, H. Elghezal, M. Ajina, M. Gribaa, A. Saad, M. C. Martinez, V. Peinado, M. Milan, N. Al-Asmar, P. Buendia, A. Delgado, L. Escrich, B. Amorocho, C. Simon, L. Petrussa, H. Van de Velde, N. De Munck, M. De Rycke, S. Altmae, J. A. Martinez-Conejero, F. J. Esteban, M. Ruiz-Alonso, A. Stavreus-Evers, J. A. Horcajadas, B. Bug, G. Raabe-Meyer, U. Bender, J. Zimmer, B. Schulze, P. H. Vogt, T. Laisk, M. Peters, V. Grabar, A. Feskov, E. Zhilkova, N. Sugawara, M. Maeda, T. Seki, T. Manome, R. Nagai, Y. Araki, I. Georgiou, L. Lazaros, N. Xita, A. Chatzikyriakidou, A. Kaponis, N. Grigoriadis, E. Hatzi, I. Grigoriadis, N. Sofikitis, K. Zikopoulos, M. Gunn, P. R. Brezina, A. Benner, L. Du, W. G. Kearns, X. Shen, C. Zhou, Y. Xu, Y. Zhong, Y. Zeng, G. Zhuang, M. C. Gunn, K. Richter, P. Andreeva, I. Dimitrov, M. Konovalova, S. Kyurkchiev, A. Shterev, A. Daser, E. Day, H. Turley, A. Immesberger, T. Haaf, T. Hahn, P. H. Dear, M. Schorsch, J. Don, N. Golan, T. Eldar, R. Yaverboim
Publikováno v:
Human Reproduction. 26:i278-i296
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47617fc5333d6052266255f604512977
https://doi.org/10.1093/humrep/26.s1.89
https://doi.org/10.1093/humrep/26.s1.89
Publikováno v:
Archives de Pédiatrie. 17:1078-1082
Triploidy is one of the most common chromosomal aberrations in spontaneous abortions characterized by a 69-chromosome karyotype. This chromosome abnormality is rare in live-born children. Prevalence is lower than 1/50,000. We report on two premature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e379b7fc9f80ac0c47e9832ac2600b70
https://doi.org/10.1016/j.arcped.2010.03.009
https://doi.org/10.1016/j.arcped.2010.03.009
Publikováno v:
Placenta. 29:454-460
Placental mesenchymal dysplasia (PMD) is a distinct placental disorder that may coexist with a normal fetus. In one-third of cases, the fetus exhibits Beckwith-Wiedemann Syndrome (BWS). In the present study, we report a case of PMD changes associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42bb1885cf1a076a3c851d93951c2c02
https://doi.org/10.1016/j.placenta.2008.01.001
https://doi.org/10.1016/j.placenta.2008.01.001
Autor:
Ali Saad, Mohamed Tahar Sfar, H. Elghezal, A. Bedoui, H. Soua, H. Ben Hamouda, M. Braham, A. Ayadi
Publikováno v:
Journal de Pédiatrie et de Puériculture. 18:354-357
Resume Le syndrome de Jacobsen est caracterise par une deletion partielle de l'extremite distale du bras long du chromosome 11. Son expression phenotypique est tres variable. Il associe une dysmorphie faciale complexe, des malformations cardiaques et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0894fd4dae04bc307b242173d3d189d
https://doi.org/10.1016/j.jpp.2005.09.007
https://doi.org/10.1016/j.jpp.2005.09.007
Publikováno v:
Andrologia. 44
The aim of this study was to evaluate the incidence of spermatic aneuploidies in men with severe teratozoospermia and to determine an eventual relation between aneuploidies and a specific morphology of spermatozoa. Fluorescence in situ hybridisation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0ffc4f277fb8db371df509ca9136e22b
https://pubmed.ncbi.nlm.nih.gov/21848885
https://pubmed.ncbi.nlm.nih.gov/21848885
Publikováno v:
Andrologia. 44(2)
The aim of this study was to analyse the meiotic segregation and DNA fragmentation rates in ejaculated spermatozoa of Tunisian men who presented the macrocephalic sperm head syndrome and to compare the results with those from 20 fertile men with norm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::be51f408fa258891db5a6add4be5d7b3
https://pubmed.ncbi.nlm.nih.gov/21714801
https://pubmed.ncbi.nlm.nih.gov/21714801
Autor:
S, Hadiji Mseddi, L, Kammoun, H, Bellaaj, Y, Ben Youssef, L, Aissaoui, L, Torjemane, F, Telmoudi, A, Amouri, H, Elghezal, M, Ouederni, Y, Ben Abdennebi, S, Hammemi, T, Ben Othmen, H, Ben Abid, M, Bejaoui, S, Abdelhak, M, Hachicha, K, Dellagi, M, Frikha, H, Slama
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 19(5)
Fanconi anemia (FA) is a genetically and phenotypically heterogeneous inherited disease. Many groups have established FA registries. In Tunisia, in collaboration with the Tunisian Fanconi Anemia Study Group (TFASG), we set up the Tunisian Fanconi Ane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1cbc68aa6305e7ad021eeab67c5589b9
https://pubmed.ncbi.nlm.nih.gov/22480464
https://pubmed.ncbi.nlm.nih.gov/22480464