Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Orru, Sandro"'
Autor:
Grandi, Nicole, Cusano, Roberto, Piras, Giovanna, Fiamma, Maura, Monne, Maria Itria, Fancello, Tatiana, Milia, Jessica, Orrù, Sandro, Scognamiglio, Sante, Serra, Caterina, Mameli, Giuseppe, Uzzau, Sergio, Orrù, Germano, Palmas, Angelo Domenico, Rubino, Salvatore, Tramontano, Enzo
Publikováno v:
In Journal of Infection and Public Health August 2024 17(8)
Autor:
Caocci, Giovanni, Greco, Marianna, Arras, Marcella, Cusano, Roberto, Orrù, Sandro, Martino, Bruno, Abruzzese, Elisabetta, Galimberti, Sara, Mulas, Olga, Trucas, Marcello, Littera, Roberto, Lai, Sara, Carcassi, Carlo, La Nasa, Giorgio
Publikováno v:
In Leukemia Research October 2017 61:1-5
Autor:
Daoud, Hussein, Papadima, Eleni Merkouri, Ouled Amar Bencheikh, Bouchra, Katsila, Theodora, Dionne-Laporte, Alexandre, Spiegelman, Dan, Dion, Patrick A., Patrinos, George P., Orrù, Sandro, Rouleau, Guy A.
Publikováno v:
In European Journal of Medical Genetics November 2015 58(11):573-577
Autor:
Orru, Sandro1 (AUTHOR), Papoulidis, Ioannis2 (AUTHOR), Siomou, Elisavet2 (AUTHOR), Papadimitriou, Dimitrios T.3,4 (AUTHOR), Sotiriou, Sotirios4 (AUTHOR), Nikolaidis, Petros5 (AUTHOR), Eleftheriades, Makarios6 (AUTHOR), Papanikolaou, Evaggelos7 (AUTHOR), Thomaidis, Loretta8 (AUTHOR), Manolakos, Emmanouil1,2,8 (AUTHOR) manolakos@atg-labs.gr
Publikováno v:
Biomedical Reports. Jun2019, Vol. 10 Issue 6, p354-358. 5p.
Autor:
La Nasa, Giorgio, Littera, Roberto, Locatelli, Franco, Giardini, Claudio, Ventrella, Arianna, Mulargia, Marina, Vacca, Adriana, Orrù, Nicola, Orrù, Sandro, Piras, Eugenia, Giustolisi, Giada, Lisini, Daniela, Nesci, Sonia, Caocci, Giovanni, Carcassi, Carlo
Publikováno v:
In Biology of Blood and Marrow Transplantation 2007 13(11):1358-1368
Autor:
Sifakis Stavros, Manolakos Emmanouil, Vetro Annalisa, Kappou Dimitra, Peitsidis Panagiotis, Kontodiou Maria, Garas Antonios, Vrachnis Nikolaos, Konstandinidou Anastasia, Zuffardi Orsetta, Orru Sandro, Papoulidis Ioannis
Publikováno v:
Molecular Cytogenetics, Vol 5, Iss 1, p 12 (2012)
Abstract Wolf-Hirschhorn syndrome (WHS) is a well known genetic condition caused by a partial deletion of the short arm of chromosome 4. The great variability in the extent of the 4p deletion and the possible contribution of additional genetic rearra
Externí odkaz:
https://doaj.org/article/b560f5780c8d4f479a51e78ec5f82ace
Autor:
Eleftheriades Makarios, Tsoplou Panagiota, Vasileiadis Lefteris, Kitsos George, Garas Antonios, Louizou Eirini, Rapti Stamatia-Maria, Kefalas Konstantinos, Vetro Annalisa, Manolakos Emmanouil, Peitsidis Panagiotis, Orru Sandro, Liehr Thomas, Petersen Michael B, Thomaidis Loretta
Publikováno v:
Molecular Cytogenetics, Vol 3, Iss 1, p 22 (2010)
Abstract Background The genetic diagnosis of mental retardation (MR) is difficult to establish and at present many cases remain undiagnosed and unexplained. Standard karyotyping has been used as one of the routine techniques for the last decades. The
Externí odkaz:
https://doaj.org/article/69a8c1d1ae6847ce9d6eaa78aa91e48f
Autor:
Peitsidis Panagiotis, Thomaidis Loretta, Papoulidis Ioannis, Louizou Eirini, Kefalas Konstantinos, Neroutsou Rosita, Orru Sandro, Manolakos Emmanouil, Sotiriou Sotirios, Kitsos George, Tsoplou Panagiota, Petersen Michael B, Metaxotou Aikaterini
Publikováno v:
Molecular Cytogenetics, Vol 2, Iss 1, p 26 (2009)
Abstract Background Jacobsen syndrome (JBS) is a rare chromosomal disorder leading to multiple physical and mental impairment. This syndrome is caused by a partial deletion of chromosome 11, especially subband 11q24.1 has been proven to be involved.
Externí odkaz:
https://doaj.org/article/a11e26e40241409994a4381254d70816
Autor:
Garas Antonios, Weise Anja, Ewers Elisabeth, Kosyakova Nadezda, Kontodiou Maria, Anagnostopoulou Katerina, Lagou Magdalini, Manolakos Emmanouil, Kitsiou-Tzeli Sofia, Orru Sandro, Liehr Thomas, Metaxotou Aikaterini
Publikováno v:
Molecular Cytogenetics, Vol 2, Iss 1, p 8 (2009)
Externí odkaz:
https://doaj.org/article/752f0f94abd14369a0b74819797d42d0
Autor:
Kokotas Haris, Orru Sandro, Mihalatos Markos, Weise Anja, Neroutsou Rozita, Thomaidis Loreta, Kosyakova Nadezda, Manolakos Emmanouil, Kitsos George, Liehr Thomas, Petersen Michael B
Publikováno v:
Molecular Cytogenetics, Vol 1, Iss 1, p 24 (2008)
Abstract We report on a 7 years and 4 months old Greek boy with mild microcephaly and dysmorphic facial features. He was a sociable child with maxillary hypoplasia, epicanthal folds, upslanting palpebral fissures with long eyelashes, and hyperteloris
Externí odkaz:
https://doaj.org/article/08d8a4f01e1742afa6f3a5e7431f6a13