Zobrazeno 1 - 10
of 206
pro vyhledávání: '"Emmanuel, Kanavakis"'
Autor:
Elisavet Kouvidi, Hara Tsimela, Leandros Lazaros, Kalliopi N Manola, Sophia Zachaki, Ruxandra Dobrescu, Konstantinos Sfakianoudis, Theodora Tsoni, Christina Katsidi, Haralambia Tsarouha, Emmanuel Kanavakis, Ariadni Mavrou
Publikováno v:
Journal of Human Reproductive Sciences, Vol 15, Iss 3, Pp 307-317 (2022)
46,XX male sex reversal syndrome is a rare genetic cause of male infertility. We report on two new cases of this syndrome in men presenting with hypogonadism and infertility. Cytogenetic and molecular analysis was performed in both patients. An exten
Externí odkaz:
https://doaj.org/article/a6a515c629cd4f0597776ef60a30578d
Autor:
Amelia Pantou, Anastasios Mitrakos, Georgia Kokkali, Konstantina Petroutsou, Georgia Tounta, Leandros Lazaros, Alexandros Dimopoulos, Konstantinos Sfakianoudis, Konstantinos Pantos, Michael Koutsilieris, Ariadni Mavrou, Emmanuel Kanavakis, Maria Tzetis
Publikováno v:
J Assist Reprod Genet
PURPOSE: To investigate whether preimplantation genetic testing for aneuploidy (PGT-A) improves the clinical outcome in patients with advanced maternal age (AMA), recurrent miscarriages (RM), and recurrent implantation failure (RIF). METHODS: Retrosp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94c13db1157aa92c2540d078bd2890c7
https://doi.org/10.1007/s10815-022-02461-9
https://doi.org/10.1007/s10815-022-02461-9
Autor:
Stefanos Syrkos, Birgit Panopoulou, Emmanuel Kanavakis, Emmanuel Promponas, Sophia Zachaki, Amelia Pantou, Kalliopi N. Manola, Elisavet Kouvidi, Ariadni Mavrou, Marina Kalomoiraki
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 264:212-218
Objective To determine chromosome and gene alterations in ectopic endometrial (EM) tissue which may be implicated in the clinical course or the progression of endometriosis and to review the literature concerning the cytogenetic findings of women wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1930064d4b2e2774b856fc03f2384217
https://doi.org/10.1016/j.ejogrb.2021.07.028
https://doi.org/10.1016/j.ejogrb.2021.07.028
Autor:
Elisavet Kouvidi, Sophia Zachaki, Haralampia Tsarouha, Amelia Pantou, Kalliopi N. Manola, Emmanuel Kanavakis, Ariadni Mavrou
Publikováno v:
Cytogenetic and Genome Research. 161:551-555
Chromosomal abnormalities are often detected in women with reproductive problems. This study aimed to investigate the presence and type of chromosomal aberrations in peripheral blood of women undergoing in vitro fertilization (IVF) and their possible
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2888812cec54cfb1c8e5a9c8ae6db6e
https://doi.org/10.1159/000521655
https://doi.org/10.1159/000521655
Autor:
Ariadni Mavrou, Leandros Lazaros, Emmanuel Kanavakis, Maria Tzetis, Anastasios Mitrakos, Amelia Pantou
Publikováno v:
Molecular Syndromology. 11:141-145
Coffin-Siris Syndrome 4 is an autosomal dominant congenital malformation syndrome caused by heterozygous mutations in the SMARCA4 gene with its main features being intellectual disability, developmental delay, behavioral abnormalities, and hypoplasti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::306ff8f329579cd98b24770ccd7d267d
https://doi.org/10.1159/000508563
https://doi.org/10.1159/000508563
Autor:
Emmanuel Kanavakis, Ariadni Mavrou, Amelia Pantou, Haroula Tsarouha, Anastasios Mitrakos, Kalliopi N. Manola, Ioanna Charalampous, Sophia Zachaki, Georgia Tounta, Elisavet Kouvidi
Publikováno v:
In Vivo
Background/aim To determine the incidence of X chromosome mosaicism in women undergoing in vitro fertilization (IVF) treatment and present preimplantation genetic testing for aneuploidy (PGT-A) outcome of this group. Patients and methods A total of 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3139abfca25f242e50f6a97121e97d0
https://doi.org/10.21873/invivo.11925
https://doi.org/10.21873/invivo.11925
Autor:
Irene, Sfougataki, Ioanna, Varela, Kalliope, Stefanaki, Angeliki, Karagiannidou, Maria G, Roubelakis, Vasiliki, Kalodimou, Ioanna, Papathanasiou, Joanne, Traeger-Synodinos, Sofia, Kitsiou-Tzeli, Emmanuel, Kanavakis, Vasiliki, Kitra, Aspasia, Tsezou, Maria, Tzetis, Evgenios, Goussetis
Publikováno v:
Histology and histopathology. 35(12)
Mesenchymal stromal cells (MSCs) can be derived from a wide range of fetal and adult sources including pluripotent stem cells (PSCs). The properties of PSC-derived MSCs need to be fully characterized, in order to evaluate the feasibility of their use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3ad78d4c7f0907367de6536ba68c28c5
https://pubmed.ncbi.nlm.nih.gov/32959885
https://pubmed.ncbi.nlm.nih.gov/32959885
Autor:
Marion Phylipsen, Antonio Amato, Maria Pia Cappabianca, Jan Traeger-Synodinos, Emmanuel Kanavakis, Nazli Basak, Renzo Galanello, Teresa Tuveri, Giovanni Ivaldi, Cornelis L. Harteveld, Piero C. Giordano
Publikováno v:
Haematologica, Vol 94, Iss 9 (2009)
When the molecular background of couples requesting prevention is unclear, family analysis and tools to define rare mutations are essential. We report two novel deletion defects observed in an Italian and in a Turkish couple. The first proband presen
Externí odkaz:
https://doaj.org/article/0f581e0f502d4558af91f654eca4b2f0
Autor:
Lena Maragoudaki, Cathy A. J. Bosch, Christina Vrettou, Claudia A. L. Ruivenkamp, Mariëtte J.V. Hoffer, Christos Kattamis, Janos Apostolidis, Sandra G.J. Arkesteijn, Emmanuel Kanavakis, Joanne Traeger-Synodinos, Cornelis L. Harteveld
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d434323921ec3b3c2c8e03acf81ec5b
http://hdl.handle.net/1887/121744
http://hdl.handle.net/1887/121744
Autor:
Despina Perrea, Emmanuel Kanavakis, Anny Mertzanian, Argyro Kagia, Angeliki Karagiannidou, Irene Sfougataki, Aikaterini Dimopoulou, Ioanna Varela, Maria Tzetis, Evgenios Goussetis
Publikováno v:
Inflammation. 42(5)
Acute inflammatory bowel disease (AIBD) is a wide clinical entity including severe gastrointestinal pathologies with common histopathological basis. Epidemiologically increasing diseases, such as necrotizing enterocolitis (NEC), gastrointestinal graf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dbdbae46ea8ea287bb8cfee6e2832ff
https://pubmed.ncbi.nlm.nih.gov/31227956
https://pubmed.ncbi.nlm.nih.gov/31227956