Zobrazeno 1 - 10
of 151
pro vyhledávání: '"Maria, Tzetis"'
Autor:
Lamprini Nasi, Alexios Alexopoulos, Eleftheria Kokkinou, Kleoniki Roka, Maria Tzetis, Maria Tsipi, Talia Kakourou, Christina Kanaka-Gantenbein, George Chrousos, Antonis Kattamis, Roser Pons
Publikováno v:
Acta Dermato-Venereologica, Vol 103 (2023)
Cafe-au-lait macules are the most distinctive clinical finding in neurofibromatosis type I. The aim of this prospective study of Greek children diagnosed with neurofibromatosis type I was to describe the dermatological phenotype and to analyse the ch
Externí odkaz:
https://doaj.org/article/09f52d42d3be471aba1fba0d8682fec1
Autor:
Evangelia Tzeravini, Stamatia Samara, Anna Kouramba, Georgios Vakrinos, Athina Efthimiou, Maria Tzetis, Theodoros Androutsakos
Publikováno v:
Case Reports in Neurology, Vol 14, Iss 2, Pp 261-267 (2022)
Severe hemophilia A and moyamoya (SHAM) syndrome is a rare condition that combines hemophilia A and moyamoya disease (MMD) due to an Xq28 microdeletion encompassing the F8 and BRCC3 genes. Here, we report the case of a 19-year-old male patient with h
Externí odkaz:
https://doaj.org/article/79cf2441d6304cbab2a709f3259cc9ee
Autor:
Vasileios Konteles, Ioanna Papathanasiou, Maria Tzetis, Evgenios Goussetis, Varvara Trachana, Evanthia Mourmoura, Charalampos Balis, Konstantinos Malizos, Aspasia Tsezou
Publikováno v:
Cells, Vol 12, Iss 13, p 1756 (2023)
Although MSCs grant pronounced potential for cell therapies, several factors, such as their heterogeneity restrict their use. To overcome these limitations, iMSCs (MSCs derived from induced pluripotent stem cells (iPSCs) have attracted attention. Her
Externí odkaz:
https://doaj.org/article/52cee0befc4d4852a2cdca7f8fa51485
Autor:
Panagiotis Ntostis, Grace Swanson, Georgia Kokkali, David Iles, John Huntriss, Agni Pantou, Maria Tzetis, Konstantinos Pantos, Helen M. Picton, Stephen A. Krawetz, David Miller
Publikováno v:
iScience, Vol 24, Iss 7, Pp 102751- (2021)
Summary: Advancing age has a negative impact on female fertility. As implantation rates decline during the normal maternal life course, age-related, embryonic factors are altered and our inability to monitor these factors in an unbiased genome-wide m
Externí odkaz:
https://doaj.org/article/9598239f80f749fbae8b1abef1b8e1a7
Autor:
Panagiotis Ntostis, Grace Swanson, Georgia Kokkali, David Iles, John Huntriss, Agni Pantou, Maria Tzetis, Konstantinos Pantos, Helen M. Picton, Stephen A. Krawetz, David Miller
Publikováno v:
Systems Biology in Reproductive Medicine. 69:3-19
Increasing female age is accompanied by a corresponding fall in her fertility. This decline is influenced by a variety of factors over an individual's life course including background genetics, local environment and diet. Studying both coding and non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08166166d2512dfe1a64673f35574dc0
https://doi.org/10.1080/19396368.2022.2153636
https://doi.org/10.1080/19396368.2022.2153636
Autor:
Tsezou, Vasileios Konteles, Ioanna Papathanasiou, Maria Tzetis, Evgenios Goussetis, Varvara Trachana, Evanthia Mourmoura, Charalampos Balis, Konstantinos Malizos, Aspasia
Publikováno v:
Cells; Volume 12; Issue 13; Pages: 1756
Although MSCs grant pronounced potential for cell therapies, several factors, such as their heterogeneity restrict their use. To overcome these limitations, iMSCs (MSCs derived from induced pluripotent stem cells (iPSCs) have attracted attention. Her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::7cd53f2a970bbda326d625228b2719b5
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:
Danai Veltra, Faidon-Nikolaos Tilemis, Nikolaos M. Marinakis, Maria Svingou, Anastasios Mitrakos, Konstantina Kosma, Irene Tsoutsou, Periklis Makrythanasis, Virginia Theodorou, Marina Katsalouli, Pelagia Vorgia, Georgios Niotakis, Georgios Vartzelis, Argirios Dinopoulos, Athanasios Evangeliou, Stella Mouskou, Anastasia Korona, Sotiria Mastroyianni, Antigone Papavasiliou, Maria Tzetis, Roser Pons, Joanne Traeger-Synodinos, Christalena Sofocleous
Genetics of epilepsy are highly heterogeneous and complex. Lesions detected involve genes encoding various types of channels, transcription factors, and other proteins implicated in numerous cellular processes, such as synaptogenesis. Consequently, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95c7e76871eca36a992422ab57cba7f9
Autor:
Menelaos Kanakis, Filia Diamantea, Maria Tzetis, Chrysanthi Koutsandrea, Dimitrios Papaconstantinou, Panagiotis Giannakouras, Ilias Georgalas
Publikováno v:
European Journal of Ophthalmology. 32:976-983
Introduction: Cystic fibrosis (CF) is the most common life-shortening recessive genetic disease in Caucasians, affecting primarily the lungs. The objective of our study was to investigate potential ophthalmologic involvement in adult patients with CF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9055653bd91e07fb8252db7ba71697f9
https://doi.org/10.1177/11206721211008780
https://doi.org/10.1177/11206721211008780
Autor:
Anastasios Mitrakos, Maria Tsipi, Joanne Traeger-Synodinos, Maria Tzetis, Konstantinos Varvagiannis, Konstantina Kosma
Publikováno v:
Molecular Syndromology. 12:321-326
Pathogenic KMT2E variants underly O'Donnell-Luria-Rodan syndrome, a recently described neurodevelopmental disorder characterized by global developmental delay, variable degrees of intellectual disability, and subtle facial dysmorphism. Less common fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85b96524f5a75ae34b930305cb36938d
https://doi.org/10.1159/000516635
https://doi.org/10.1159/000516635