Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Katerina Anagnostopoulou"'
Autor:
Genovefa Kolovou, Christina Marvaki, Stamatis Makrygiannis, Olga Kadda, Vasiliki Giannakopoulou, Petros Kalogeropoulos, Katerina Anagnostopoulou, Georgios Goumas, Georgios Kazianis, Sotiria Limberi, Despina Perrea, Vana Kolovou, Helen Bilianou
Publikováno v:
Hellenic Journal of Cardiology, Vol 61, Iss 4, Pp 284-287 (2020)
Externí odkaz:
https://doaj.org/article/fcd2242f1ea7410fbce1c3407376b76b
Autor:
Petros Kalogeropoulos, Olga Kadda, Georgios Kazianis, Helen Bilianou, Katerina Anagnostopoulou, Despina Perrea, Vasiliki Giannakopoulou, Georgios Goumas, Genovefa Kolovou, Vana Kolovou, Christina Marvaki, Sotiria Limberi, Stamatis Makrygiannis
Publikováno v:
Hellenic Journal of Cardiology, Vol 61, Iss 4, Pp 284-287 (2020)
Autor:
Maria Banti, Ioannis A. Sfontouris, Harris Kontos, T.G. Lainas, George T. Lainas, Efthimios Faros, Katerina Anagnostopoulou, George K. Petsas, Efstratios M. Kolibianakis, Katerina Kardara
Publikováno v:
Systems Biology in Reproductive Medicine. 64:283-290
The presence of smooth endoplasmic reticulum aggregates (SERa) in the ooplasm is considered as the most severe oocyte dysmorphism due to its serious and potentially lethal outcomes in offspring. In the present case report, a couple underwent their fi
Autor:
Roser Pons, Christalena Sofocleus, Belén Pérez-Dueñas, Danae Veltra, Katerina Anagnostopoulou, Vasiliki Zouvelou, Helen Fryssira, Rafael Artuch, Elissavet Kollia, Anna Marcé-Grau, Manolis Bilanakis, Xaralabos Kokkinis, Loukia Apostolakopoulou, Filippo M. Santorelli, Judith Amstrong, Kiriaki Kekou, Rosa J. Torres, Eleftheria Kokkinou, Delia Yubero, Antonis Voutetakis, Ioannis Nikas, Zoi Dalivigka, Alfons Macaya
Publikováno v:
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Objective: Non-progressive genetic disorders may present with motor dysfunction resembling cerebral palsy (CP). Such patients are often characterized as CP mimics. The purpose of this work was to delineate the clinical manifestations and molecular fi
Autor:
Kolovou, Genovefa D.1 genovefa@kolovou.com, Katerina, Anagnostopoulou1, Ioannis, Vasiliadis1, Cokkinos, Dennis V.1
Publikováno v:
Cardiovascular Therapeutics. Summer2008, Vol. 26 Issue 2, p166-178. 13p. 1 Diagram.
Autor:
Sofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, Katerina Anagnostopoulou, Maria Kontodiou, Nadezda Kosyakova, Elisabeth Ewers, Anja Weise, Antonios Garas, Sandro Orru, Thomas Liehr, Aikaterini Metaxotou
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 2, Iss 1, p 8 (2009)
Molecular Cytogenetics, Vol 2, Iss 1, p 8 (2009)
The heterogeneous group of small supernumerary marker chromosomes (sSMCs) presents serious counseling problems, especially if they are present de novo and diagnosed prenatally. The incidence has been estimated at 1 in 1000 prenatal samples. We presen