Zobrazeno 1 - 10
of 242
pro vyhledávání: '"Christodoulou Kyproula"'
Autor:
Aristos Aristodimou, Athos Antoniades, Efthimios Dardiotis, Eleni Loizidou, George Spyrou, Christina Votsi, Christodoulou Kyproula, Marios Pantzaris, Nikolaos Grigoriadis, Georgios Hadjigeorgiou, Theodoros Kyriakides, Constantinos Pattichi
Publikováno v:
IEEE Open Journal of Engineering in Medicine and Biology, Vol 2, Pp 256-262 (2021)
Goal: Most common diseases are influenced by multiple gene interactions and interactions with the environment. Performing an exhaustive search to identify such interactions is computationally expensive and needs to address the multiple testing proble
Externí odkaz:
https://doaj.org/article/37424223ba2649ab913818a0b0e64cf5
Autor:
Zamba-Papanicolaou Eleni, Middleton Lefkos T, Votsi Christina, Georghiou Anthi, Nicolaou Paschalis, Christodoulou Kyproula
Publikováno v:
BMC Medical Genetics, Vol 9, Iss 1, p 28 (2008)
Abstract Background Senataxin (chromosome 9q34) was recently identified as the causative gene for an autosomal recessive form of Ataxia (ARCA), termed as Ataxia with Oculomotor Apraxia, type 2 (AOA2) and characterized by generalized incoordination, c
Externí odkaz:
https://doaj.org/article/137c8a09e0b346f4a50ffbd419ea6980
Publikováno v:
In Computational and Structural Biotechnology Journal 2023 21:378-387
Akademický článek
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Akademický článek
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Autor:
Koutsis, Georgios, Kastritis, Efstathios, Kontogeorgiou, Zoi, Kartanou, Chrisoula, Kokotis, Panagiotis, Rentzos, Michail, Breza, Marianthi, Kleopa, Kleopas A., Christodoulou, Kyproula, Oikonomou, Evangelos, Anastasakis, Aris, Angelidakis, Panagiotis, Sarmas, Ioannis, Kargiotis, Odysseas, Tzagournissakis, Minas, Zaganas, Ioannis, Foukarakis, Emmanouil, Sachpekidis, Vasileios, Papathoma, Alexandra, Panas, Marios, Stefanis, Leonidas, Dimopoulos, Meletios Athanasios, Karadima, Georgia
Publikováno v:
In Neuromuscular Disorders December 2021 31(12):1251-1258
Autor:
Adoukonou, Thierry, Aryani, Omid, Barisic, Nina, Bashiri, Fahad, Bastaki, Laila, Benitto, Afaf, Omran, Tawfeg Ben, Bernert, Guenther, Bertini, Enrico, Borde, Patricia, Born, Peter, Boustani, Rose-Mary, Butoianu, Nina, Castiglioni, Claudia, Catibusic, Feriha, Chan, Sophelia, Chien, Yin Hsiu, Christodoulou, Kyproula, Dejsuphong, Donniphat, Farrar, Michelle, Filip, Duma, Goemans, Nathalie, Guinhouya, Kokou, Haberlova, Jana, Hadzsiev, Kinga, Hovhannesyan, Kristine, Isohanni, Pirjo, Radovic, Nelica Ivanovic, Jacquier, David, Jalloh, Alusine, Jedrzejowska, Maria, Kandawasvika, Gwen, Kaputu, Celestin, Kawatu, Nfwama, Kernohan, Kristin, Kirschner, Jan, Klink, Barbara, Kodsy, Sherry, Kouame-Assouan, Ange-Eric, Kravljanac, Ruzica, Kreile, Madara, Litvinenko, Ivan, McMillan, Hugh, Mesa, Sandra, Mohamed, Inaam, Kanzoska, Liljana Muaremoska, Nevo, Yoram, Nguefack, Seraphin, Nkole, Kafula, O'Grady, Gina, O'Rourke, Declan, Oskoui, Maryam, Piazzon, Flavia, Poddighe, Dimitri, Prasauskiene, Audrone, Prieto, Juan, Rasmussen, Magnhild, Razafindrasata, Santara, Saha, Narayan, Saito, Kayoko, Sakadi, Foksouna, Sangare, Modibo, Schroth, Mary, Shalkevich, Leanid, Shatillo, Andriy, Suthar, Renu, Szabo, Lena, Tatishvili, Nana, Tazir, Meriem, Tizzano, Eduardo, Topaloglu, Haluk, Tulinius, Mar, van der Pol, Ludo, Vazquez, Gabriel, Vlodavets, Dimitry, Wanigasinghe, Jithangi, Wilmshurst, Jo, Xiong, Hui, Zafeiriou, Dimitrios, Zamba, Eleni, Dangouloff, Tamara, Vrščaj, Eva, Servais, Laurent, Osredkar, Damjan
Publikováno v:
In Neuromuscular Disorders June 2021 31(6):574-582
Autor:
Charalambous, Despina, Christoforou, Michalis, Christou, Krystallo, Christou, Melina, Ververis, Antonis, Andreou, Marios, Christodoulou, Kyproula, Koutsoulidou, Andrie, Papachrysostomou, Christoforos, Pantelidou, Maria
Publikováno v:
Plants (2223-7747); Jul2024, Vol. 13 Issue 14, p1982, 17p
Autor:
Votsi, Christina, Tomazou, Marios, Nicolaou, Paschalis, Pantzaris, Marios C., Pitsas, Giorgos, Adamou, Archontia, Kleopa, Kleopas A., Zamba-Papanicolaou, Eleni, Christodoulou, Kyproula
Publikováno v:
Neurology: Genetics; Jun2024, Vol. 10 Issue 3, p1-10, 10p
Publikováno v:
In European Journal of Medical Genetics March 2020 63(3)