Výsledky vyhledávání - Албена Тодорова
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TSEN54 Gene-Related Pontocerebellar Hypoplasia Type 2 Could Mimic Dyskinetic Cerebral Palsy with Severe Psychomotor Retardation Autor Iliyana Pacheva, Tihomir Todorov, Иван Иванов, Desislava Tartova, Katerina Gaberova, Албена Тодорова, Diana Dimitrova
Vydáno 2018Artigo -
2
A common haplotype of the annexin A5 (ANXA5) gene promoter is associated with recurrent pregnancy loss Autor Nadia Bogdanova, Jürgen Horst, Marcin Chlystun, Peter J.P. Croucher, Almut Nebel, A. Bohring, Албена Тодорова, Stefan Schreiber, Volker Gerke, Michael Krawczak, Arseni Markoff
Vydáno 2007Artigo -
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De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome Autor Arvid Suls, Johanna A. Jaehn, Angéla Kecskés, Yvonne G. Weber, Sarah Weckhuysen, Dana Craiu, Aleksandra Siekierska, Tania Djémié, Tatiana Afrikanova, Padhraig Gormley, Sarah von Spiczak, Gerhard Kluger, Catrinel Iliescu, Tiina Talvik, Inga Talvik, Cihan Meral, Hande Çağlayan, Beatriz G. Giráldez, José M. Serratosa, Johannes R. Lemke, Dorota Hoffman‐Zacharska, Elżbieta Szczepanik, Nina Barišić, Vladimı́r Komárek, Helle Hjalgrim, Rikke S. Møller, Tarja Linnankivi, Petia Dimova, Pasquale Striano, Federico Zara, Carla Marini, Renzo Guerrini, Christel Depienne, Stéphanie Baulac, Gregor Kuhlenbäumer, Alexander D. Crawford, Anna‐Elina Lehesjoki, Peter de Witte, Aarno Palotie, Holger Lerche, Camila V. Esguerra, Peter De Jonghe, Ingo Helbig, Rik Hendrickx, Philip Holmgren, Ulrich Stephani, Hiltrud Muhle, Manuela Pendiziwiat, Silke Appenzeller, Kaja Kristine Selmer, Eva H. Brilstra, Bobby P.C. Koeleman, Felix Rosenow, Eric LeGuern, Katalin Štěrbová, Budisteanu Magdalena, Gherghiceanu Rodica, Oana Tarta Arsene, Barca Diana, Rosa Guerrero, Laura Ortega, Албена Тодорова, Andrey Kirov, Angela Robbiano, Mutluay Arslan, Uluç Yiş, Vanja Ivanović
Vydáno 2013Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Medicine
Gene
Pregnancy
Psychiatry
Alternative medicine
Annexin
Annexin A5
Cerebral palsy
Cognition
Confidence interval
Disease
Dravet syndrome
Encephalopathy
Epilepsy
Factor V Leiden
Fetus
Genotype
Haplotype
Hypoplasia
Immunology
In vitro
Internal medicine
Loss function
Microcephaly
Myoclonic epilepsy
Neuroimaging
Odds ratio
Pathology