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pro vyhledávání: '"E Simeonov"'
Akademický článek
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Autor:
E. Simeonov, R. Madzharova
Publikováno v:
EurasianUnionScientists. 2:4-7
Purpose: Capsulitis adhesive is a degenerative disease of soft tissues around the shoulder joint. Characterized by pain and limited movements in the shoulder joint. It has always been considered important because of the impact on the quality-of-life
Autor:
Albena Jordanova, Vanyo Mitev, Maria Bojidarova, Valentina Peycheva, Elena Rodopska, E Simeonov, N Ivanova, Petia Dimova, Dimitar Stamatov, Iliana Pacheva, Daniela Deneva, Margarita V. Panova, Veneta Bojinova, D. Hristova, Ivan Litvinenko, Iliyana Aleksandrova, Elena Slavkova, Kunka Kamenarova, Radka Kaneva, Ivan Ivanov, Genoveva Tacheva
Publikováno v:
Turkish journal of pediatrics
Background. Dravet syndrome (DS) is the most severe form of Generalized Epilepsy with Febrile Seizures plus (GEFS+) syndrome with a clear genetic component in 85% of the cases. It is characterized by fever-provoked seizure onset around six months of
Autor:
Julie M. Phipps, Jenny Morton, Elizabeth Sweeney, Araceli Cuellar, Jeremy A. Sabourin, Assen Bussarsky, Val C. Sheffield, James L. Mills, Michael L. Cunningham, David W. Johnson, Karen Crawford, Krithi Bala, Mary M. Jenkins, Marta Barba, Louise C. Wilson, Cristina M. Justice, Nadezhda Yaneva, Lawrence C. Brody, Simeon A. Boyadjiev, Paul A. Romitti, Katie E. M. Rees, Andrew O.M. Wilkie, Wanda Lattanzi, Peter H. Langlois, Peter Noons, Yan Zhou, Rachel K. Tittle, Steven A. Wall, Tony Roscioli, Marike Zwienenberg, Denise M. Kay, Deirdre Cilliers, Kiril Georgiev, Jo C. Byren, Robert J. Sicko, Craig W. Senders, Lorenzo D. Botto, Alexander F. Wilson, Radka Kaneva, E Simeonov, Astrid Weber, Gianpiero Tamburrini, Kristin M Conway, James E. Boggan, Janine M. LaSalle
Publikováno v:
Hum Genet
Human Genetics, vol 139, iss 8
Human Genetics, vol 139, iss 8
Our previous genome-wide association study (GWAS) for sagittal nonsyndromic craniosynostosis (sNCS) provided important insights into the genetics of midline CS. In this study, we performed a GWAS for a second midline NCS, metopic NCS (mNCS), using 21
Publikováno v:
Trakia Journal of Science. 14:344-347
Autor:
Daniela Avdjieva-Tzavella, Dimitar Stamatov, Sashka Zhelyazkova, Radka Kaneva, Iliana A Alexandrova, Iliana Pacheva, Ivan Litvinenko, Vanyo Mitev, E Simeonov, Veneta Bozhinova, Valentina Peycheva, Kunka Kamenarova, Neviana Ivanova, Petya Dimova, Ivan Ivanov, Ivailo Tournev, Albena Jordanova
Publikováno v:
Gene
High resolution chromosomal microarray analysis (CMA) has facilitated the identification of small chromosomal rearrangements throughout the genome, associated with various neurodevelopmental phenotypes, including ID/DD. Recently, it became evident th
Autor:
E. Simeonov, V. Koleva
Publikováno v:
Chemical and Biochemical Engineering Quarterly Journal. 28:545-551
Extraction kinetics of polyphenols and flavonoids from plant material and their separation and concentration by nanofiltration were investigated. The kinetics experiments were carried out with Cotinus coggygria. The influence of the extraction solven
Akademický článek
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Autor:
Daniela Avdjieva-Tzavella, Draga Toncheva, E Simeonov, Savina Hadjidekova, Blaga Rukova, Desislava Nesheva, Dimitrina Hristova-Naydenova, Ivan Litvinenko, Radka Tincheva
Publikováno v:
Biotechnology & Biotechnological Equipment. 26:3389-3393
Autism spectrum disorders (ASDs) constitute a group of behaviorally-defined conditions whose main features are qualitative changes in social interactions, defect in communication abilities, and repetitive and stereotyped interests and activities. ASD
Autor:
Hilde Van Esch, Boyan Dimitrov, Koen Devriendt, I Bradinova, Maryse De Smedt, E Baten, Philippe Debeer, E Simeonov, Jean-Pierre Fryns, Joris Vermeesch, Thomy de Ravel, Irina Balikova
Publikováno v:
Journal of Medical Genetics. 48:98-104
Introduction The clinical phenotype of the chromosome 2q31 deletion syndrome consists of limb anomalies ranging from monodactylous ectrodactyly, brachydactyly and syndactyly to camptodactyly. Additional internal organ anomalies—for example, heart d