Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yu. A. Rogozhina"'
Autor:
V. A. Rumyantseva, Yu. A. Rogozhina, A. A. Bukaeva, D. V. Bazarov, E. R. Charchyan, E. V. Zaklyazminskaya
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 7-14 (2016)
Aim. To invent a complex approach to patients with “marfanoid phenotype” undergoing surgery, applying the DNA-diagnostics of the gene FBN1 and medical genetic counseling.Material and methods. In the group of 37 patients with suspected Marfan synd
Externí odkaz:
https://doaj.org/article/71eb75d8bfa54a8a8dae90231d2625d6
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 61-64 (2015)
Aim. The development of an optimal protocol for diagnostic search for mutations with the use of the new generation sequencing technique (NGS) and evaluation of the mutation spectrum in Russian selection of the patients with Marfan syndrome.Material a
Externí odkaz:
https://doaj.org/article/24dd73f52cb24cf7ac843b239a5a8c11
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 5, Pp 55-60 (2014)
Aim. Molecular-genetic tests for neonatal type of Mrfan syndrome make possible to clarify a dignosis in children with multiple phenotype anomalies and to choose correct treatment strategy.Material and methods. Medical-genetic testing and instrumental
Externí odkaz:
https://doaj.org/article/1271ee23556a4bfc9846a96bc85d275b
Publikováno v:
Pediatric dentistry and dental prophylaxis.
Relevance. Questions of methodology and organization of specialized treatment of patients with congenital maxillofacial defects do not lose their relevance and retain the interest of researchers and practitioners. This article covers the accumulated
Autor:
O. L. Mironovich, T. A. Adyan, V. A. Rumyantseva, A. V. Polyakov, Yu. A. Rogozhina, A. N. Semyachkina
Publikováno v:
Russian Journal of Genetics. 53:809-812
Marfan syndrome (MFS) is an autosomal dominant inherited systemic disorder of connective tissue with many clinical manifestations in the cardiovascular, skeletal, and ocular systems. MFS is caused by mutations in the fibrillin-1 (FBN1) gene. To date,
Autor:
Elena Zaklyazminskaya, D. G. Breshenkov, D. N. Fedorov, Yu. A. Rogozhina, E. R. Charchyan, Stepanenko Ab, V. A. Rumyantseva
Publikováno v:
Kardiologiya i serdechno-sosudistaya khirurgiya. 10:79
Publikováno v:
ResearcherID
Российский кардиологический журнал, Vol 0, Iss 5, Pp 55-60 (2014)
Scopus-Elsevier
Российский кардиологический журнал, Vol 0, Iss 5, Pp 55-60 (2014)
Scopus-Elsevier
Aim. Molecular-genetic tests for neonatal type of Mrfan syndrome make possible to clarify a dignosis in children with multiple phenotype anomalies and to choose correct treatment strategy. Material and methods. Medical-genetic testing and instrumenta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74f3c42117b6ef51673236deb91d67d7
http://www.scopus.com/inward/record.url?eid=2-s2.0-84932618367&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84932618367&partnerID=MN8TOARS