Zobrazeno 1 - 10
of 19
pro vyhledávání: '"N P, Kotlukova"'
Autor:
N. P. Kotlukova, T. S. Belysheva, L. I. Shats, V. A. Fochenkova, E. D. Chavpetsova, M. B. Belogurova, Yu. K. Toshina, Yu. V. Dinikina, I. N. Nurmeev, A. S. Seregin, A. A. Mylnikov, I. A. Mylnikov, S. M. Sokurova, O. A. Monakhova, A. A. Ivchenko, L. V. Zhivova
Publikováno v:
Russian Journal of Pediatric Hematology and Oncology. 9:22-28
Introduction. Infantile hemangiomas (IH) are the most common benign vascular tumor of children of the first year and are an interdisciplinary problem of neonatologists, pediatricians, pediatric cardiologists, oncologists, pediatric surgeons, dermatol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cee39e1961d1bebcf179314a302d8d1
https://doi.org/10.21682/2311-1267-2022-9-2-22-28
https://doi.org/10.21682/2311-1267-2022-9-2-22-28
Autor:
I. N. Zakharova, N. P. Kotlukova, V. V. Roginsky, J. J. Sokolov, O. V. Zaitseva, I. D. Maykova, G. R. Idrisova, I. I. Pshenichnikova
Publikováno v:
Медицинский совет, Vol 0, Iss 16, Pp 32-37 (2016)
Infantile hemangiomas are the most common vascular lesions newborns and infants have and they are sure to be a socially significant problem. Despite the fact that modern research techniques allow you the problems of diagnosis methods, classification,
Externí odkaz:
https://doaj.org/article/d0cf64c16f9d4afca03acd4cde8f8586
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 93-97 (2016)
Noonan syndrome is clinically and genetically heterogenic disease caused by mutations in genes coding the proteins of universal cascade of cellular signalling Ras-MAPK. Recently, about 10 genes known, with mutations leading to the disease development
Externí odkaz:
https://doaj.org/article/a1bc6f9222834de1a3a1915f07793da9
Autor:
S. S. Nikitin, S. I. Kutsev, E. N. Basargina, S. V. Mikhaylova, E. Yu. Zakharova, V. I. Larionova, S. I. Polyakova, N. P. Kotlukova, E. N. Arkhipova, M. O. Kovalchuk, N. V. Buchinskaya
Publikováno v:
Нервно-мышечные болезни, Vol 6, Iss 1, Pp 11-43 (2016)
Externí odkaz:
https://doaj.org/article/e0cae3a787574e14abdbd6b1dc15e6db
Publikováno v:
Нервно-мышечные болезни, Vol 0, Iss 4, Pp 66-73 (2015)
Pompe disease is a rare inherited disease that belongs to lysosomal accumulation diseases and can be considered as cardiac glycogenosistype II, as well as a severe neuromuscular disease or metabolic myopathy. Physicians of different specialties very
Externí odkaz:
https://doaj.org/article/1e0ddf8e31674f389330590e91d7cfef
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:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 64, Iss 2, Pp 13-21 (2019)
The article analyzes the literature on the development of views on the definition, approaches to diagnostics and tactical measures in case of suddenly manifesting conditions in children of the first year of life, accompanied by respiratory failure, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6923a58c72bfaec726d0d0b8631424de
https://www.ped-perinatology.ru/jour/article/view/851
https://www.ped-perinatology.ru/jour/article/view/851
Publikováno v:
Pediatria. Journal named after G.N. Speransky. 96:15-21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8533bd3d2379be71326774f93f2d77fc
https://doi.org/10.24110/0031-403x-2017-96-3-15-21
https://doi.org/10.24110/0031-403x-2017-96-3-15-21
Publikováno v:
Stomatologiya. 100:30
The article analyzes the results of treatment of children affected with lesions of blood vessels of the head and neck. The research is aimed at developing and implementing minimally invasive techniques to treat such children.The study group comprised
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8813d07b59a022ac949a99e92aac44f0
https://doi.org/10.17116/stomat202110005130
https://doi.org/10.17116/stomat202110005130
Autor:
Iu O, Kozlova, V V, Zabnenkova, N V, Shilova, M E, Min'zhenkova, V G, Antonenko, N P, Kotlukova, L V, Simonova, I A, Kazanceva, E G, Levchenko, T D, Bombardirova, T V, Zolotukhina, A V, Poliakov
Publikováno v:
Genetika. 50(5)
In a group of 140 patients with typical phenotype, the 22q11.2 microdeletion was detected in 43 patients (32%) using FISH and MLPA methods. There were no deletions of other chromosomal loci leading to phenotypes similar to the 22q11.2 deletion syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a7bdaed300a070ee8ec272f8d717dc8c
https://pubmed.ncbi.nlm.nih.gov/25715476
https://pubmed.ncbi.nlm.nih.gov/25715476