Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tatiana T. Batysheva"'
Autor:
Yurii S. Alexandrovich, Ekaterina I. Alekseeva, Maya D. Bakradze, Alexander A. Baranov, Tatiana T. Batysheva, Nato D. Vashakmadze, Marina G. Vershinina, Elena A. Vishneva, Anastasia A. Glazyrina, Olga B. Gordeeva, Elena Yu. Dyakonova, Еlena S. Zholobova, Dmitry V. Zabolotsky, Nadezda N. Zvereva, Irina V. Zelenkova, Dmitry O. Ivanov, Elena V. Kaytukova, George A. Karkashadze, Ivan V. Konovalov, Daria S. Kruchko, Tatiana V. Kulichenko, Seda Kh. Kurbanova, Yliya G. Levina, Yuri V. Lobzin, Ludmila N. Mazankova, Tea V. Margieva, Leyla S. Namazova-Baranova, Yulia Yu. Novikova, Dmitry Yu. Ovsyannikov, Elena E. Petryaykina, Yuriy V. Petrenko, Nataliya V. Petrova, Dmitry V. Prometnoy, Konstantin V. Pshenisov, Gregory V. Revunenkov, Alexey Yu. Rtishchev, Dina S. Rusinova, Mukhammad A. Sayfullin, Ruslan F. Sayfullin, Liliya R. Selimzyanova, Vladimir K. Tatochenko, Rustem F. Tepaev, Aleksandr N. Uskov, Marina V. Fedoseenko, Andrey P. Fisenko, Andrey V. Khar’kin, Kamilla E. Efendieva, Alexey V. Yakovlev
Publikováno v:
Pediatričeskaâ Farmakologiâ, Vol 17, Iss 3, Pp 187-212 (2020)
The Ministry of Health of the Russian Federation jointly with professional association and experts in the field of pediatrics, infectious diseases and resuscitation has revised guidelines “Clinical Features and Management of the Disease Caused by N
Autor:
Anastasiya A. Lyalina, Olga B. Kondakova, Evgeniya V. Krustaleva, Ilya V. Kanivets, Tatiana T. Batysheva, Dmitry I. Grebenkin
Publikováno v:
L.O. Badalyan Neurological Journal. 1:29-34
Background. PittHopkins syndrome (PHS) is the rare inherited disease, caused by a microdeletion on chromosome 18q21 or heterozygous mutation TCF4 gene and characterized by severe mental retardation, abnormal breathing patterns: hyperventilation, apne
Publikováno v:
Pediatrician (St. Petersburg). 7:65-72
Nowdays, cerebral palsy is a leader in the structure of chronic diseases of childhood. The earliest start of the rehabilitation of children with cerebral palsy, continuity and phasing their implementation, systematic and comprehensive, individual app