Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Leila A. Gandaeva"'
Autor:
Olga V. Kulikova, Roman P. Myasnikov, Elena A. Mershina, Polina S. Pilus, Sergei N. Koretskiy, Aleksei N. Meshkov, Anna V. Kiseleva, Mariia S. Kharlap, Valentin E. Sinitsyn, Nataliia A. Sdvigova, Leila A. Gandaeva, Vladimir I. Barskiy, Yuliia V. Derevnina, Olga P. Zharova, Elena N. Basargina, Sergey A. Boytsov, Oksana M. Drapkina
Publikováno v:
Терапевтический архив, Vol 93, Iss 4, Pp 381-388 (2021)
Aim. To analyze and demonstrate various phenotypes in patients with familial left ventricular noncompaction (LVNC). Materials and methods. In 2013 was created a multicenter registry of LVNC patients. On its basis 30 families with a familial LVNC w
Externí odkaz:
https://doaj.org/article/48bd70e002424e6fb802d25d3a8f2b88
Autor:
Kirill V. Savostyanov, Alexander A. Pushkov, Elena N. Basargina, Lyudmila M. Kuzenkova, Natalia N. Mazanova, Leila A. Gandaeva, Olga P. Zharova, Ekaterina E. Ryabova, Ilya S. Zhanin, Andrey P. Fisenko
Publikováno v:
L.O. Badalyan Neurological Journal. 2:203-215
Introduction. Pompe disease (PD) or type II glycogenosis is a rare multisystem hereditary accumulation disease caused by a deficiency of the enzyme acid maltase (acid alpha-1,4-glucosidase), which leads to reduced activity to the accumulation of glyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef307812f6daef7acf817608b204858a
https://doi.org/10.46563/2686-8997-2021-2-4-203-215
https://doi.org/10.46563/2686-8997-2021-2-4-203-215