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pro vyhledávání: '"Elizaveta O. Beschastnaya"'
Autor:
Galina Yu. Poretskova, Elena A. Kalinina, Natalia N Korotkova, Olga G. Bolgarova, Natalia N. Kuznetsova, Shamil I. Gaisin, Elizaveta O. Beschastnaya
Publikováno v:
Клиническая практика, Vol 15, Iss 2, Pp 98-105 (2024)
BACKGROUND: Pyruvate dehydrogenase deficit is a severe hereditary mitochondrial metabolic disease characterized by impaired energy metabolism and manifested by a wide range of neurological symptoms. The difficulty in selecting therapy is due to insuf
Externí odkaz:
https://doaj.org/article/d599f60c7f04479eb6f7b5a404b46165