In vitro biotization

by M I Yablonskaya, M S Gins, M A Molchanova
Published 2016-12-01

Polymorphism of the clinical manifestations of progressive mitochondrial encephalomyopathy associated with POLG1 gene mutation

by M. I. Yablonskaya, E. A. Nikolaeva, P. A. Shatalov, M. N. Kharabadze
Published 2016-07-01

Immune-mediated epilepsies in children

by E. D. Belousova, M. I. Yablonskaya, M. K. Tagirova, S. L. Kulikova, S. A. Likhachev
Published 2016-03-01

Specific features of the clinical and laboratory diagnosis of Lesch—Nyhan syndrome and current therapy options

by M. I. Yablonskaya, P. V. Novikov, E. G. Agapov, I. V. Zolkina, E. A. Yuryeva, M. N. Kharabadze
Published 2016-03-01

Biopterin-deficient hyperphenylalaninemia: Diagnosis and treatment

by E. A. Nikolaeva, M. I. Yablonskaya, M. N. Kharabadze, Yu. I. Davydova, O. N. Komarova, P. V. Novikov
Published 2016-03-01

IXa glycogenosis – diagnosis, features of clinical manifestations and treatment

by M. I. Yablonskaya, E. A. Nikolayeva, A. N. Semyachkina, O. N. Komarova, M. L. Babayan, M. N. Kharabadze, Yu. I. Davydova, A. R. Zabrodina
Published 2018-04-01

Glycogen storage disease type II (Pompe disease) in children

by A. N. Semyachkina, V. S. Sukhorukov, T. M. Bukina, M. I. Yablonskaya, E. S. Merkuryeva, M. N. Kharabadze, E. A. Proskurina, E. Yu. Zakharova, A. V. Brydun, P. A. Shatalov, P. V. Novikov
Published 2016-03-01