In vitro biotization by M I Yablonskaya, M S Gins, M A Molchanova

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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

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Immune-mediated epilepsies in children by E. D. Belousova, M. I. Yablonskaya, M. K. Tagirova, S. L. Kulikova, S. A. Likhachev

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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

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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

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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

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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

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