SEVERE EPILEPTIC ENCEPHALOPATHY OF EARLY CHILDHOOD DUE TO SCN2A MUTATION

by I. S. Bachtin, E. D. Belousova, P. A. Shatalov, S. O. Ayvazyan
Published 2016-05-01

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

Challenges Faced by Clinicians in the Personalized Treatment Planning: A Literature Review and the First Results of the Russian National Cancer Program

by P. V. Shegai, P. A. Shatalov, A. A. Zabolotneva, N. A. Falaleeva, S. A. Ivanov, A. D. Kaprin
Published 2021-01-01

Adaptational role of mitochondrial changes in congenital central core myopathy: new proofs

by I. S. Vinogradskaya, V. S. Sukhorukov, D. A. Kharlamov, T. I. Baranich, P. A. Shatalov, A. V. Brydun, T. G. Kuznetsova, V. V. Glinkina
Published 2016-03-01

Clinical and genetic characteristics of patients with type 2 early infantile epileptic encephalopathy caused by CDKL5 gene mutations

by E. L. Dadali, I. A. Akimova, F. A. Konovalov, P. A. Shatalov, A. Yu. Krasnenko, V. V. Strelnikov, M. A. Ampleeva
Published 2020-01-01

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

Limb-girdle muscular dystrophy type 2A (calpainopathy)

by T. I. Baranich, S. B. Artemyeva, N. V. Kleimenova, L. A. Khavkhun, D. V. VIodavets, D. O. Kazakov, P. A. Shatalov, E. B. Litvinova, I. V. Shulyakova, A. V. Brydun, V. V. Glinkina, V. S. Sukhorukov
Published 2016-03-01