L. M. Kuzenkova

Selective screening and molecular characteristics of Russian patients with Pompe disease

A. Fisenko, E. Basargina, O. P. Zharova, 2021, L.O. Badalyan Neurological Journal.

[Open, non-comparative phase III clinical study to evaluate the efficacy and safety of sapropterin in patients with phenylketonuria and hyperphenylalaninemia].

O. Kovtun, T. Bushueva, M. Filimonova, 2014, Vestnik Rossiiskoi akademii meditsinskikh nauk.

Family Analysis of Linkage and Association of HLA-DRB1, CTLA4, TGFB1, IL4, CCR5, RANTES, MMP9 and TIMP1 Gene Polymorphisms with Multiple Sclerosis

M. Sudomoina, O. Favorova, O. Kulakova, 2011, Acta naturae.

Molecular characteristics of patients with glycosaminoglycan storage disorders in Russia.

A. Baranov, D. Chistiakov, L. Namazova-Baranova, 2014, Clinica chimica acta; international journal of clinical chemistry.

Genetic analysis of 17 children with Hunter syndrome: identification and functional characterization of four novel mutations in the iduronate-2-sulfatase gene.

A. Baranov, D. Chistiakov, L. Namazova-Baranova, 2014, Journal of genetics and genomics = Yi chuan xue bao.

Linkage and association of proinflammatory cytokines genes IL-6, IFNG and TNF with multiple sclerosis

M. Sudomoina, O. Favorova, O. Kulakova, 2010, Molecular Biology.

[Case of combination of Beckwith-Wiedemann syndrome with West syndrome].

T. Podkletnova, L. M. Kuzenkova, O. Globa, 2014, Vestnik Rossiiskoi akademii meditsinskikh nauk.

Assumption of heparin-induced thrombocytopenia in mucopolysaccharidoses

L. M. Kuzenkova, L. A. Osipova, 2021, Journal of Ideas in Health.

THE USE OF TOPIRAMATE FOR EPILEPSY TREATMENT IN CHILDREN

L. M. Kuzenkova, O. Globa, M. R. Kremenchugskaya, 2016 .