A. K. Gevorkyan

Critical clinical situations in adult patients with Mucopolysaccharidoses (MPS)

C. Hendriksz, K. Stepien, C. Lampe, 2020, Orphanet Journal of Rare Diseases.

Critical clinical situations in adult patients with Mucopolysaccharidoses (MPS)

C. Hendriksz, M. Riera, K. Stepien, 2019, Orphanet Journal of Rare Diseases.

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.

FEATURES OF DIAGNOSIS OF BILIARY ATRESIA IN CHILDREN

I. E. Smirnov, G. V. Volynets, A. S. Potapov, 2019, Russian Pediatric Journal.

Step by step diagnosis of hereditary tyrosinemia type I in children

I. E. Smirnov, L. Namazova-Baranova, G. V. Volynets, 2019, Russian Pediatric Journal.