Olga Shchagina

Characteristics of patients with primary ciliary dyskinesia

E.D. Nikolaeva, D.Yu. Ovsyannikov, V.A. Strelnikova et al. · PULMONOLOGIYA · 2023 · 20 citations · Full text

Rare Diseases, Cilia Motor Activity, Clinical Finding +9

Ataxia with Oculomotor Apraxia Type 4 with PNKP Common “Portuguese” and Novel Mutations in Two Belarusian Families

G. E. Rudenskaya, Andrey V. Marakhonov, Olga Shchagina et al. · Journal of Pediatric Genetics · 2019 · 19 citations · Full text

HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients

Olga Shchagina, Aysylu Murtazina, G. N. Rudenskaya et al. · Molecular Biology Reports · 2019 · 19 citations

Rare Diseases, Mendelian Disorder, Recessive Hereditary Motor +12

<scp><i>GABRA1</i></scp>‐Related Disorders: From Genetic to Functional Pathways

Elisa Musto, Vivian W. Y. Liao, Katrine M. Johannesen et al. · Annals of Neurology · 2023 · 16 citations · Full text

Advanced neonatal screening for hereditary diseases in Russia: first results and future prospects

S.V. Voronin, Ekaterina Zakharova, Galina Baydakova et al. · PEDIATRIA Journal named after G N SPERANSKY · 2024 · 16 citations

Family Medicine, Neonatology, Genetic Epidemiology +23