Maria Alexandrovna Shkolnikova

5PUBLICATIONS
6CO-AUTHORS
Medical biochemistry - proteins and peptides (incl. medical proteomics)Developmental genetics (incl. sex determination)Aboriginal and Torres Strait Islander and disabilitySolid state chemistry
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Publications (5)

|Mar 12, 2026
A cross-sectional observational study: assessment of cardiovascular damage in mucopolysaccharidoses mutation carriers.

Thanh Luan Nguyen, Alla Nikolaevna Semyachkina, Victoria Yurievna Voinova

|Sep 10, 2021
Ehlers-Danlos syndrome kyphoscoliotic type 2 caused by mutations in the FKBP14 gene: an analysis of five cases.

Alla Nikolaevna Semyachkina, Ekaterina Alexandrovna Nikolaeva, Nailya Mansurovna Galeeva

|Mar 07, 2021
Analysis of long-term observations of the large group of Russian patients with Hunter syndrome (mucopolysaccharidosis type II).

Alla Nikolaevna Semyachkina, Elena Yurievna Voskoboeva, Ekaterina Alexandrovna Nikolaeva

|May 04, 2019
Case report: a rare case of Hunter syndrome (type II mucopolysaccharidosis) in a girl.

A N Semyachkina, E Y Voskoboeva, E Y Zakharova

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