Clinical Presentation of a Patient with a Congenital Disorder of Glycosylation, Type IIs (ATP6AP1), and Liver Transplantation

por Semenova, Natalia, Shatokhina, Olga, Shchagina, Olga, Kamenec, Elena, Marakhonov, Andrey, Degtyareva, Anna, Taran, Natalia, Strokova, Tatiana
Publicado 2023

The effect of colloidal solution of molybdenum nanoparticles on the microbial composition in rhizosphere of Cicer arietinum L.

por Taran, Natalia Yu, Gonchar, Olena M, Lopatko, Kostyantyn G, Batsmanova, Lyudmila M, Patyka, Mykola V, Volkogon, Mykola V
Publicado 2014

A novel mutation in the PEX26 gene in a family from Dagestan with members affected by Zellweger spectrum disorder

por Semenova, Natalia A., Kurkina, Marina V., Marakhonov, Andrey V., Dadali, Elena L., Taran, Natalia N., Strokova, Tatyana V.
Publicado 2021

Hyperammonemia in Russia Due to Carbonic Anhydrase VA Deficiency Caused by Homozygous Mutation p.Lys185Lys (c.555G>A) of the CA5A Gene

por Semenova, Natalia, Marakhonov, Andrey, Ampleeva, Maria, Kurkina, Marina, Baydakova, Galina, Skoblov, Mikhail, Taran, Natalia, Babak, Olga, Shchukina, Ekaterina, Strokova, Tatyana
Publicado 2022

Clinical Characterization of Alagille Syndrome in Patients with Cholestatic Liver Disease

por Semenova, Natalia, Kamenets, Elena, Annenkova, Eleonora, Marakhonov, Andrey, Gusarova, Elena, Demina, Nina, Guseva, Daria, Anisimova, Inga, Degtyareva, Anna, Taran, Natalia, Strokova, Tatiana, Zakharova, Ekaterina
Publicado 2023

A Clinical Case of a Homozygous Deletion in the APOA5 Gene with Severe Hypertriglyceridemia

por Vasiluev, Petr Andreevich, Ivanova, Olga N., Semenova, Natalia A., Strokova, Tatiana V., Taran, Natalia N., Chubykina, Uliana V., Ezhov, Marat V., Zakharova, Ekaterina Y., Dadli, Elena L., Kutsev, Sergey I.
Publicado 2022