Natalia A Semenova (Natalia Semenova)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 13

Top Topics

Intellectual Disability

Transcranial Magnetic Stimulation

Genome Wide Identification

Top Venues

International journal of molecular sciences

Clinics and practice

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Fatima Bostanova, Olga Levchenko, Margarita Sharova, Natalia A Semenova
Clinical Case of Mild Tatton-Brown-Rahman Syndrome Caused by a Nonsense Variant in DNMT3A Gene. Clinics and practice 14 (3) (2024)
Fatima Bostanova, Olga Levchenko, Margarita Sharova, Natalia A Semenova
Clinical Case of Mild Tatton-Brown-Rahman Syndrome Caused by a Nonsense Variant in DNMT3A Gene. Clinics and practice 14 (3) (2024)
Natalia A Semenova, Olga Mironovich, Olga A Shchagina, Elena Kamenec, Andrey A Marakhonov, Anna V Degtyareva, Natalia Taran, Tatiana Strokova
Clinical Presentation of a Patient with a Congenital Disorder of Glycosylation, Type IIs ( ATP6AP1 ), and Liver Transplantation. International journal of molecular sciences 24 (8) (2023)
Natalia A Semenova, Olga Mironovich, Olga A Shchagina, Elena Kamenec, Andrey A Marakhonov, Anna V Degtyareva, Natalia Taran, Tatiana Strokova
Clinical Presentation of a Patient with a Congenital Disorder of Glycosylation, Type IIs ( ATP6AP1 ), and Liver Transplantation. International journal of molecular sciences 24 (8) (2023)
Natalia A Semenova, Elena A Kamenets, Eleonora Annenkova, Andrey A Marakhonov, Elena Gusarova, Nina Demina, Daria Guseva, Inga Anisimova, Anna V Degtyareva, Natalia Taran, Tatiana Strokova, Ekaterina Zakharova
Clinical Characterization of Alagille Syndrome in Patients with Cholestatic Liver Disease. International journal of molecular sciences 24 (14) (2023)
Natalia A Semenova, Olga Mironovich, Olga A Shchagina, Elena Kamenec, Andrey A Marakhonov, Anna V Degtyareva, Natalia Taran, Tatiana Strokova
Clinical Presentation of a Patient with a Congenital Disorder of Glycosylation, Type IIs ( ATP6AP1 ), and Liver Transplantation. International journal of molecular sciences 24 (8) (2023)
Natalia A Semenova, Olga Mironovich, Olga A Shchagina, Elena Kamenec, Andrey A Marakhonov, Anna V Degtyareva, Natalia Taran, Tatiana Strokova
Clinical Presentation of a Patient with a Congenital Disorder of Glycosylation, Type IIs ( ATP6AP1 ), and Liver Transplantation. International journal of molecular sciences 24 (8) (2023)
Natalia A Semenova, Andrey A Marakhonov, Maria Ampleeva, Marina Kurkina, Galina Baydakova, Mikhail Skoblov, Natalia Taran, Olga Babak, Ekaterina Shchukina, Tatyana Strokova
Hyperammonemia in Russia Due to Carbonic Anhydrase VA Deficiency Caused by Homozygous Mutation p.Lys185Lys (c.555G>A) of the CA5A Gene. International journal of molecular sciences 23 (23) (2022)
Natalia A Semenova, Andrey A Marakhonov, Maria Ampleeva, Marina Kurkina, Galina Baydakova, Mikhail Skoblov, Natalia Taran, Olga Babak, Ekaterina Shchukina, Tatyana Strokova
Hyperammonemia in Russia Due to Carbonic Anhydrase VA Deficiency Caused by Homozygous Mutation p.Lys185Lys (c.555G>A) of the CA5A Gene. International journal of molecular sciences 23 (23) (2022)
Natalia A Semenova, Andrey A Marakhonov, Maria Ampleeva, Marina Kurkina, Galina Baydakova, Mikhail Skoblov, Natalia Taran, Olga Babak, Ekaterina Shchukina, Tatyana Strokova
Hyperammonemia in Russia Due to Carbonic Anhydrase VA Deficiency Caused by Homozygous Mutation p.Lys185Lys (c.555G>A) of the CA5A Gene. International journal of molecular sciences 23 (23) (2022)
Natalia A Semenova, Andrey A Marakhonov, Maria Ampleeva, Marina Kurkina, Galina Baydakova, Mikhail Skoblov, Natalia Taran, Olga Babak, Ekaterina Shchukina, Tatyana Strokova
Hyperammonemia in Russia Due to Carbonic Anhydrase VA Deficiency Caused by Homozygous Mutation p.Lys185Lys (c.555G>A) of the CA5A Gene. International journal of molecular sciences 23 (23) (2022)
Natalia A Semenova, Andrey A Marakhonov, Maria Ampleeva, Marina Kurkina, Galina Baydakova, Mikhail Skoblov, Natalia Taran, Olga Babak, Ekaterina Shchukina, Tatyana Strokova
Hyperammonemia in Russia Due to Carbonic Anhydrase VA Deficiency Caused by Homozygous Mutation p.Lys185Lys (c.555G>A) of the CA5A Gene International journal of molecular sciences 23 (23) (2022)
Andrey A Marakhonov, Magdalena Přechová, Fedor A Konovalov, Alexandra Yu Filatova, Maria A Zamkova, Ilya V Kanivets, Vladimir G Solonichenko, Natalia A Semenova, Rena A Zinchenko, Richard Treisman, Mikhail Yurevich Skoblov
Mutation in PHACTR1 associated with multifocal epilepsy with infantile spasms and hypsarrhythmia. Clinical genetics 99 (5) (2021)