Olga Mironovich (O L Mironovich, O L Shatokhina, Olga Shatokhina)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 25

Top Topics

Botulinum Toxin

Spectrum Disorder

Top Venues

International journal of molecular sciences

Clinical genetics

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

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

Publications

Olga Mironovich, Fatima Bostanova, Maria Bulakh, Anastasia Beresneva, Oxana Ryzhkova
The first case of a point pathogenic variant in the RREB1 gene in Noonan-like Rasopathy. Clinical genetics 105 (5) (2024)
Olga Mironovich, Fatima Bostanova, Maria Bulakh, Anastasia Beresneva, Oxana Ryzhkova
The first case of a point pathogenic variant in the RREB1 gene in Noonan-like Rasopathy. Clinical genetics 105 (5) (2024)
Olga Mironovich, Fatima Bostanova, Maria Bulakh, Anastasia Beresneva, Oxana Ryzhkova
The first case of a point pathogenic variant in the RREB1 gene in Noonan-like Rasopathy. Clinical genetics (2024)
G E Rudenskaya, Daria Guseva, Olga Mironovich, V A Kadnikova, Alexandra Yu Filatova, Mikhail Yurevich Skoblov, Oxana P Ryzhkova
[Developmental and epileptic encephalopathy produced by the ATP1A2 mutation]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 124 (6) (2024)
Olga Mironovich, Fatima Bostanova, Maria Bulakh, Anastasia Beresneva, Oxana Ryzhkova
The first case of a point pathogenic variant in the RREB1 gene in Noonan-like Rasopathy. Clinical genetics 105 (5) (2024)
G E Rudenskaya, Daria Guseva, Olga Mironovich, V A Kadnikova, Alexandra Yu Filatova, Mikhail Yurevich Skoblov, Oxana P Ryzhkova
[Developmental and epileptic encephalopathy produced by the ATP1A2 mutation]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 124 (6) (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, 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)
Olga Mironovich, Valeriia A Kovalskaia, Peter A Sparber, Inna Sharkova, Irina Mishina, Vera Kuznetsova, Oxana P Ryzhkova
TRA2B Gene Splice Variant Linked to Seizures and Neurodevelopmental Delay: A Second Case Study. International journal of molecular sciences 24 (21) (2023)
Aysylu F Murtazina, Sergey Nikitin, Galina Rudenskaya, Inna Sharkova, Artem O Borovikov, Peter A Sparber, Olga A Shchagina, Alena Chukhrova, Oxana P Ryzhkova, Olga Mironovich, Anna A Orlova, Vasilisa Udalova, Ilya Kanivets, Sergey Korostelev, Alexander Polyakov, Elena Dadali, Sergey Kutsev
Genetic and Clinical Spectrum of GNE Myopathy in Russia. Genes 13 (11) (2022)
Olga Mironovich, Nailya Galeeva, Anna Stepanova, Tatiana Markova, Maria Lalayants, Natalia Alekseeva, George Tavarkiladze, Tatiana Vladimirovna Markova, Liudmila Bessonova, Marina Petukhova, Daria Guseva, Inga Anisimova, Alexander Polyakov, Oxana P Ryzhkova, Elena Bliznetz
Spectrum of Genes for Non- GJB2 -Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel. International journal of molecular sciences 23 (24) (2022)
Tatiana Markova, Natalia Alekseeva, Maria Lalayants, Oxana P Ryzhkova, Olga Mironovich, Nailya Galeeva, Elena A Bliznetz, Oleg Belov, Svetlana Chibisova, Alexander Polyakov, George Tavarkiladze
Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss. Journal of personalized medicine 12 (11) (2022)
Olga Mironovich, Nailya Galeeva, Anna Stepanova, Tatiana Markova, Maria Lalayants, Natalia Alekseeva, George Tavarkiladze, Tatiana Vladimirovna Markova, Liudmila Bessonova, Marina Petukhova, Daria Guseva, Inga Anisimova, Alexander Polyakov, Oxana P Ryzhkova, Elena Bliznetz
Spectrum of Genes for Non- GJB2 -Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel. International journal of molecular sciences 23 (24) (2022)
Tatiana Markova, Natalia Alekseeva, Maria Lalayants, Oxana P Ryzhkova, Olga Mironovich, Nailya Galeeva, Elena A Bliznetz, Oleg Belov, Svetlana Chibisova, Alexander Polyakov, George Tavarkiladze
Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss. Journal of personalized medicine 12 (11) (2022)
Olga A Shchagina, Valeriy Fedotov, Tatiana Vladimirovna Markova, Olga Mironovich, Oksana Ryzhkova, Tatiana Fedotova, Aleksander Polyakov
Palmoplantar Keratoderma: A Molecular Genetic Analysis of Family Cases. International journal of molecular sciences 23 (17) (2022)
Olga Mironovich, Nailya Galeeva, Anna Stepanova, Tatiana Markova, Maria Lalayants, Natalia Alekseeva, George Tavarkiladze, Tatiana Vladimirovna Markova, Liudmila Bessonova, Marina Petukhova, Daria Guseva, Inga Anisimova, Alexander Polyakov, Oxana P Ryzhkova, Elena Bliznetz
Spectrum of Genes for Non- GJB2 -Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel. International journal of molecular sciences 23 (24) (2022)
Olga Mironovich, Nailya Galeeva, Anna Stepanova, Tatiana Markova, Maria Lalayants, Natalia Alekseeva, George Tavarkiladze, Tatiana Vladimirovna Markova, Liudmila Bessonova, Marina Petukhova, Daria Guseva, Inga Anisimova, Alexander Polyakov, Oxana P Ryzhkova, Elena Bliznetz
Spectrum of Genes for Non- GJB2 -Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel. International journal of molecular sciences 23 (24) (2022)
G E Rudenskaya, Daria Guseva, Olga Mironovich, V A Kadnikova, E L Dadali, I F Komar'kov, Olga G Novoselova, Oxana P Ryzhkova
[AP4-assocated hereditary spastic paraplegias]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 121 (2) (2021)
Olga Mironovich, Natalia Semenova, Nina Demina, Elena Dadali, Alexander Polyakov, Oxana P Ryzhkova
A Two-Year Clinical Description of a Patient with a Rare Type of Low-GGT Cholestasis Caused by a Novel Variant of USP53. Genes 12 (10) (2021)
G E Rudenskaya, V A Kadnikova, L A Bessonova, Peter A Sparber, Sergey Kurbatov, Olga Mironovich, Fedor A Konovalov, Oxana P Ryzhkova
[Autosomal dominant spastic paraplegias]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 121 (5) (2021)
Maria R Lalayants, Olga Mironovich, Elena A Bliznetz, Tatiana G Markova, Alexander V Polyakov, George Tavarkiladze
[OTOF-related auditory neuropathy spectrum disorder]. Vestnik otorinolaringologii 85 (2) (2020)
Tatiana G Markova, N N Alekseeva, Olga Mironovich, Elena A Bliznetz, Maria R Lalayants, Alexander V Polyakov, George Tavarkiladze
[Hearing loss due to mutations or lack of the gene coding protein stereocillin]. Vestnik otorinolaringologii 85 (2) (2020)
Olga Mironovich, Elena Dadali, Sergey Malmberg, Tatyana Markova, Oxana Ryzhkova, Aleksander Poliakov
Identification of a Novel de Novo Variant in the SYT2 Gene Causing a Rare Type of Distal Hereditary Motor Neuropathy. Genes 11 (11) (2020)