Polina G Tsygankova (P G Tsygankova, Polina Tsygankova)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 24

Top Topics

Duchenne Muscular Dystrophy

Spectrum Disorder

Genome Wide Identification

Top Venues

Vestnik oftalmologii

International journal of molecular sciences

Journal of inherited metabolic disease

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

Publications

Denis Kistol, Polina G Tsygankova, Fatima M Bostanova, Maria Orlova, Ekaterina Zakharova
New Case of Spinocerebellar Ataxia, Autosomal Recessive 4, Due to VPS13D Variants. International journal of molecular sciences 25 (10) (2024)
Yu K Murakhovskaya, N A Andreeva, Polina G Tsygankova, Tatiana Krylova, N L Sheremet
[Long-term changes in morphological and functional parameters of the optic nerve in patients with various genetic variants of hereditary optic neuropathies]. Vestnik oftalmologii 139 (6) (2024)
Fatima M Bostanova, Polina G Tsygankova, Elena A Larshina, Ilya O Nagornov, Yulia V Evseeva, Irina L Krutikhina, Marina E Dzhentemirova, Marina N Kashlakova, Marina S Petukhova, Inna V Sharkova, Ekaterina Y Zakharova
Identification of a Novel Indel Variant in the DARS2 Gene in Russian Patients with Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation. Genes 15 (5) (2024)
Denis Kistol, Polina G Tsygankova, Fatima M Bostanova, Maria Orlova, Ekaterina Zakharova
New Case of Spinocerebellar Ataxia, Autosomal Recessive 4, Due to VPS13D Variants. International journal of molecular sciences 25 (10) (2024)
Fatima M Bostanova, Polina G Tsygankova, Elena A Larshina, Ilya O Nagornov, Yulia V Evseeva, Irina L Krutikhina, Marina E Dzhentemirova, Marina N Kashlakova, Marina S Petukhova, Inna V Sharkova, Ekaterina Y Zakharova
Identification of a Novel Indel Variant in the DARS2 Gene in Russian Patients with Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation. Genes 15 (5) (2024)
N A Andreeva, Yu K Murakhovskaya, Tatiana Krylova, Polina G Tsygankova, N L Sheremet
[Rare pathogenic nucleotide variants of mitochondrial DNA associated with Leber's hereditary optic neuropathy]. Vestnik oftalmologii 139 (6) (2024)
Denis Kistol, Polina G Tsygankova, Fatima M Bostanova, Maria Orlova, Ekaterina Zakharova
New Case of Spinocerebellar Ataxia, Autosomal Recessive 4, Due to VPS13D Variants. International journal of molecular sciences 25 (10) (2024)
Fatima M Bostanova, Polina G Tsygankova, Elena A Larshina, Ilya O Nagornov, Yulia V Evseeva, Irina L Krutikhina, Marina E Dzhentemirova, Marina N Kashlakova, Marina S Petukhova, Inna V Sharkova, Ekaterina Y Zakharova
Identification of a Novel Indel Variant in the DARS2 Gene in Russian Patients with Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation. Genes 15 (5) (2024)
Fatima M Bostanova, Polina G Tsygankova, Elena A Larshina, Ilya O Nagornov, Yulia V Evseeva, Irina L Krutikhina, Marina E Dzhentemirova, Marina N Kashlakova, Marina S Petukhova, Inna V Sharkova, Ekaterina Y Zakharova
Identification of a Novel Indel Variant in the DARS2 Gene in Russian Patients with Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation. Genes 15 (5) (2024)
N L Sheremet, D D Eliseeva, V V Bryukhov, A K Kalashnikova, A A Kaloshina, Yu K Murakhovskaya, Tatiana Krylova, Polina G Tsygankova, Maria Zakharova
[Optic neuropathies as an interdisciplinary subject of research]. Vestnik oftalmologii 139 (3. Vyp. 2) (2023)
D D Eliseeva, A K Kalashnikova, V V Bryukhov, N A Andreeva, N V Zhorzholadze, Yu K Murakhovskaya, Tatiana Krylova, Polina G Tsygankova, Maria Zakharova, N L Sheremet
[Hereditary optic neuropathy associated with demyelinating diseases of the central nervous system]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 123 (7. Vyp. 2) (2023)
Denis Kistol, Polina G Tsygankova, Tatiana Krylova, Igor O Bychkov, Yulia Itkis, Ekaterina Nikolaeva, Svetlana Mikhailova, Maria Sumina, Natalia Pechatnikova, Sergey Kurbatov, Fatima M Bostanova, Ochir Migiaev, Ekaterina Zakharova
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia. International journal of molecular sciences 24 (2) (2023)
Fatima M Bostanova, Polina G Tsygankova, Ilya Nagornov, Elena Dadali, Lyudmila Bessonova, Aleksey Kulesh, Viktor Drobakha, Irina Danchenko, Ilya Kanivets, Ekaterina Zakharova
Four Novel Disease-Causing Variants in the NOTCH3 Gene in Russian Patients with CADASIL. Genes 14 (9) (2023)
Denis Kistol, Polina G Tsygankova, Tatiana Krylova, Igor O Bychkov, Yulia Itkis, Ekaterina Nikolaeva, Svetlana Mikhailova, Maria Sumina, Natalia Pechatnikova, Sergey Kurbatov, Fatima M Bostanova, Ochir Migiaev, Ekaterina Zakharova
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia. International journal of molecular sciences 24 (2) (2023)
Denis Kistol, Polina G Tsygankova, Tatiana Krylova, Igor O Bychkov, Yulia Itkis, Ekaterina Nikolaeva, Svetlana Mikhailova, Maria Sumina, Natalia Pechatnikova, Sergey Kurbatov, Fatima M Bostanova, Ochir Migiaev, Ekaterina Zakharova
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia. International journal of molecular sciences 24 (2) (2023)
Denis Kistol, Polina G Tsygankova, Tatiana Krylova, Igor O Bychkov, Yulia Itkis, Ekaterina Nikolaeva, Svetlana Mikhailova, Maria Sumina, Natalia Pechatnikova, Sergey Kurbatov, Fatima M Bostanova, Ochir Migiaev, Ekaterina Zakharova
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia. International journal of molecular sciences 24 (2) (2023)
Galina V Baydakova, Polina G Tsygankova, Natalia L Pechatnikova, Olga A Bazhanova, Yana D Nazarenko, Ekaterina Y Zakharova
New Acylcarnitine Ratio as a Reliable Indicator of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. International journal of neonatal screening 9 (3) (2023)
Yu K Murakhovskaya, N L Sheremet, M S Shmelkova, Tatiana Krylova, Polina G Tsygankova
[Autosomal recessive optic neuropathies: genetic variants, clinical manifestations]. Vestnik oftalmologii 138 (6) (2022)
N L Sheremet, N A Andreeva, N V Zhorzholadze, Yu K Murakhovskaya, M S Shmelkova, Tatiana Krylova, Polina G Tsygankova
[Metabolic disorders in hereditary optic neuropathies]. Vestnik oftalmologii 138 (4) (2022)
Igor Maev, E V Kolmakova, Sergey N Bardakov, Roman V Deev, Yu A Krivolapov, I E Kotkas, E A Manushina, Sergey Kurbatov, Polina G Tsygankova, A M Emelin, Natalia Bakulina
[Masks hiding mitochondrial neurogastrointestinal encephalomyopathy. Case report]. Terapevticheskii arkhiv 94 (8) (2022)
N L Sheremet, I A Ronzina, N A Andreeva, N V Zhorzholadze, Yu K Murakhovskaya, T A Nevinitsyna, M S Shmelkova, Tatiana Krylova, Polina G Tsygankova, E S Gerasimidi, Konstantin G Lyamzaev, M V Skulachev, E M Karger
[Electrophysiological and psychophysical studies in assessment of visual functions in patients with hereditary optic neuropathy]. Vestnik oftalmologii 138 (2) (2022)
N A Andreeva, Yu K Murakhovskaya, Polina G Tsygankova, Tatiana Krylova, N L Sheremet
[Leber's hereditary optic neuropathy clinical features in patients with mitochondrial DNA m.13513G>A candidate mutation]. Vestnik oftalmologii 138 (5. Vyp. 2) (2022)
N L Sheremet, Tatiana Krylova, Polina G Tsygankova
[New possibilities in diagnosis of hereditary optic neuropathies]. Vestnik oftalmologii 137 (5. Vyp. 2) (2021)
Polina G Tsygankova, Yulia S Itkis, Tatiana D Krylova, Marina V Kurkina, Igor O Bychkov, Aleksandra A Ilyushkina, Viktoria V Zabnenkova, Svetlana V Mikhaylova, Natalia L Pechatnikova, Natalia L Sheremet, Ekaterina Y Zakharova
Plasma FGF-21 and GDF-15 are elevated in different inherited metabolic diseases and are not diagnostic for mitochondrial disorders. Journal of inherited metabolic disease 42 (5) (2019)