Tsygankova PG - Search Results

1

[Optic neuropathies as an interdisciplinary subject of research].

Sheremet NL, Eliseeva DD, Bryukhov VV, Kalashnikova AK, Kaloshina AA, Murakhovskaya YK, Krylova TD, Tsygankova PG, Zakharova MN. Sheremet NL, et al. Among authors: tsygankova pg. Vestn Oftalmol. 2023;139(3. Vyp. 2):63-70. doi: 10.17116/oftalma202313903263. Vestn Oftalmol. 2023. PMID: 37144371 Russian.

2

Gene symbol: WFS1. Disease: Wolfram syndrome.

Tsygankova P, Zakharova EY, Stepina DP. Tsygankova P, et al. Hum Genet. 2008 Feb;123(1):113. Hum Genet. 2008. PMID: 18386376 No abstract available.

3

[Syndrome Leigh caused by mutations in the SURF1 gene: clinical and molecular-genetic characteristics].

Tsygankova PG, Mikhaĭlova SV, Zakharova EIu, Pichkur NA, Il'ina ES, Nikolaeva EA, Rudenskaia GE, Dadali EL, Kolpakchi LM, Fedoniuk ID, Matiushchenko GN. Tsygankova PG, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2010;110(1):25-32. Zh Nevrol Psikhiatr Im S S Korsakova. 2010. PMID: 20436434 Russian.

4

Gene symbol: ACADVL. Disease: Very long chain acyl-CoA dehydrogenase deficiency.

Tsygankova P, Zakharova EY, Baydakova GV. Tsygankova P, et al. Hum Genet. 2008 Oct;124(3):299. Hum Genet. 2008. PMID: 18846621 No abstract available.

5

[Molecular genetics and clinical aspects of monogenic diabetes mellitus].

Peterkova VA, Kuraeva TL, Prokof'ev SA, Emel'ianov AO, Zakharova EIu, Tsygankova PG, Grishina DP. Peterkova VA, et al. Among authors: tsygankova pg. Vestn Ross Akad Med Nauk. 2012;(1):81-6. Vestn Ross Akad Med Nauk. 2012. PMID: 22550716 Russian.

6

[Modern opportunities and prospects for studying pathogenesis, diagnosing and treating hereditary optic neuropathies].

Sheremet NL, Khanakova NA, Nevinitsyna TA, Tsygankova PG, Itkis IuS, Krylova TD, Loginova AN, Chukhrova AL, Venkova LS, Svistunova DM, Chernoivanenko IS, Zakharova EIu, Poliakov AV, Minin AA. Sheremet NL, et al. Among authors: tsygankova pg. Vestn Oftalmol. 2014 Nov-Dec;130(6):62-70. Vestn Oftalmol. 2014. PMID: 25715555 Russian.

7

Previously Unclassified Mutation of mtDNA m.3472T>C: Evidence of Pathogenicity in Leber's Hereditary Optic Neuropathy.

Sheremet NL, Nevinitsyna TA, Zhorzholadze NV, Ronzina IA, Itkis YS, Krylova TD, Tsygankova PG, Malakhova VA, Zakharova EY, Tokarchuk AV, Panteleeva AA, Karger EM, Lyamzaev KG, Avetisov SE. Sheremet NL, et al. Among authors: tsygankova pg. Biochemistry (Mosc). 2016 Jul;81(7):748-54. doi: 10.1134/S0006297916070117. Biochemistry (Mosc). 2016. PMID: 27449621 Free article.

8

[High resolution respirometry in diagnostic of mitochondrial disorders caused by mitochondrial complex I deficiency].

Krylova TD, Tsygankova PG, Itkis YS, Sheremet NL, Nevinitsyna TA, Mikhaylova SV, Zakharova EY. Krylova TD, et al. Among authors: tsygankova pg. Biomed Khim. 2017 Jul;63(4):327-333. doi: 10.18097/PBMC20176304327. Biomed Khim. 2017. PMID: 28862604 Russian.

9

Plasma FGF-21 and GDF-15 are elevated in different inherited metabolic diseases and are not diagnostic for mitochondrial disorders.

Tsygankova PG, Itkis YS, Krylova TD, Kurkina MV, Bychkov IO, Ilyushkina AA, Zabnenkova VV, Mikhaylova SV, Pechatnikova NL, Sheremet NL, Zakharova EY. Tsygankova PG, et al. J Inherit Metab Dis. 2019 Sep;42(5):918-933. doi: 10.1002/jimd.12142. Epub 2019 Jul 24. J Inherit Metab Dis. 2019. PMID: 31260105

10

Three rare pathogenic mtDNA substitutions in LHON patients with low heteroplasmy.

Krylova TD, Sheremet NL, Tabakov VY, Lyamzaev KG, Itkis YS, Tsygankova PG, Andreeva NA, Shmelkova MS, Nevinitsyna TA, Kadyshev VV, Zakharova EY. Krylova TD, et al. Among authors: tsygankova pg. Mitochondrion. 2020 Jan;50:139-144. doi: 10.1016/j.mito.2019.10.002. Epub 2019 Oct 26. Mitochondrion. 2020. PMID: 31669237

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