Chukhrova AL - Search Results

1

[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: chukhrova al. Vestn Oftalmol. 2014 Nov-Dec;130(6):62-70. Vestn Oftalmol. 2014. PMID: 25715555 Russian.

2

[DNA-diagnosis of Emery-Dreifuss muscular dystrophy].

Tverskaia SM, Rudenskaia GE, Chukhrova AL, Poliakov AV. Tverskaia SM, et al. Among authors: chukhrova al. Zh Nevrol Psikhiatr Im S S Korsakova. 2003;103(6):25-8. Zh Nevrol Psikhiatr Im S S Korsakova. 2003. PMID: 12872622 Russian.

3

[Clinical and molecular genetic analysis of hereditary optic neuropathies].

Avetisov SÉ, Sheremet NL, Vorob'eva OK, Eliseeva ÉG, Chukhrova AL, Loginova AN, Khanakova NA, Poliakov AV. Avetisov SÉ, et al. Among authors: chukhrova al. Vestn Oftalmol. 2013 Mar-Apr;129(2):8-13. Vestn Oftalmol. 2013. PMID: 23808173 Russian.

4

[Hereditary optic neuropathies: clinical and molecular genetic characteristics].

Khanakova NA, Sheremet NL, Loginova AN, Chukhrova AL, Poliakov AV. Khanakova NA, et al. Among authors: chukhrova al. Vestn Oftalmol. 2013 Nov-Dec;129(6):82-7. Vestn Oftalmol. 2013. PMID: 24624809 Review. Russian.

5

[Morphological changes in retina and optic nerve head in patients with Leber's hereditary optic neuropathy].

Avetisov SE, Sheremet NL, Fomin AV, Galoian NS, Khanakova NA, Zhorzholadze NV, Loginova AN, Chukhrova AL, Poliakov AV. Avetisov SE, et al. Among authors: chukhrova al. Vestn Oftalmol. 2014 Jan-Feb;130(1):4-8, 10-1. Vestn Oftalmol. 2014. PMID: 24684059 Russian.

6

[Stargardt's disease and abiotrophy of Franceschetti (fundus flavimaculatus): pathogenetic, clinical, and molecular genetic characteristics].

Bondarenko MT, Zhorzholadze NV, Sheremet NL, Ronzina IA, Galoian NS, Loginova AN, Chukhrova AL, Poliakov AV. Bondarenko MT, et al. Among authors: chukhrova al. Vestn Oftalmol. 2014 Mar-Apr;130(2):72-6. Vestn Oftalmol. 2014. PMID: 24864504 Review. Russian.

7

[Molecular genetic diagnosis of Stargardt disease].

Sheremet NL, Zhorzholadze NV, Ronzina IA, Grushke IG, Kurbatov SA, Chukhrova AL, Loginova AN, Shcherbakova PO, Tanas AS, Polyakov AV, Strel'nikov VV. Sheremet NL, et al. Among authors: chukhrova al. Vestn Oftalmol. 2017;133(4):4-11. doi: 10.17116/oftalma201713344-11. Vestn Oftalmol. 2017. PMID: 28980559 Free article. Russian.

8

[Clinical, genealogical and molecular genetic study of Emery-Dreifuss muscular dystrophy].

Rudenskaia GE, Tverskaia SM, Chukhrova AL, Zakliaz'minskaia EV, Kuropatkina IuV, Dadali EL, Perminov VS, Poliakov AV. Rudenskaia GE, et al. Among authors: chukhrova al. Zh Nevrol Psikhiatr Im S S Korsakova. 2006;106(10):58-65. Zh Nevrol Psikhiatr Im S S Korsakova. 2006. PMID: 17117676 Russian.

9

[Molecular analysis of the Y chromosome in XX sex-reversed patients].

Chernykh VB, Chukhrova AL, Vasserman NN, Il'ina EV, Karmanov ME, Fedotov VP, Poliakov AV. Chernykh VB, et al. Among authors: chukhrova al. Genetika. 2008 Feb;44(2):236-41. Genetika. 2008. PMID: 18619043 Russian.

10

[Screening for deletion in patients with Duchenne's myodystrophy by multiplex amplification].

Chukhrova AL, Malygina NA, Poliakov AV, Zaĭtseva SP, Sitnikov VF, Dadali EL, Kamennykh LN, Khrennikov VIu, Badalian LO, Evgrafov OV. Chukhrova AL, et al. Tsitol Genet. 1994 Jul-Aug;28(4):80-3. Tsitol Genet. 1994. PMID: 7801388 Russian.

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