Výsledky vyhledávání - "Ea, Kondrat Eva"

[Peculiarities of sporadic motor neuron disease associated with D90A and G12R mutations in Russian population]

Autor: Vi, Skvortsova, Sa, Limborskaia, Petr Slominsky, Gn, Levitskiĭ, Ni, Levitskaia, Mi, Shadrina, Ea, Kondrat Eva, Os, Brusov, Ai, Lysko, Vb, Karakhan, Av, Alekhin, Av, Serdiuk

Publikováno v: Europe PubMed Central

Fifty-one blood samples of Russian patients with sporadic motor neuron disease were examined for mutations in Cu/Zn superoxide dismutase (SOD-1) gene. One female patient with amyotrophic lateral sclerosis (ALS) was heterozygous for G12R mutation. Thi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::13023021c4eba4d7215598aa57cc6beb
https://pubmed.ncbi.nlm.nih.gov/14681966

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[ACE gene polymorphism in patients with ischemic brain disease]

Autor: Vi, Skvortsova, Sa, Limborskaia, Petr Slominsky, Ea, Kol Tsova, Ea, Kondrat Eva

Publikováno v: Europe PubMed Central

The aim of the present study was to define participation of gene angiotensine converting enzyme (ACE) in the development of atherothrombotic ischemic stroke. 153 patients with cerebrovascular disease were enrolled. The first group consisted of 50 pat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f56780146fba9543aceaddca6ac17f29
https://pubmed.ncbi.nlm.nih.gov/12830537

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[Polymorphism of glutathione S-transferase genes M1 and T1 in patients with motor neuron disease from the city of Moscow]

Autor: Mi, Shadrina, Ea, Kondrat Eva, Petr Slominsky, Ni, Levitskaia, Gn, Levitskiĭ, Va, Skvortsova, Sa, Limborskaia

Publikováno v: Europe PubMed Central

Comparison of the frequency distributions of alleles, genotypes, and genotype combinations of genes GSTM1 and GSTT1 did not show statistically significant differences between patients with motor neuron disease (MND) and a random sample from the Mosco

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b0a9db5ae6040b8664c82ef6c57a41f1
http://europepmc.org/abstract/med/12500684

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[Association of homozygosity for short allele (S) of heavy neurofilament subunit gene with motor neuron disease and oxidative stress development]

Autor: Vi, Skvortsova, Sa, Limborskaia, Pa, Slominskiĭ, Os, Brusov, Vb, Karakhan, Mm, Gerasimova, Ni, Levitskaia, Gn, Levitskiĭ, Maria Shadrina, Ea, Kondrat Eva, Av, Alekhin, Av, Serdiuk, Tm, Botvinko

Publikováno v: Europe PubMed Central

We analyzed distribution of heavy neurofilament (NF-H) gene S/L-polymorphic variants in 51 patients with idiopathic motor neuron disease (MND) vs control group and in relation to superoxide dismutases (SODs) activity and thiobarbituric acid reactive

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ba4da97d27f0bf36d77a0036191378c9
http://europepmc.org/abstract/med/12674703

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[Sporadic amyotrophic lateral sclerosis associated with Asp90Ala CuZn-superoxide dismutase mutations in Russia]

Autor: Vi, Skvortsova, Sa, Limborskaia, Petr Slominsky, Ni, Levitskaia, Gn, Levitskiĭ, Mi, Shadrina, Ea, Kondrat Eva

Publikováno v: Europe PubMed Central

16 blood samples from Russian patients (Moscow) with idiopathic motor neuron disease were analysed for mutations in the CuZn-superoxide dismutase gene. Two patients (12.5%) with amyotrophic lateral sclerosis (ALS) were found to have a disease related

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::18f4b85fadefc7f3665379dad5e5a3b3
http://europepmc.org/abstract/med/10666886

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