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Year Number of Results
2002 1
2005 1
2007 1
2008 2
2010 2
2011 1
2013 3
2014 3
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2017 1
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2019 6
2020 10
2021 17
2022 16
2023 15

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Page 1
BH4-deficient hyperphenylalaninemia in Russia.
Gundorova P, Kuznetcova IA, Baydakova GV, Stepanova AA, Itkis YS, Kakaulina VS, Alferova IP, Lyazina LV, Andreeva LP, Kanivets I, Zakharova EY, Kutsev SI, Polyakov AV. Gundorova P, et al. Among authors: zakharova ey. PLoS One. 2021 Apr 6;16(4):e0249608. doi: 10.1371/journal.pone.0249608. eCollection 2021. PLoS One. 2021. PMID: 33822819 Free PMC article.
Epidemiology and Genetics of Mucopolysaccharidosis Type VI in Russia.
Voskoboeva E, Semyachkina A, Miklyaev O, Gamzatova A, Mikhaylova S, Vashakmadze N, Baydakova G, Omzar O, Pichkur N, Zakharova E, Kutsev S. Voskoboeva E, et al. Among authors: zakharova e. Front Mol Biosci. 2022 Jan 18;8:780184. doi: 10.3389/fmolb.2021.780184. eCollection 2021. Front Mol Biosci. 2022. PMID: 35118118 Free PMC article.
Association of Rare Variants in ARSA with Parkinson's Disease.
Senkevich K, Beletskaia M, Dworkind A, Yu E, Ahmad J, Ruskey JA, Asayesh F, Spiegelman D, Fahn S, Waters C, Monchi O, Dauvilliers Y, Dupré N, Greenbaum L, Hassin-Baer S, Nagornov I, Tyurin A, Miliukhina I, Timofeeva A, Emelyanov A, Trempe JF, Zakharova E, Alcalay RN, Pchelina S, Gan-Or Z. Senkevich K, et al. Among authors: zakharova e. Mov Disord. 2023 Oct;38(10):1806-1812. doi: 10.1002/mds.29521. Epub 2023 Jun 28. Mov Disord. 2023. PMID: 37381728
Alkaptonuria in Russia: mutational spectrum and novel variants.
Bychkov I, Kamenets E, Kurkina M, Rychkov G, Ilyushkina A, Filatova A, Guseva D, Baydakova G, Nekrasov A, Cheblokov A, Skoblov M, Zakharova E. Bychkov I, et al. Among authors: zakharova e. Eur J Med Genet. 2021 Apr;64(4):104165. doi: 10.1016/j.ejmg.2021.104165. Epub 2021 Feb 20. Eur J Med Genet. 2021. PMID: 33621656
Mitochondrial peptide Mtln contributes to oxidative metabolism in mice.
Averina OA, Permyakov OA, Emelianova MA, Grigoryeva OO, Gulyaev MV, Pavlova OS, Mariasina SS, Frolova OY, Kurkina MV, Baydakova GV, Zakharova EY, Marey MV, Tsarev DA, Tashlitsky VN, Popov VS, Lovat ML, Polshakov VI, Vyssokikh MY, Sergiev PV. Averina OA, et al. Among authors: zakharova ey. Biochimie. 2023 Jan;204:136-139. doi: 10.1016/j.biochi.2022.09.009. Epub 2022 Sep 26. Biochimie. 2023. PMID: 36174793
Association of rare variants in ARSA with Parkinson's disease.
Senkevich K, Beletskaia M, Dworkind A, Yu E, Ahmad J, Ruskey JA, Asayesh F, Spiegelman D, Fahn S, Waters C, Monchi O, Dauvilliers Y, Dupré N, Greenbaum L, Hassin-Baer S, Nagornov I, Tyurin A, Miliukhina I, Timofeeva A, Emelyanov A, Zakharova E, Alcalay RN, Pchelina S, Gan-Or Z. Senkevich K, et al. Among authors: zakharova e. medRxiv. 2023 Mar 13:2023.03.08.23286773. doi: 10.1101/2023.03.08.23286773. Preprint. medRxiv. 2023. PMID: 36993451 Free PMC article. Updated.
Altered level of plasma exosomes in patients with Gaucher disease.
Tatiana S, Stanislav N, Darya K, Luiza G, Konstantin S, Sergey L, Elena V, Galina S, Nikolai V, Arthur K, Elena Z, Roman K, Tatiana U, Alexander S, Ekaterina Z, Anton E, Sofya P. Tatiana S, et al. Among authors: ekaterina z. Eur J Med Genet. 2020 Nov;63(11):104038. doi: 10.1016/j.ejmg.2020.104038. Epub 2020 Aug 18. Eur J Med Genet. 2020. PMID: 32822875
74 results