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Retrospective analysis of 17 patients with mitochondrial membrane protein-associated neurodegeneration diagnosed in Russia.
Parkinsonism Relat Disord. 2021 Mar;84:98-104. doi: 10.1016/j.parkreldis.2021.02.002. Epub 2021 Feb 9.
Parkinsonism Relat Disord. 2021.
PMID: 33607528
Complex Transposon Insertion as a Novel Cause of Pompe Disease.
Bychkov I, Baydakova G, Filatova A, Migiaev O, Marakhonov A, Pechatnikova N, Pomerantseva E, Konovalov F, Ampleeva M, Kaimonov V, Skoblov M, Zakharova E.
Bychkov I, et al. Among authors: kaimonov v.
Int J Mol Sci. 2021 Oct 8;22(19):10887. doi: 10.3390/ijms221910887.
Int J Mol Sci. 2021.
PMID: 34639227
Free PMC article.
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Genetic screening of an endemic mutation in the DYSF gene in an isolated, mountainous population in the Republic of Dagestan.
Bardakov SN, Deev RV, Isaev АА, Khromov-Borisov NN, Kopylov ED, Savchuk МR, Pushkin MS, Presnyakov EV, Magomedova RM, Achmedova PG, Umakhanova ZR, Kaimonov VS, Musatova EV, Blagodatskikh KА, Tveleneva AА, Sofronova YV, Yakovlev IA.
Bardakov SN, et al. Among authors: kaimonov vs.
Mol Genet Genomic Med. 2023 Oct;11(10):e2236. doi: 10.1002/mgg3.2236. Epub 2023 Aug 8.
Mol Genet Genomic Med. 2023.
PMID: 37553796
Free PMC article.
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Complex Multisystem Phenotype With Immunodeficiency Associated With NBAS Mutations: Reports of Three Patients and Review of the Literature.
Khoreva A, Pomerantseva E, Belova N, Povolotskaya I, Konovalov F, Kaimonov V, Gavrina A, Zimin S, Pershin D, Davydova N, Burlakov V, Viktorova E, Roppelt A, Kalinina E, Novichkova G, Shcherbina A.
Khoreva A, et al. Among authors: kaimonov v.
Front Pediatr. 2020 Sep 15;8:577. doi: 10.3389/fped.2020.00577. eCollection 2020.
Front Pediatr. 2020.
PMID: 33042920
Free PMC article.
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Low mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy - a pilot study.
Zaklyazminskaya E, Mikhailov V, Bukaeva A, Kotlukova N, Povolotskaya I, Kaimonov V, Dombrovskaya A, Dzemeshkevich S.
Zaklyazminskaya E, et al. Among authors: kaimonov v.
Sci Rep. 2019 Nov 11;9(1):16409. doi: 10.1038/s41598-019-52911-1.
Sci Rep. 2019.
PMID: 31712709
Free PMC article.
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Frequency distribution of polymorphisms of CYP2C19, CYP2C9, VKORC1 and SLCO1B1 genes in the Yakut population.
Vasilyev FF, Danilova DA, Kaimonov VS, Chertovskih YV, Maksimova NR.
Vasilyev FF, et al. Among authors: kaimonov vs.
Res Pharm Sci. 2016 May-Jun;11(3):259-64.
Res Pharm Sci. 2016.
PMID: 27499796
Free PMC article.
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A novel homozygous mutation causing hereditary tyrosinemia type I in yakut patient in russia: case report.
Maksimova NR, Gurinova EE, Sukhomyasova AL, Danilova AL, Kaimonov VS, Savvina MT, Yakovleva AE, Alekseeva EI.
Maksimova NR, et al. Among authors: kaimonov vs.
Wiad Lek. 2016;69(2 Pt 2):295-8.
Wiad Lek. 2016.
PMID: 27487552
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