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Clinical cases of amyotrophic lateral sclerosis concurrent with hydromyelia.
Bogdanov EI, Mendelevich EG, Khabibrakhmanov AN, Bogdanov SE, Mukhamedzhanova GR, Mukhamedyarov MM. Bogdanov EI, et al. Among authors: bogdanov se. Clin Case Rep. 2021 Feb 2;9(3):1571-1576. doi: 10.1002/ccr3.3832. eCollection 2021 Mar. Clin Case Rep. 2021. PMID: 33768891 Free PMC article.
[Family cases of syringomyelia and Arnold-Chiari anomalies].
Mendelevich EG, Bogdanov EI, Chuvashaev IR. Mendelevich EG, et al. Among authors: bogdanov ei. Zh Nevrol Psikhiatr Im S S Korsakova. 2000;100(12):93-5. Zh Nevrol Psikhiatr Im S S Korsakova. 2000. PMID: 11195549 Russian. No abstract available.
[Clinical and neuro-visual study of syringomyelia].
Mendelevich EG, Bogdanov EI, Mikhaĭlov MK. Mendelevich EG, et al. Among authors: bogdanov ei. Zh Nevrol Psikhiatr Im S S Korsakova. 2002;102(7):36-40. Zh Nevrol Psikhiatr Im S S Korsakova. 2002. PMID: 12161865 Russian.
Cerebellar Atrophy and Changes in Cytokines Associated with the CACNA1A R583Q Mutation in a Russian Familial Hemiplegic Migraine Type 1 Family.
Khaiboullina SF, Mendelevich EG, Shigapova LH, Shagimardanova E, Gazizova G, Nikitin A, Martynova E, Davidyuk YN, Bogdanov EI, Gusev O, van den Maagdenberg AMJM, Giniatullin RA, Rizvanov AA. Khaiboullina SF, et al. Among authors: bogdanov ei. Front Cell Neurosci. 2017 Aug 29;11:263. doi: 10.3389/fncel.2017.00263. eCollection 2017. Front Cell Neurosci. 2017. PMID: 28900389 Free PMC article.
Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing.
Musolf AM, Ho WSC, Long KA, Zhuang Z, Argersinger DP, Sun H, Moiz BA, Simpson CL, Mendelevich EG, Bogdanov EI, Bailey-Wilson JE, Heiss JD. Musolf AM, et al. Among authors: bogdanov ei. Eur J Hum Genet. 2019 Oct;27(10):1599-1610. doi: 10.1038/s41431-019-0457-7. Epub 2019 Jun 21. Eur J Hum Genet. 2019. PMID: 31227808 Free PMC article.
70 results