Magzhanov R - Search Results

1

A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease.

Khusnutdinova E, Gilyazova I, Ruiz-Pesini E, Derbeneva O, Khusainova R, Khidiyatova I, Magzhanov R, Wallace DC. Khusnutdinova E, et al. Among authors: magzhanov r. Ann N Y Acad Sci. 2008 Dec;1147:1-20. doi: 10.1196/annals.1427.001. Ann N Y Acad Sci. 2008. PMID: 19076426

2

[Clinical and epidemiological characteristics of hereditary motor-sensory neuropathy 1X caused by the mutation c. 259C> G (p. P87A) in the GJB1 gene of patients from the Republic of Bashkortostan].

Saifullina EV, Magzhanov RV, Khidiyatova IM, Khusnutdinova EK. Saifullina EV, et al. Among authors: magzhanov rv. Zh Nevrol Psikhiatr Im S S Korsakova. 2017;117(3):80-84. doi: 10.17116/jnevro20171173180-84. Zh Nevrol Psikhiatr Im S S Korsakova. 2017. PMID: 28399101 Russian.

3

[Analysis of deletion mutations in the PARK2 gene in idiopathic Parkinson's disease].

Slominskiĭ PA, Miloserdova OV, Popova SN, Giliazova IR, Khidiiatova IV, Magzhanov RV, Khusnutdinova EK, Limborskaia SA. Slominskiĭ PA, et al. Among authors: magzhanov rv. Genetika. 2003 Feb;39(2):223-8. Genetika. 2003. PMID: 12669418 Russian.

4

[Analysis of deletions in the dystrophin gene in patients with Duchenne muscular dystrophy in the Bashkir Republic].

Grinchuk OV, Khidiiatova IM, Kiselev AV, Magzhanov RV, Khusnutdinova EK. Grinchuk OV, et al. Among authors: magzhanov rv. Genetika. 1999 Apr;35(4):551-5. Genetika. 1999. PMID: 10420280 Clinical Trial. Russian.

5

[Expansion and mutation rate in CTG repeats in the myotonic dystrophy gene].

Khidiiatova IM, Fatkhlislamova RI, Magzhanov RV, Popova SN, Slominskiĭ PA, Limborskaia SA, Khusnutdinova EK. Khidiiatova IM, et al. Among authors: magzhanov rv. Genetika. 2000 Oct;36(10):1410-3. Genetika. 2000. PMID: 11094756 Russian.

6

[Analysis of expansion of the triplet repeat (CTG)n in myotonic dystrophy patients from Bashkir].

Slominskiĭ PA, Popova SN, Fatkhlislamova RI, Akhmadeeva LR, Magzhanov RV, Khusnutdinova EK, Limborskaia SA. Slominskiĭ PA, et al. Among authors: magzhanov rv. Genetika. 2000 Jun;36(6):844-8. Genetika. 2000. PMID: 10923268 Russian.

7

[MFN2 gene analysis in patients with hereditary motor and sensory neuropathy from Bashkortostan Republic].

Khidiyatova IM, Skachkova IA, Saifullina EV, Magzhanov RV, Schagina OA, Zinchenko RA, Petrin AN, Khusnutdinova EK. Khidiyatova IM, et al. Among authors: magzhanov rv. Genetika. 2013 Jul;49(7):884-90. doi: 10.7868/s0016675813060040. Genetika. 2013. PMID: 24450158 Russian.

8

[Two novel mutations in gene SPG4 in patients with autosomal dominant spastic paraplegia].

Akhmetgaleyeva AF, Khidiyatova IM, Saifullina EV, Idrisova RF, Magzhanov RV, Khusnutdinova EK. Akhmetgaleyeva AF, et al. Among authors: magzhanov rv. Genetika. 2016 Jun;52(6):691-6. Genetika. 2016. PMID: 29368828 Russian.

9

[Anxiety and depressive disorders in Parkinson's disease].

Akhmadeeva GN, Magzhanov RV, Tayupova GN, Bajtimerov AR, Hidijatova IM. Akhmadeeva GN, et al. Among authors: magzhanov rv. Zh Nevrol Psikhiatr Im S S Korsakova. 2017;117(1. Vyp. 2):54-58. doi: 10.17116/jnevro20171171254-58. Zh Nevrol Psikhiatr Im S S Korsakova. 2017. PMID: 28514334 Review. Russian.

10

[CTG-repeat analysis of myotonin protein kinase gene in Bashkortostan patients with myotonic dystrophy].

Khidiiatova IM, Fatkhlislamova RI, magzhanov RV, Popova SN, Slominskiĭ PA, Limborskaia SA, Khusnutdinova EK. Khidiiatova IM, et al. Among authors: magzhanov rv. Zh Nevrol Psikhiatr Im S S Korsakova. 2002;102(3):54-8. Zh Nevrol Psikhiatr Im S S Korsakova. 2002. PMID: 11957350 Russian.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

42 results

Search Page

Filters