Khusnutdinova EK - Search Results

1

[Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan].

Khidiianova IM, Bagautdinova EG, Galieva DV, Krupina NB, Shchagina OA, Tiburkova TB, Magzhanov RV, Poliakov AV, Khusnutdinova EK. Khidiianova IM, et al. Among authors: khusnutdinova ek. Genetika. 2008 Oct;44(10):1385-91. Genetika. 2008. PMID: 19062535 Russian.

2

[Molecular genetic analysis of phenylketonuria in Bashkiria].

Viktorova TV, Murzabaeva SSh, Karunas AU, Magzhanov RV, Khusnutdinova EK. Viktorova TV, et al. Among authors: khusnutdinova ek. Genetika. 1997 Jul;33(7):992-5. Genetika. 1997. PMID: 9378295 Russian.

3

[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: khusnutdinova ek. Genetika. 1999 Apr;35(4):551-5. Genetika. 1999. PMID: 10420280 Clinical Trial. Russian.

4

[Analysis of mutations and haplotypes of polymorphic markers in patients with Wilson-Konovalov disease from Bashkir].

Karunas AS, Mersiianova IV, Poliakov AV, Evgrafov OV, Khusnutdinova EK. Karunas AS, et al. Among authors: khusnutdinova ek. Genetika. 2000 Jul;36(7):972-9. Genetika. 2000. PMID: 10994503 Russian.

5

[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: khusnutdinova ek. Genetika. 2013 Jul;49(7):884-90. doi: 10.7868/s0016675813060040. Genetika. 2013. PMID: 24450158 Russian.

6

[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: khusnutdinova ek. 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.

7

[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: khusnutdinova ek. Genetika. 2003 Feb;39(2):223-8. Genetika. 2003. PMID: 12669418 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: khusnutdinova ek. Genetika. 2016 Jun;52(6):691-6. Genetika. 2016. PMID: 29368828 Russian.

9

[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: khusnutdinova ek. Genetika. 2000 Jun;36(6):844-8. Genetika. 2000. PMID: 10923268 Russian.

10

[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: khusnutdinova ek. Genetika. 2000 Oct;36(10):1410-3. Genetika. 2000. PMID: 11094756 Russian.

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