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History of spinocerebellar ataxia type 1 study and some its unsolved problems

About the Authors

F. A. Platonov
НИИ здоровья СВФУ
Russian Federation


D. G. Tikhonov
НИИ здоровья СВФУ им. М.К. Аммосова; ЯНц КМП СО РАМН
Russian Federation


V. P. Nikolayev
НИИ здоровья СВФУ
Russian Federation


References

1. Dvoreski I.H. Ancient Greek-Russian dictionary / I.H. Dvoreski. – M., 1958, Vol 1. - p. 256.

2. Differential diagnosis of Viliuiski encephalo myelitis: study of hereditary cerebellar ataxia in Yakutia / G.L. Zoubri, L.G. Goldfarb, P.A. Petrov [et al.] //Actual problems of virology and preventing viral disease. - Academy of Medical Sciences, 1972. - p.201-210.

3. Zoubri G.L. Hereditary cerebellar ataxia in Yakutia / G.L. Zoubri, L.G. Goldfarb, A.P. Savinov, M.N. Korotov // First All-Union Conference on Medical Genetics: abstracts. -M., USSR Academy of Medical Sciences. - 1975. - P.60-62.

4. Koneva L.A. Spinocerebellar ataxia type I prediction in the modelled Yakut populations / L.A. Koneva, A.V. Konev, A.N. Kucher // Yakut Medical Journal. - 2009, № 2. - p. 42-45.

5. Hereditary ataxias and paraplegias / S.N. Illa- rioshkin, G.E. Rudenskaya, I.A. Ivanova-Smolen skaya [et al.]. - M.: MEDpress_inform, 2006. – 416 p.

6. Osakovski V.L. On the question of the origin of SCA1-mutations in the Yakut population / V.L. Osakovski, L.G. Goldfarb, F.A. Platonov / Bulletin SB RAMS. - 2004. - № 1. - p. 103-104.

7. Petrov P.A. Viliuiski encephalitis / P.A. Petrov. - Novosibirsk: Nauka, 1987. – 134 p.

8. Bury J.S. A contribution to the symptoma tology of Friedreich’s disease / J.S. Bury // Brain. - 1886;9:145–77.

9. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1 / H.T. Orr, M.Y. Chung, S. Banfi [et al.] // Nat Genet. - 1993; 4: 221–6.

10. Gouriev I.P. Genetic Archeological Per spective on the Origin of Yakuts / I.P. Gouriev // Genetika. - 2004, v 40(4). – P. 560-564.

11. Harding A.E. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias: a study of 11 families, including descendants of the o «Drew family of Walworth» / AE. Harding // Brain. – 1982, 105 : 1.

12. Harding A.E. Classification of the hereditary ataxias and paraplegias / A.E. Harding // Lancet. - 1983; 1: 1151–5. 13. Identification and characterization of the gene causing type 1 spino-cerebellar ataxia / S. Banfi, A. Servadio, M-Y. Chung [et al.] // Nature genet. –1994. – #7. – P.513-520.

13. Jackson J. Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing / J. Jackson, R. Currier, P. Terasaki, N. Morton // N. Engl. J. Med. – 1977; 296:1138-4.

14. Marie P. Sur l’hérédo-ataxie cérébelleuse. Clinique des maladies nerveuses / P. Marie // La semaine médicale. - Paris, 1893. - 13: 444-447.

15. Olivo-pontocerebellar ataxia in a large Iakut kinship in eastern Siberia / L.G. Goldfarb, M.P. Chumakov, P.A. Petrov [et al.] // Neurology. – 1989;39:1527-4.

16. Schut J.W. Hereditary Ataxia A Survey of Certain Clinical, Pathologic and Genetic Features with Linkage Data on Five Additional Hereditary Factors / J.W. Schut // The American Journal Human Genetics. – 1951, Vol.3, No.2. – 93–110.

17. Yakura H. Hereditary ataxia and HLA genotypes / H. Yakura, A. Wakisaka, S. Fujimoto, K. Itakura // N. Engl. J. Med. – 1974; 291:154-12.

18. Slatkin M. Estimating allele age / M. Slatkin, B. Rannala // Annu Rev Genomics Hum Genet. - 2000; 1: 225-249


Review

For citations:


Platonov F.A., Tikhonov D.G., Nikolayev V.P. History of spinocerebellar ataxia type 1 study and some its unsolved problems. Yakut Medical Journal. 2014;(2):114-116. (In Russ.)

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ISSN 1813-1905 (Print)
ISSN 2312-1017 (Online)