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| Issue | Title | |
| Vol 14, No 6 (2022) | Gerstmann–Sträussler–Scheinker syndrome with early-onset spinocerebellar ataxia phenotype | Abstract similar documents |
| E. P. Nuzhnyi, N. Y. Abramycheva, E. Y. Fedotova, S. N. Illarioshkin | ||
| "... The article presents a description of the family case of rare hereditary prion disease – Gerstmann ..." | ||
| Vol 16, No 4 (2024) | Gerstmann–Sträussler–Scheinker syndrome with phenotypic change in dynamics and misdiagnosis of a motor neurone disease (clinical case) | Abstract similar documents |
| D. V. Shevchuk, D. A. Grishina, E. P. Nuzhny, M. N. Zakharova | ||
| "... in the prion protein gene PRNP was identified. It is discussed whether GSS should be included ..." | ||
| Vol 12, No 2 (2020) | Creutzfeldt–Jakob disease in the Republic of Sakha (Yakutia) | Abstract PDF (Eng) similar documents |
| T. E. Popova, A. A. Tappakhov, T. K. Davydova, T. Ya. Nikolaeva, Yu. I. Khabarova, M. A. Varlamova, L. T. Okoneshinova | ||
| "... of the pathological isoform of prion protein. The classic clinical presentation of CJD is characterized by rapidly ..." | ||
| Vol 15, No 2 (2023) | Rapidly progressive dementia with early onset associated with the I143T mutation in the PSEN1 gene: a clinical case in a family from Russia | Abstract similar documents |
| Yu. A. Shpilyukova, A. O. Protopopova, N. Yu. Abramycheva, E. Yu. Fedotova, S. N. Illarioshkin | ||
| "... the exclusion of a large number of potentially reversible causes. Prion diseases are frequent in this group ..." | ||
| 1 - 4 of 4 Items | ||
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