Gerstmann–Sträussler–Scheinker syndrome with early-onset spinocerebellar ataxia phenotype-Reference-Cited by-同舟云学术

Gerstmann–Sträussler–Scheinker syndrome with early-onset spinocerebellar ataxia phenotype

Published:2022-12-19 Issue:6 Volume:14 Page:63-66
ISSN:2310-1342
Container-title:Neurology, Neuropsychiatry, Psychosomatics
language:
Short-container-title:RJTAO

Author:

Nuzhnyi E. P.¹^ORCID,Abramycheva N. Y.¹,Fedotova E. Y.¹^ORCID,Illarioshkin S. N.¹^ORCID

Affiliation:

1. Research Center of Neurology

Publisher

IMA Press, LLC

Subject

Psychiatry and Mental health,Neurology (clinical),Clinical Psychology

Reference19 articles.

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2. Shpilyukova YuA, Seliverstov YuA, Nuzhny EP. A clinical case of fatal familial insomnia with a transient positive response to corticosteroids. Annaly klinicheskoy i experimental'noy nevrologii = Annals of Clinical and Experimental Neurology. 2020;14(4):88-95. doi:10.25692/ACEN.2020.4.12 (In Russ.).

3. Smid J, Studart A Neto, Landemberger MC, et al. High phenotypic variability in Gerstmann–Sträussler–Scheinker disease. Arq Neuropsiquiatr. 2017;75(6):331-8. doi:10.1590/0004-282X20170049

4. Tesar A, Matej R, Kukal J, et al. Clinical variability in P102L Gerstmann–Sträussler–Scheinker syndrome. Ann Neurol. 2019;86(5):643-52. doi:10.1002/ana.25579

5. Gerstmann J, Sträussler E, Scheinker J. Über eine eigenartige hereditär-familiäre Erkrankung des Zentralnervensystems. Z Neurol. 1936;154:736-62.

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