Atypical parkinsonism due to aD202NGerstmann-Sträussler-Scheinker prion protein mutation: First in vivo diagnosed case-Reference-Cited by-同舟云学术

Atypical parkinsonism due to aD202NGerstmann-Sträussler-Scheinker prion protein mutation: First in vivo diagnosed case

Published:2013-02 Issue:2 Volume:28 Page:241-245
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Plate Annika¹,Benninghoff Jens²,Jansen Gerald H.³⁴,Wlasich Elisabeth¹,Eigenbrod Sabina⁵,Drzezga Alexander⁶,Jansen Nathalie L.⁷,Kretzschmar Hans A.⁵,Bötzel Kai¹,Rujescu Dan²,Danek Adrian¹

Affiliation:

1. Department of Neurology; Ludwig-Maximilians-Universität; Munich Germany

2. Department of Psychiatry; Ludwig-Maximilians-Universität; Munich Germany

3. Canadian Creutzfeldt-Jakob Disease (CJD) Surveillance System and Prion Diseases Program; Ottawa Canada

4. Department of Pathology and Lab Medicine; University of Ottawa; Ottawa Canada

5. National Reference Centre for the Surveillance of Transmissible Spongiform Encephalopathies; Ludwig-Maximilians-Universität; Munich Germany

6. Department of Nuclear Medicine; Technische Universität; Munich Germany

7. Department of Nuclear Medicine; Ludwig-Maximilians-Universität; Munich Germany

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.25188/fullpdf

Reference20 articles.

1. Über ein noch nicht beschriebenes Reflexphänomen bei einer Erkrankung des zerebellaren Systems;Gerstmann;Wien Med Wochenschr,1928

2. Über eine eigenartige hereditär-familiäre Erkrankung des Zentralnervensystems;Gerstmann;Z Neurol,1935

3. The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype;Hainfellner;Brain Pathol,1995

4. Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker;Kretzschmar;Lancet,1991

5. http://www.hgmd.cf.ac.uk/ac/gene.php?gene=PRNP 2012

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic and pathological features encipher the phenotypic heterogeneity of Gerstmann-Sträussler-Scheinker disease;Neurobiology of Disease;2024-06

2. F198S Gerstmann-Sträussler-Scheinker Syndrome With Parkinsonism, Dyskinesia, and Abnormal (I-123)-FP-CIT Single-Photon Emission Computed Tomography: A Case Report;Cureus;2023-12-15

3. Gerstmann—Sträussler disease: a familial case with common PRNP mutation and atypical features;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2023

4. Gerstmann–Sträussler–Scheinker syndrome with early-onset spinocerebellar ataxia phenotype;Neurology, Neuropsychiatry, Psychosomatics;2022-12-19

5. An unusual familial dementia associated with G131V PRNP mutation;European Journal of Neurology;2020-10-18