Literature DB >> 30713902

Gerstmann-Sträussler-Scheinker Disease Presenting with Atypical Parkinsonism, but Typical Magnetic Resonance Imaging Findings of Prion Disease.

Roser Ribosa-Nogué1,2, Javier Pagonabarraga1,2, Beatriz Gomez-Anson3, Esther Granell-Moreno3, Raquel Sánchez-Valle4, Jaime Kulisevsky1,2.   

Abstract

Entities:  

Keywords:  Gerstmann‐Sträussler‐Scheinker; MRI; corticobasal syndrome; frontotemporal dementia; progressive supanuclear palsy

Year:  2015        PMID： 30713902      PMCID： PMC6353433          DOI： 10.1002/mdc3.12228

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN： 2330-1619


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  8 in total

1.  The MRI pattern of frontal and temporal brain atrophy in fronto-temporal dementia.

Authors:  Marina Boccardi; Mikko P Laakso; Lorena Bresciani; Samantha Galluzzi; Cristina Geroldi; Alberto Beltramello; Hilkka Soininen; Giovanni B Frisoni
Journal:  Neurobiol Aging       Date:  2003 Jan-Feb       Impact factor: 4.673

2.  Atypical parkinsonism due to a D202N Gerstmann-Sträussler-Scheinker prion protein mutation: first in vivo diagnosed case.

Authors:  Annika Plate; Jens Benninghoff; Gerald H Jansen; Elisabeth Wlasich; Sabina Eigenbrod; Alexander Drzezga; Nathalie L Jansen; Hans A Kretzschmar; Kai Bötzel; Dan Rujescu; Adrian Danek
Journal:  Mov Disord       Date:  2013-02       Impact factor: 10.338

3.  Genetic prion disease: the EUROCJD experience.

Authors:  Gábor G Kovács; Maria Puopolo; Anna Ladogana; Maurizio Pocchiari; Herbert Budka; Cornelia van Duijn; Steven J Collins; Alison Boyd; Antonio Giulivi; Mike Coulthart; Nicole Delasnerie-Laupretre; Jean Philippe Brandel; Inga Zerr; Hans A Kretzschmar; Jesus de Pedro-Cuesta; Miguel Calero-Lara; Markus Glatzel; Adriano Aguzzi; Matthew Bishop; Richard Knight; Girma Belay; Robert Will; Eva Mitrova
Journal:  Hum Genet       Date:  2005-11-15       Impact factor: 4.132

4.  Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles.

Authors:  M Yamazaki; K Oyanagi; O Mori; S Kitamura; M Ohyama; A Terashi; T Kitamoto; Y Katayama
Journal:  Acta Neuropathol       Date:  1999-11       Impact factor: 17.088

5.  A novel PRNP Y218N mutation in Gerstmann-Sträussler-Scheinker disease with neurofibrillary degeneration.

Authors:  Ainhoa Alzualde; Begoña Indakoetxea; Isidre Ferrer; Fermin Moreno; Myriam Barandiaran; Ana Gorostidi; Ainara Estanga; Irune Ruiz; Miguel Calero; Fred W van Leeuwen; Begoña Atares; Ramón Juste; Ana Belén Rodriguez-Martínez; Adolfo López de Munain
Journal:  J Neuropathol Exp Neurol       Date:  2010-08       Impact factor: 3.685

6.  [A case of Gerstmann-Sträussler-Scheinker disease with severe muscular atrophy and vertical gaze palsy].

Authors:  N Oba; Y Fujimoto; K Hirata; N Ando; K Saida
Journal:  Rinsho Shinkeigaku       Date:  2000-07

7.  Novel prion protein gene mutation presenting with subacute PSP-like syndrome.

Authors:  D B Rowe; V Lewis; M Needham; M Rodriguez; A Boyd; C McLean; H Roberts; C L Masters; S J Collins
Journal:  Neurology       Date:  2007-03-13       Impact factor: 9.910

8.  Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.

Authors:  T E F Webb; M Poulter; J Beck; J Uphill; G Adamson; T Campbell; J Linehan; C Powell; S Brandner; S Pal; D Siddique; J D Wadsworth; S Joiner; K Alner; C Petersen; S Hampson; C Rhymes; C Treacy; E Storey; M D Geschwind; A H Nemeth; S Wroe; J Collinge; S Mead
Journal:  Brain       Date:  2008-08-30       Impact factor: 13.501
  8 in total
  1 in total

Review 1.  Genotype-Phenotype Correlation in Progressive Supranuclear Palsy Syndromes: Clinical and Radiological Similarities and Specificities.

Authors:  Iñigo Ruiz-Barrio; Andrea Horta-Barba; Ignacio Illán-Gala; Jaime Kulisevsky; Javier Pagonabarraga
Journal:  Front Neurol       Date:  2022-04-26       Impact factor: 4.086
  1 in total

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