Literature DB >> 10522892

Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob disease.

H Rosenmann1, E Kahana, A D Korczyn, I Kahana, J Chapman, R Gabizon.   

Abstract

Creutzfeldt-Jakob disease (CJD) linked to the E200K mutation of the prion protein (PrP) gene presents within a wide range of phenotypic heterogeneity, including the age at disease onset. We report an earlier disease onset for mutation carriers of the offspring generation when compared with that of their parents, suggesting the possibility of anticipation. A still unidentified environmental or genetic element may affect the age at onset in mutation carriers of different generations.

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Year:  1999        PMID: 10522892     DOI: 10.1212/wnl.53.6.1328

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  8 in total

Review 1.  Genetic PrP Prion Diseases.

Authors:  Mee-Ohk Kim; Leonel T Takada; Katherine Wong; Sven A Forner; Michael D Geschwind
Journal:  Cold Spring Harb Perspect Biol       Date:  2018-05-01       Impact factor: 10.005

Review 2.  Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.

Authors:  Leonel T Takada; Mee-Ohk Kim; Ross W Cleveland; Katherine Wong; Sven A Forner; Ignacio Illán Gala; Jamie C Fong; Michael D Geschwind
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2017-01       Impact factor: 3.568

3.  Increased severity over generations of Charcot-Marie-Tooth disease type 1A.

Authors:  I Steiner; M Gotkine; B Steiner-Birmanns; I Biran; S Silverstein; D Abeliovich; Z Argov; I Wirguin
Journal:  J Neurol       Date:  2008-04-30       Impact factor: 4.849

4.  Genotype-phenotype analysis in inherited prion disease with eight octapeptide repeat insertional mutation.

Authors:  Martin Paucar; Fengqing Xiang; Richard Moore; Ruth Walker; Elisabeth Winnberg; Per Svenningsson
Journal:  Prion       Date:  2013-11-25       Impact factor: 3.931

5.  Ascertainment bias causes false signal of anticipation in genetic prion disease.

Authors:  Eric Vallabh Minikel; Inga Zerr; Steven J Collins; Claudia Ponto; Alison Boyd; Genevieve Klug; André Karch; Joanna Kenny; John Collinge; Leonel T Takada; Sven Forner; Jamie C Fong; Simon Mead; Michael D Geschwind
Journal:  Am J Hum Genet       Date:  2014-10-02       Impact factor: 11.025

6.  Familial multiple sclerosis and association with other autoimmune diseases.

Authors:  Vanesa Pytel; Jordi A Matías-Guiu; Laura Torre-Fuentes; Paloma Montero; Álvaro Gómez-Graña; Rocío García-Ramos; Teresa Moreno-Ramos; Celia Oreja-Guevara; Miguel Fernández-Arquero; Ulises Gómez-Pinedo; Jorge Matías-Guiu
Journal:  Brain Behav       Date:  2017-12-19       Impact factor: 2.708

7.  Age at Death of Creutzfeldt-Jakob disease in subsequent family generation carrying the E200K mutation of the prion protein gene.

Authors:  Maurizio Pocchiari; Anna Poleggi; Maria Puopolo; Marco D'Alessandro; Dorina Tiple; Anna Ladogana
Journal:  PLoS One       Date:  2013-04-02       Impact factor: 3.240

8.  Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies.

Authors:  Anna Ladogana; Pascual Sanchez-Juan; Eva Mitrová; Alison Green; Natividad Cuadrado-Corrales; Raquel Sánchez-Valle; Silvia Koscova; Adriano Aguzzi; Theodoros Sklaviadis; Jerzy Kulczycki; Joanna Gawinecka; Albert Saiz; Miguel Calero; Cornelia M van Duijn; Maurizio Pocchiari; Richard Knight; Inga Zerr
Journal:  J Neurol       Date:  2009-05-15       Impact factor: 4.849

  8 in total

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