Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits. (Q47950242)

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12 November 2019

review article

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title

Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits (English)

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12 November 2019

0 references

4

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Sabina Capellari

5

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10

P Gambetti

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author name string

C Vital

1

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F Gray

2

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A Vital

3

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R B Petersen

6

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X Ferrer

7

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D Jarnier

8

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J Julien

9

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publication date

1 April 1998

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Neuropathology and Applied Neurobiology

12 November 2019

published in

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volume

24

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issue

2

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page(s)

125-130

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Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene

12 November 2019

cites work

1 reference

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A prion disease with a novel 96-base pair insertional mutation in the prion protein gene.

21 January 2018

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Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.

21 January 2018

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Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation

21 January 2018

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Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

21 January 2018

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Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological features.

21 January 2018

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Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

21 January 2018

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An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family

21 January 2018

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The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype

21 January 2018

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Review: Creutzfeldt-Jakob disease

21 January 2018

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Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene.

21 January 2018

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Diffuse deposition of immunohistochemically labeled prion protein in the granular layer of the cerebellum in a patient with Creutzfeldt-Jakob disease.

21 January 2018

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Prion protein immunocytochemistry helps to establish the true incidence of prion diseases

21 January 2018

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Two novel insertions in the prion protein gene in patients with late-onset dementia.

21 January 2018

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Microwave treatment enhances the immunostaining of amyloid deposits in both the transmissible and non-transmissible brain amyloidoses.

21 January 2018

1 reference

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Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene

21 January 2018

1 reference

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Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

21 January 2018

1 reference

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Inherited prion diseases and transmission to rodents

21 January 2018

1 reference

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10.1046/J.1365-2990.1998.00098.X

21 January 2018

Identifiers

DOI

1 reference

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12 November 2019

1 reference