(Q48667318)

14 February 2018

title

Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies. (English)

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14 February 2018

Creutzfeldt-Jakob disease

main subject

Finland

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M Haltia

1

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14 February 2018

J Kovanen

2

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L G Goldfarb

3

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14 February 2018

P Brown

4

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D C Gajdusek

5

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14 February 2018

publication date

1 September 1991

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14 February 2018

European Journal of Epidemiology

published in

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14 February 2018

volume

7

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14 February 2018

issue

5

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14 February 2018

page(s)

494-500

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14 February 2018

https://scigraph.springernature.com/pub.10.1007/bf00143128

exact match

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cites work

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

1 reference

12 December 2020

New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

1 reference

12 December 2020

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Straussler-Scheinker syndrome

1 reference

12 December 2020

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

1 reference

12 December 2020

Familial Creutzfeldt-Jakob disease

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12 December 2020

Creutzfeldt-Jakob disease of long duration: clinicopathological characteristics, transmissibility, and differential diagnosis.

1 reference

12 December 2020

Creutzfeldt-Jakob disease. II. Clinical, pathologic, and genetic study of a family.

1 reference

12 December 2020

Identical mutation in unrelated patients with Creutzfeldt-Jakob disease.

1 reference

12 December 2020

Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia

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12 December 2020

Cerebral MR and CT imaging in Creutzfeldt-Jakob disease

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12 December 2020

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

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12 December 2020

Clinical and molecular genetic study of a large German kindred with Gerstmann-Straussler-Scheinker syndrome

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12 December 2020

Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families

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12 December 2020

Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin

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12 December 2020

Failure of interferon to modify Creutzfeldt-Jakob disease

1 reference

12 December 2020

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

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12 December 2020

Histocompatibility antigens in familial Creutzfeldt-Jakob disease

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12 December 2020

Descriptive epidemiology of Creutzfeldt-Jakob disease in Finland.

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12 December 2020

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome

1 reference

12 December 2020

The familial occurrence of Creutzfeldt-Jakob disease and Alzheimer's disease

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12 December 2020

Identifiers

DOI

10.1007/BF00143128

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14 February 2018

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14 February 2018