Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene. - Test2 - elhamkhani - TriplyDB

Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.

Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.

http://www.wikidata.org/entity/Q33629468

about

Biomarkers for sporadic Creutzfeldt-Jakob disease Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders.The influence of PRNP polymorphisms on human prion disease susceptibility: an update.Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.Creutzfeldt-Jakob Disease with a prion protein gene codon 180 mutation presenting asymmetric cortical high-intensity on magnetic resonance imaging.Pathological progression of genetic Creutzfeldt-Jakob disease with a PrP V180I mutation.First case of V180I rare mutation in a Brazilian patient with Creutzfeldt-Jakob disease.

P2860

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P2860

Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.

http://www.wikidata.org/entity/Q33629468

description

2014 nî lūn-bûn

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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2014 թվականի մայիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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Clinical features of genetic C ...... ion in the prion protein gene.

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Clinical features of genetic C ...... ion in the prion protein gene.

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Clinical features of genetic C ...... ion in the prion protein gene.

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Clinical features of genetic C ...... ion in the prion protein gene.

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Clinical features of genetic C ...... tion in the prion protein gene

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Atsushi Kobayashi

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Hidehiro Mizusawa

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Hiroyuki Murai

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Ichiro Nozaki

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Katsuya Satoh

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Makoto Tomita

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Masahito Yamada

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Masaki Hizume

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Maya Higuma

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Ryuichiro Atarashi

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P2860

Prion diseases of humans and animals: their causes and molecular basis

Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images

Familial Creutzfeldt-Jakob disease with V180I mutation.

Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion.

Sporadic and familial CJD: classification and characterisation.

Clinical features of Creutzfeldt-Jakob disease with V180I mutation.

Glycoform-selective prion formation in sporadic and familial forms of prion disease.

Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases.

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome.

Phenotypic variability in human prion diseases.

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Prion protein family

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