Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation.

Journal of neurology - 1 Dec 2002

Shiraishi Atsushi, Mizusawa Hidehiro, Yamada Masahito

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Leucine
Share to Mutation
Share to Pedigree
Share to Prion Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Prions

Share to Proline

Source

Identifiers

PMID: 12529802
DOI: 10.1007/s00415-002-0907-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation.PMID 12529802Read ↗

Genetic PrP Prion Diseases.Semantic proximity Read ↗

A novel familial prion disease causing pan‐autonomic‐sensory neuropathy and cognitive impairmentSemantic proximity Read ↗

Late onset hereditary sensory and autonomic neuropathy with cognitive impairment associated with Y163X prion mutation.Semantic proximity Read ↗

Prion disease.Semantic proximity Read ↗

Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.Semantic proximity Read ↗

A new variant of prion disease.Semantic proximity Read ↗

Neurocognitive & neuropsychiatric phenotypes of PARK2-associated early-onset Parkinson's disease in two siblings.Semantic proximity Read ↗

Inherited prion diseases and transmission to rodents.Semantic proximity Read ↗

Clinical findings and diagnosis in genetic prion diseases in Germany.Semantic proximity Read ↗

An inherited prion disease with a PrP P105L mutationSemantic proximity Read ↗

WITHDRAWN: Adult-onset Alexander disease in people living with HIV and a novel mutation in GFAPSemantic proximity Read ↗

Perspectives: neurobiology. PrP's double causes trouble.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.