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

Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism

1 Jul 1996

Abstract excerpt

We present the clinical features of 17 patients from 12 Japanese families with familial juvenile parkinsonism suggesting autosomal-recessive inheritance (AR-JP). Because the marriages of the parents in all but one family were consanguineous and all patients were only first generation, an autosomal-recessive trait was strongly suspected. Analysis of the clinical features showed female predominance, mean age at...

Read the complete abstract on PubMed

Topics

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

Share to Lysosomal Storage Disorders Research
Share to Neurological diseases and metabolism
Share to Parkinson's Disease Mechanisms and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 8710071
DOI: 10.1212/wnl.47.1.160

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonismPMID 8710071Read ↗

[The clinical and genetic characteristics of autosomal recessive juvenile Parkinsonism in a Chinese family].Semantic proximity Read ↗

[Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism].Semantic proximity Read ↗

PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonism.Semantic proximity Read ↗

A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation.Semantic proximity Read ↗

Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism.Semantic proximity Read ↗

Juvenile-onset parkinsonism with pyramidal signs due to compound heterozygous mutations in the F-Box only protein 7 gene.Semantic proximity Read ↗

An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene.Semantic proximity Read ↗

Juvenile ParkinsonismSemantic proximity Read ↗

Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.Semantic proximity Read ↗

A novel mutation of PDE8B Gene in a Japanese family with autosomal-dominant striatal degeneration.Semantic proximity Read ↗

Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin gene.Semantic proximity Read ↗

Autosomal dominant diffuse Lewy body disease.Semantic proximity Read ↗

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