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

Camptocormia, axial dystonia, and parkinsonism: phenotypic heterogeneity of a parkin mutation.

Neurology - 22 Apr 2003

Inzelberg R, Hattori N, Nisipeanu P, Abo Mouch S, Blumen S C, Carasso R L, Mizuno Y

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 Arabs
Share to Consanguinity
Share to Dystonic Disorders
Share to Genes, Recessive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Parkinson Disease

Share to Sequence Deletion

Share to Tremor

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 12707457
DOI: 10.1212/01.wnl.0000055809.71968.87

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Camptocormia, axial dystonia, and parkinsonism: phenotypic heterogeneity of a parkin mutation.PMID 12707457Read ↗

Expanding phenotype and clinical heterogeneity in patients with identical mutation of the parkin gene.Semantic proximity Read ↗

Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism.Semantic proximity Read ↗

Parkin disease: a phenotypic study of a large case series.Semantic proximity Read ↗

Mice expressing mutant parkin exhibit hallmark features of Parkinson's disease.Semantic proximity Read ↗

Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's diseaseSemantic proximity Read ↗

Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation.Semantic proximity Read ↗

Heterozygous exon 3 deletion in the Parkin gene in a patient with clinical and radiological MSA-C phenotype.Semantic proximity Read ↗

Phenotypic variability of parkin mutations in single kindred.Semantic proximity Read ↗

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonismSemantic proximity Read ↗

Lewy body pathology and typical Parkinson disease in a patient with a heterozygous (R275W) mutation in the Parkin gene (PARK2).Semantic proximity Read ↗

Genetic Variations and Neuropathologic Features of Patients with PRKN Mutations.Semantic proximity Read ↗

"Dancing feet dyskinesias": a clue to parkin gene mutations.Semantic proximity Read ↗

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