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

Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian population.

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques - 1 May 2006

Dupré Nicolas, Bouchard Jean-Pierre, Brais Bernard, Rouleau Guy A

Abstract excerpt

Historical events have shaped the various regional gene pools of the French-Canadian (FC) population, leading to increased prevalence of some rare diseases. The first studies of these founder effects were performed in large part by astute clinicians such as André Barbeau. In collaboration with ot...

Read the complete abstract on PubMed

Topics

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

Share to Central Nervous System
Share to Chromosome Mapping
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Paraparesis, Spastic

Share to Peripheral Nerves

Share to Peripheral Nervous System Diseases

Share to Quebec

Share to Spinocerebellar Degenerations

Source

Identifiers

PMID: 16736723
DOI: 10.1017/s031716710000490x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16736723-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian population.PMID 16736723Read ↗

Clinical and genetic study of hereditary spastic paraplegia in CanadaSemantic proximity Read ↗

Autosomal recessive spastic ataxia of Charlevoix-Saguenay: a family report from South Brazil.Semantic proximity Read ↗

A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.Semantic proximity Read ↗

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1.Semantic proximity Read ↗

Diversity of ARSACS mutations in French-Canadians.Semantic proximity Read ↗

Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.Semantic proximity Read ↗

OVERWHELMING GENETIC HETEROGENEITY AND EXHAUSTING MOLECULAR DIAGNOSTIC PROCESS IN CHRONIC AND PROGRESSIVE ATAXIAS: <i>FACING IT UP WITH AN ALGORITHM, A GENE, A PANEL AT A TIME</i>Semantic proximity Read ↗

Review of the Genetic Spectrum of Hereditary Spastic Paraplegias in the Middle East and North Africa RegionsSemantic proximity Read ↗

Hereditary ataxias: overview.Semantic proximity Read ↗

Genetic and Epidemiological Study of Adult Ataxia and Spastic Paraplegia in Eastern Quebec.Semantic proximity Read ↗

The genetic landscape of sporadic adult-onset degenerative ataxia: a multi-modal genetic study of 377 consecutive patients from the longitudinal multi-centre SPORTAX cohortSemantic proximity Read ↗

First case of Autosomal recessive spastic ataxia of Charlevoix-Saguenay in the Middle eastSemantic proximity Read ↗

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