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

Segmental Copy Number Loss of SFMBT1 Gene in Elderly Individuals with Ventriculomegaly: A Community-Based Study

1 Jan 2011

Abstract excerpt

OBJECTIVE: Idiopathic normal pressure hydrocephalus (iNPH) is clinically important as a treatable gait disturbance or preventable dementia by shunt operation. We have recently reported that approximately 1.5% of the elderly living in a Japanese community showed ventriculomegaly with features of iNPH on MRI (VIM), which may represent a preclinical stage of iNPH. The purpose of the present study was to identify a...

Read the complete abstract on PubMed

Topics

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

Share to Cerebrospinal fluid and hydrocephalus
Share to Fetal and Pediatric Neurological Disorders
Share to Genetic and Kidney Cyst Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 21325761
DOI: 10.2169/internalmedicine.50.4505

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Segmental Copy Number Loss of SFMBT1 Gene in Elderly Individuals with Ventriculomegaly: A Community-Based StudyPMID 21325761Read ↗

A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study.Semantic proximity Read ↗

Copy number loss in SFMBT1 is common among Finnish and Norwegian patients with iNPHSemantic proximity Read ↗

Genomic causes of multiple cerebral cavernous malformations in a Japanese population.Semantic proximity Read ↗

Genotypic and phenotypic characteristics of juvenile/adult onset vanishing white matter: a series of 14 Chinese patients.Semantic proximity Read ↗

Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia.Semantic proximity Read ↗

SLC26A4 gene copy number variations in Chinese patients with non-syndromic enlarged vestibular aqueduct.Semantic proximity Read ↗

Identification of two novel critical mutations in PCNT gene resulting in microcephalic osteodysplastic primordial dwarfism type II associated with multiple intracranial aneurysms.Semantic proximity Read ↗

Total deletion and a missense mutation of <i>ITPR1</i> in Japanese SCA15 familiesSemantic proximity Read ↗

Familial idiopathic normal pressure hydrocephalus.Semantic proximity Read ↗

Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.Semantic proximity Read ↗

Panventriculomegaly with a wide foramen of Magendie and large cisterna magna: clinical, radiological, and genetic analysisSemantic proximity Read ↗

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