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

REM sleep behaviour disorder associated with a neurinoma of the left pontocerebellar angle

1 Jun 2002

Abstract excerpt

Background Abnormal pronuclear formation during fertilisation and subsequent early embryonic arrest results in female infertility. In recent years, with the prevalence of assisted reproductive technology, a few genes have been identified that are involved in female infertility caused by abnormalities in oocyte development, fertilisation and embryonic development. However, the genetic factors responsible for...

Read the complete abstract on PubMed

Topics

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

Share to Fetal and Pediatric Neurological Disorders
Share to Moyamoya disease diagnosis and treatment
Share to Spinal Dysraphism and Malformations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 12023439
DOI: 10.1136/jnnp.72.6.821

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 · 12 closest

REM sleep behaviour disorder associated with a neurinoma of the left pontocerebellar anglePMID 12023439Read ↗

Homozygous mutations in REC114 cause female infertility characterised by multiple pronuclei formation and early embryonic arrest.Semantic proximity Read ↗

Compound Heterozygous REC114 Variants in Dizygotic Twins Causes Meiotic Arrest and Non-Obstructive AzoospermiaSemantic proximity Read ↗

A bi‐allelic REC114 loss‐of‐function variant causes meiotic arrest and nonobstructive azoospermiaSemantic proximity Read ↗

Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes.Semantic proximity Read ↗

Genetic and functional analysis reveals novel mutations in meiotic genes underlying non-obstructive azoospermia.Semantic proximity Read ↗

MEI4 variations drive female reproductive disorders via impaired oocyte abundance and developmental potential.Semantic proximity Read ↗

Analysis of the meiotic recombination gene REC8 for sequence variations in a population with severe male factor infertility.Semantic proximity Read ↗

Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrestSemantic proximity Read ↗

De novo apparent loss-of-function mutations in PRR12 in three patients with intellectual disability and iris abnormalities.Semantic proximity Read ↗

Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure.Semantic proximity Read ↗

Severe Phenotype With RECQL4 Syndrome: A Report of Two Cases.Semantic proximity Read ↗

Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiencySemantic proximity Read ↗

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