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

N3 sleep with rapid eye movements in a PCDH19 mutation: a new dissociate state between N3 and REM sleep.

Sleep medicine - 1 Oct 2020

Rupin-Mas Maïlys, Gourfinkel-An Isabelle, Arnulf Isabelle

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 Cadherins
Share to Electroencephalography
Share to Mutation
Share to Protocadherins

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Sleep, REM

Share to Sleep Stages

Source

Identifiers

PMID: 32949989
DOI: 10.1016/j.sleep.2020.07.047

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

N3 sleep with rapid eye movements in a PCDH19 mutation: a new dissociate state between N3 and REM sleep.PMID 32949989Read ↗

PCDH19-Related Epilepsy Syndrome: A Comprehensive Clinical ReviewSemantic proximity Read ↗

PCDH19-clustering epilepsy, pathophysiology and clinical significanceSemantic proximity Read ↗

Epilepsy and NREM-parasomnia caused by novel hemizygous ARHGEF9 mutation.Semantic proximity Read ↗

Epilepsy with PCDH19 mutation masquerading as benign partial epilepsy in infancy.Semantic proximity Read ↗

A de novo gain-of-function KCND3 mutation in early repolarization syndromeSemantic proximity Read ↗

Characteristic phasic evolution of convulsive seizure in PCDH19-related epilepsy.Semantic proximity Read ↗

[Epilepsy with PCDH19 mutation: polypharmacy as a consequence of the complexity and diversity of pathogenesis mechanisms].Semantic proximity Read ↗

[Clinical and genetic characteristics of epilepsy caused by mutations in the PCDH19 gene (OMIM: 300088)].Semantic proximity Read ↗

Characterization of sleep in a mouse model of CLN3 disease revealed sex-specific sleep disturbancesSemantic proximity Read ↗

Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE.Semantic proximity Read ↗

The L450F [Corrected] mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together.Semantic proximity Read ↗

Association of structural polymorphisms in the human period3 gene with delayed sleep phase syndrome.Semantic proximity Read ↗

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