Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.

doi:10.1111/jsr.12044

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

Community

Back to search

Article

Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.

Journal of sleep research - 1 Oct 2013

Luca Gianina, Haba-Rubio José, Dauvilliers Yves, Lammers Gert-Jan, Overeem Sebastiaan, Donjacour Claire E, Mayer Geert, Javidi Sirous, Iranzo Alex, Santamaria Joan, Peraita-Adrados Rosa, Hor Hyun, Kutalik Zoltan, Plazzi Giuseppe, Poli Francesca, Pizza Fabio, Arnulf Isabelle, Lecendreux Michel, Bassetti Claudio, Mathis Johannes, Heinzer Raphael, Jennum Poul, Knudsen Stine, Geisler Peter, Wierzbicka Aleksandra, Feketeova Eva, Pfister Corinne, Khatami Ramin, Baumann Christian, Tafti Mehdi

Abstract excerpt

The aim of this study was to describe the clinical and PSG characteristics of narcolepsy with cataplexy and their genetic predisposition by using the retrospective patient database of the European Narcolepsy Network (EU-NN). We have analysed retrospective data of 1099 patients with narcolepsy diagnosed according to International Classification of Sleep Disorders-2. Demographic and clinical characteristics,...

Read the complete abstract on PubMed

Topics

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

Share to Delayed Diagnosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Europe

Share to Neuropeptides

Share to Orexins

Share to Polysomnography

Share to Principal Component Analysis

Share to Sex Characteristics

Share to Sleep Stages

Source

Open in PubMed

Identifiers

PMID: 23496005
DOI: 10.1111/jsr.12044

Genes

TEAD4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.PMID 23496005Read ↗

Genetics of narcolepsySemantic proximity Read ↗

The European Narcolepsy Network (EU-NN) database.Semantic proximity Read ↗

Narcolepsy without cataplexy: 2 subtypes based on CSF hypocretin-1/orexin-A findings.Semantic proximity Read ↗

[Narcolepsy].Semantic proximity Read ↗

Narcolepsy type 1 features across the life span: age impact on clinical and polysomnographic phenotype.Semantic proximity Read ↗

The epidemiology of narcolepsy.Semantic proximity Read ↗

Validation of the ICSD-2 criteria for CSF hypocretin-1 measurements in the diagnosis of narcolepsy in the Danish population.Semantic proximity Read ↗

Age at onset of narcolepsy in two large populations of patients in France and Quebec.Semantic proximity Read ↗

Early- and late-onset narcolepsy: possibly two distinct clinical phenotypes.Semantic proximity Read ↗

Narcolepsy type 1: an environment-influenced disease.Semantic proximity Read ↗

Course and severity of post-H1N1 narcolepsy type 1: a long-term prospective cohort studySemantic proximity Read ↗

Narcolepsy with cataplexy.Semantic proximity Read ↗

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