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1. neurologie.insel.ch › fileadmin › NeurologieResearch @ Department of Neurology - Insel

   neurologie.insel.ch › fileadmin › Neurologie

   Dr. med. Elena Wenz is a resident at the Department for Neurology, Inselspital, Bern, part of the sleep research group at the Sleep-Wake-Epilepsy-Center, and PhD student at the Graduate School for Health Sciences at the University of Bern, Switzerland. Contact: elena.wenz@insel.ch.

2. academic.oup.com › sleep › advance-articleThe Swiss Primary Hypersomnolence and Narcolepsy Cohort Study ...

   academic.oup.com › sleep › advance-article

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   29. März 2024 · The Swiss Primary Hypersomnolence and Narcolepsy Cohort Study (SPHYNCS) is a multicenter research initiative to identify new biomarkers in central disorders of hypersomnolence (CDH). Whereas narcolepsy type 1 (NT1) is well characterized, other CDH disorders lack precise biomarkers.

3. www.snane.ch › board-2Board of SNaNe – Swiss Narcolepsy Network

   www.snane.ch › board-2

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   His research interests include sleep, stroke, and movement disorders with a translational (human and animal) approach. He served as president of the European Neurological Society (ENS, 2013-4), European Sleep Research Society (ESRS, 2008-12) and Swiss Neurological Society (SNG, 2008-12).

4. www.ncbi.nlm.nih.gov › pmc › articlesJournal of Sleep Research - National Center for Biotechnology...

   www.ncbi.nlm.nih.gov › pmc › articles

   4. Apr. 2021 · Seven Swiss sleep centres, belonging to the Swiss Narcolepsy Network (SNaNe), joined the study and will prospectively enrol over 500 patients with recent onset of excessive daytime sleepiness (EDS), hypersomnia or a suspected central disorder of hypersomnolence (CDH) during a 3‐year recruitment phase.

5. pubmed.ncbi.nlm.nih.gov › 37925849Narcolepsy type 1 and Sydenham chorea - PubMed

   pubmed.ncbi.nlm.nih.gov › 37925849

   30. Okt. 2023 · Patients/methods: We reviewed the literature and report three patients from three European sleep centers who were diagnosed with both SC and NT1 within a few months. Results: We describe the cases of one male (age 10) and two female (age 22 and 10) patients.

6. pubmed.ncbi.nlm.nih.gov › 35299092LMOD3 gene variant in familial periodic hypersomnolence

   pubmed.ncbi.nlm.nih.gov › 35299092

   We report the association of periodic hypersomnia with a polymorphism of the LMOD3-gene in a patient with atypical KLS and a positive family history. Further research is needed to assess the pathological and predictive value of LMOD3 variants in KLS.

7. www.snane.ch › wp-content › uploadsSwiss Narcolepsy bulletin n. 3 | August 2022

   www.snane.ch › wp-content › uploads

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   3. Aug. 2022 · Elena Wenz is a resident at the Department for Neurology at the University Hospital in Bern and a MD-PhD student at the Graduate School for Health Sciences at the University of Bern. She joined the Bernese sleep research group in 2019 and has been significantly involved in the setup of the “ Swiss Primary Hypersomnolence and ...