Publications by authors named "Hannah Stamberger"

15Publications

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.

Nat Commun 2020 01 30;11(1):595. Epub 2020 Jan 30.

Institute of Medical Biology, A*STAR, Biopolis, Singapore, 138648, Singapore.

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http://dx.doi.org/10.1038/s41467-020-14360-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992768PMC
January 2020

Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.

Am J Hum Genet 2018 05 12;102(5):744-759. Epub 2018 Apr 12.

Service de Génétique Médicale, CHU Nantes, 9 quai Moncousu, 44093 Nantes Cedex 1, France; l'institut du thorax, INSERM, CNRS, UNIV Nantes, 44007 Nantes, France. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2018.02.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5986661PMC
May 2018

STXBP1 as a therapeutic target for epileptic encephalopathy.

Expert Opin Ther Targets 2017 11 5;21(11):1027-1036. Epub 2017 Oct 5.

a Neurogenetics Group, Center for Molecular Neurology , VIB , Antwerp , Belgium.

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http://dx.doi.org/10.1080/14728222.2017.1386175DOI Listing
November 2017

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Brain 2017 May;140(5):1316-1336

The Danish Epilepsy Centre, Dianalund, Denmark.

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http://dx.doi.org/10.1093/brain/awx054DOI Listing
May 2017

Auditory cortex tACS and tRNS for tinnitus: single versus multiple sessions.

Neural Plast 2014 22;2014:436713. Epub 2014 Dec 22.

Department of Translational Neuroscience, Faculty of Medicine, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, Wilrijk, 2610 Antwerpen, Belgium ; Lab for Clinical & Integrative Neuroscience, School of Behavioral & Brain Science, University of Texas at Dallas, W. 1966 Inwood Road, Dallas, TX 75235, USA.

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http://dx.doi.org/10.1155/2014/436713DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283418PMC
May 2015