Publications by authors named "Corinna Hartmann"

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Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic Review.
Meike Kasten, Corinna Hartmann, Jennie Hampf, Susen Schaake, Ana Westenberger

Mov Disord· May 2018

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Facial twitches in ADCY5-associated disease - Myokymia or myoclonus? An electromyography study.
Sinem Tunc, Norbert Brüggemann, Magdalena K Baaske, Corinna Hartmann, Karen Grütz

Parkinsonism Relat Disord· July 2017

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Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability.
Sofia Steinrücke, Katja Lohmann, Aloysius Domingo, Arndt Rolfs, Tobias Bäumer, Corinna Hartmann

Neurol Genet· October 2016

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Pitfalls in genetic testing: the story of missed SCN1A mutations.
Tania Djémié, Sarah Weckhuysen, Sarah von Spiczak, Gemma L Carvill, Johanna Jaehn, Corinna Hartmann

Mol Genet Genomic Med· July 2016

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Launching the movement disorders society genetic mutation database (MDSGene).
Christina M Lill, Andriy Mashychev, Corinna Hartmann, Katja Lohmann, Connie Marras

Mov Disord· May 2016

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Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis.
Corinna Hartmann, Sarah von Spiczak, Arvid Suls, Sarah Weckhuysen, Gunnar Buyse

Epilepsia· March 2015

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GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.
Gemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, Corinna Hartmann, Rikke S Møller

Neurology· April 2014

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Clarifying the role of the 22q11.2 microdeletion in juvenile myoclonic epilepsy.
Ingo Helbig, Corinna Hartmann, Heather C Mefford

Epilepsy Behav· December 2013

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The unexpected role of copy number variations in juvenile myoclonic epilepsy.
Ingo Helbig, Corinna Hartmann, Heather C Mefford

Epilepsy Behav· July 2013

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