Browsing Universitätsbibliographie by Author "Wolking, Stefan"

Now showing items 1-18 of 18

Activation of AMP-activated kinase modulates sensitivity of glioma cells against epidermal growth factor receptor inhibition

Wolking, Stefan (2016)
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy

Wolking, Stefan; Lerche, Holger (2021)
Clinical spectrum of STX1B-related epileptic disorders

Wolking, Stefan; Marquetand, Justus Carl; Weber, Yvonne G.; Lerche, Holger; Schubert, Julian (2019)
Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis

Becker, Felicitas; Wolking, Stefan; Lerche, Holger (2017)
Early-onset familial hemiplegic migraine due to a novel SCN1A mutation

Wolking, Stefan; Hedrich, Ulrike B. S.; Freilinger, Tobias Maximilian; Lerche, Holger (2016)
Episodic itch in a case of spinal glioma

Wolking, Stefan; Lerche, Holger; Dihné, Marcel (2013)
Focal epilepsy in Glucose transporter type 1 (Glut1) defects: case reports and a review of literature

Wolking, Stefan; Becker, Felicitas; Lerche, Holger; Weber, Yvonne G. (2014)
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies

Vittore-Welliong, Debora; Grimm, Alexander; Wolking, Stefan; Lerche, Holger; Schöls, Ludger (2017)
Genetik der epileptischen Enzephalopathien

Wolking, Stefan; Weber, Yvonne G. (2015)
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Becker, Felicitas; Hengsbach, Christian; Lerche, Holger; Rau, Sarah; Weber, Yvonne G.; Wolff, Markus; Wolking, Stefan (2018)
Impact of Genetic Polymorphisms of ABCB1 (MDR1, P-Glycoprotein) on Drug Disposition and Potential Clinical Implications: Update of the Literature

Wolking, Stefan; Schäffeler, Elke; Lerche, Holger; Schwab, Matthias; Nies, Anne (2015)
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study

Wolking, Stefan; Nies, Anne; Schäffeler, Elke; Becker, Felicitas; Weber, Yvonne G.; Schwab, Matthias; Lerche, Holger (2020)
Rare coding variants in genes encoding GABA(A) receptors in genetic generalised epilepsies : an exome-based case-control study

Harrer, Merle; Schubert, Julian; Wolking, Stefan; Becker, Felicitas; Knaus, Julia; Weber, Yvonne G.; Maljevic, Snezana; Lerche, Holger; Niturad, Cristina (2018)
Rare gene deletions in genetic generalized and Rolandic epilepsies

Schubert, Julian; Wolking, Stefan; Lerche, Holger (2018)
Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications

Wolking, Stefan; Lerche, Holger (2021)
Testing association of rare genetic variants with resistance to three common antiseizure medications

Wolking, Stefan; Nies, Anne; Schäffeler, Elke; Becker, Felicitas; Weber, Yvonne G.; Schwab, Matthias; Lerche, Holger (2020)
The modified ultrasound pattern sum score mUPSS as additional diagnostic tool for genetically distinct hereditary neuropathies

Grimm, Alexander; Dammeier, Nele Maria; Lipski, Christina; Wolking, Stefan; Vittore-Welliong, Debora (2016)
The role of common genetic variation in presumed monogenic epilepsies

Wolking, Stefan; Lerche, Holger (2022)

Now showing items 1-18 of 18

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