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153. Recombination of Human Mitochondrial DNA

160. Disorganization of the Desmin Cytoskeleton and Mitochondrial Dysfunction in Plectin-Related Epidermolysis Bullosa Simplex with Muscular Dystrophy

162. Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2Pathogenic Variants

169. Genotypes and phenotypes of patients with Lafora disease living in Germany

171. Risk of mitochondrial deletions is affected by the global secondary structure of the mitochondrial genome

172. No evidence for a BRD 2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy

173. Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans

175. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

176. Analysis of shared heritability in common disorders of the brain

177. Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

178. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

179. Analysis of shared heritability in common disorders of the brain

183. Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease

184. 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

185. Carbamazepine- and oxcarbazepine-induced hyponatremia in people with epilepsy

190. Testing association of rare genetic variants with resistance to three common antiseizure medications.

193. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

194. Linear mitochondrial DNA is rapidly degraded by components of the replication machinery

198. Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis

199. Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy

200. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

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