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101. PACS Reliability Issues

102. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

103. Distinct gene-set burden patterns underlie common generalized and focal epilepsies

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

105. Distinct segregation of the pathogenic m.5667G>A mitochondrial tRNAAsn mutation in extraocular and skeletal muscle in chronic progressive external ophthalmoplegia

106. Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy

107. Behavioral changes in G72/G30 transgenic mice

109. Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications

110. Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With

111. Heterozygous variants in KCNC2 cause a broad spectrum of epilepsy phenotypes associated with characteristic functional alterations

112. Heterozygous variants in KCNC2 cause a broad spectrum of epilepsy phenotypes associated with characteristic functional alterations 2021.05.21.21257099

115. Image restoration in frequency space using complex-valued CNNs

116. Prevalence of electrocardiographic markers associated with myocardial fibrosis in masters athletes: a cohort study

117. A metabolomics perspective on clorobiocin biosynthesis: discovery of bromobiocin and novel derivatives through LC-MSE-based molecular networking

119. Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy

120. Molecular and Functional Effects of Loss of Cytochrome c Oxidase Subunit 8A

121. Impairment of mitochondrial oxidative phosphorylation in skin fibroblasts of SALS and FALS patients is rescued by in vitro treatment with ROS scavengers

122. Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases

123. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

124. Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy

125. Heterozygous variants in KCNC2 cause a broad spectrum of epilepsy phenotypes associated with characteristic functional alterations 2021.05.21.21257099

126. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

130. Cerebral MRI in a prospective cohort study on depression and atherosclerosis: the BiDirect sample, processing pipelines, and analysis tools

131. Changes in real-world walking speed following 60-day bed-rest

133. 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

136. Heterozygous variants in KCNC2 cause a broad spectrum of epilepsy phenotypes associated with characteristic functional alterations

137. Impairment of mitochondrial oxidative phosphorylation in skin fibroblasts of SALS and FALS patients is rescued by in vitro treatment with ROS scavengers

138. Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

139. A>G substitutions on a heavy chain of mitochondrial genome marks an increased level of aerobic metabolism in warm versus cold vertebrates

140. Pharmacoresponse in genetic generalized epilepsy:a genome-wide association study

141. Epilepsy Subtype-Specific Copy Number Burden Observed in a Genome-Wide Study of 17 458 Subjects

142. Cytosolic, but not matrix, calcium is essential for adjustment of mitochondrial pyruvate supply

143. Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in mice

144. Inheritance of mitochondrial DNA recombinants in double-heteroplasmic families: Potential implications for phylogenetic analysis

145. Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study

146. Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in mice

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

148. Elongation differences between the sub-tendons of gastrocnemius medialis and lateralis during plantarflexion in different frontal plane position of the foot

149. Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study

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