Search

Your search keyword '"Wolfram, S"' showing total 1,435 results

Search Constraints

Start Over You searched for: Author "Wolfram, S" Remove constraint Author: "Wolfram, S"
1,435 results on '"Wolfram, S"'

Search Results

101. Loss of UCP2 attenuates mitochondrial dysfunction without altering ROS production and uncoupling activity.

102. Behavioral changes in G72/G30 transgenic mice

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

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

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

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

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

121. 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

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

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

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

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

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

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

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

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

135. Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier

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

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

139. Open Discussion on A Computable Universe

140. Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration.

141. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

142. SONOGRAPHY OF THE MEDIAN NERVE IN CMT1A, CMT2A, CMTX, AND HNPP

146. Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy

147. Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy

149. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients

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

Catalog

Books, media, physical & digital resources