2,183 results on '"CHINNERY, PATRICK F."'
Search Results
152. Current Concepts and Controversies in Neurodegeneration with Brain Iron Accumulation
153. Distinct critical cerebellar subregions for components of verbal working memory
154. Heteroplasmic mitochondrial DNA variants in cardiovascular diseases
155. Contributors
156. Lethal Neonatal LTBL Associated with Biallelic EARS2 Variants: Case Report and Review of the Reported Neuroradiological Features
157. Leber Hereditary Optic Neuropathy
158. Autosomal Dominant Optic Atrophy
159. Additional file 1 of Development and evaluation of rapid data-enabled access to routine clinical information to enhance early recruitment to the national clinical platform trial of COVID-19 community treatments
160. Dissociation of duration-based and beat-based auditory timing in cerebellar degeneration
161. First-line genomic diagnosis of mitochondrial disorders
162. Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency
163. A critical analysis of the combined usage of protein localization prediction methods: Increasing the number of independent data sets can reduce the accuracy of predicted mitochondrial localization
164. Mitochondrial optic neuropathies – Disease mechanisms and therapeutic strategies
165. Leber hereditary optic neuropathy – Therapeutic challenges and early promise
166. The implications of mitochondrial DNA copy number regulation during embryogenesis
167. POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts
168. Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study
169. Response to Newman et al.
170. Shortening the diagnostic odyssey-the impact of whole genome sequencing in the NHS
171. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype
172. ANO10 mutations cause ataxia and coenzyme Q10 deficiency
173. MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial Disease
174. Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction
175. Emerging therapies for mitochondrial disorders
176. Reply: Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion
177. Precision mitochondrial medicine.
178. Mitochondrial diseases
179. Deep Resequencing of Mitochondrial DNA
180. Single-Cell Analysis of Mitochondrial DNA
181. Mitochondrial Disorders Due to Mutations in the Nuclear Genome
182. Mitochondrial DNA depletion induces innate immune dysfunction rescued by IFN-γ
183. Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1)
184. Mitochondrial DNA haplogroups and risk of transient ischaemic attack and ischaemic stroke: a genetic association study
185. The Prevalence and Natural History of Dominant Optic Atrophy Due to OPA1 Mutations
186. Previous Estimates of Mitochondrial DNA Mutation Level Variance Did Not Account for Sampling Error: Comparing the mtDNA Genetic Bottleneck in Mice and Humans
187. A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism
188. Whole-genome sequencing of patients with rare diseases in a national health system
189. Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1)
190. Mitochondrial DNA heteroplasmy is modulated during oocyte development propagating mutation transmission
191. Choosing drugs for UK COVID-19 treatment trials
192. Single-molecule mitochondrial DNA sequencing shows no evidence of CpG methylation in human cells and tissues
193. Shortening the diagnostic odyssey—the impact of whole genome sequencing in the NHS
194. Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study
195. Implications of mitochondrial DNA mutations in human induced pluripotent stem cells
196. How COVID-19 has changed medical research funding
197. Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos
198. The p.Ser107Leu in BICD2 is a mutation ‘hot spot’ causing distal spinal muscular atrophy
199. Reply: Evaluation of exome sequencing variation in undiagnosed ataxias
200. Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy
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