1,012 results on '"Carelli, V."'
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152. Effect of vehicles on yohimbine permeation across excised hairless mouse skin
153. Mechanism of drug release from silicone microspheres containing Polycarbophil
154. Leber's hereditary optic neuropathy
155. Brain and skeletal muscle bioenergetic failure in familial hypobetalipoproteinaemia.
156. Evaluation of a pH-sensitive semi-interpenetrating polymer network for control of GI drug delivery
157. Changes in mitochondrial complex I activity and coenzyme Q binding site in Leber's hereditary optic neuropathy (LHON)
158. In vitro evaluation of a pH-sensitive hydrogel for control of GI drug delivery from silicone-based matrices
159. MtDNA Mutations Associated with Leber′s Hereditary Optic Neuropathy: Studies on Cytoplasmic Hybrid (Cybrid) Cells
160. Abnormal lactate after effort in healthy carriers of Leber's hereditary optic neuropathy.
161. Lack of association between mitochondrial tRNALeu(UUR) point mutation and cluster headache
162. Enhancement Effects in the Percutaneous Absorption of Alprazolam Through Human Skin in vitro
163. Mitochondrial dysfunction in optic neuropathies: animal models and therapeutic options.
164. Testing Models for Genetic Determination in Migraine
165. Vehicle effects on in vitro skin permeation of and stratum corneum affinity for model drugs caffeine and testosterone
166. ChemInform Abstract: Pyrrolo Quinoline Quinone: A Versatile Biological Electron Carrier.
167. Enhancement effects in the permeation of Alprazolam through hairless mouse skin
168. Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.
169. Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy.
170. The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy.
171. 'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation.
172. Electrical impedance changes and water content in O/W emulsions during evaporation.
173. Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases
174. `Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation
175. Catalytic activities of mitochondrial ATP synthase in patients with mitochondrial DNA T8993G mutation in the ATPase 6 gene encoding subunit a.
176. Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and ^3^1P-MRS study
177. Vehicle Effects in Percutaneous Absorption: In VitroStudy of Influence of Solvent Power and Microscopic Viscosity of Vehicle on Benzocaine Release from Suspension Hydrogels
178. Oxidation of nicotinamide coenzyme dimers by one-electron-accepting proteins
179. Childhood Leber's Hereditary Optic Neuropathy (ND1/3460) With Visual Recovery
180. Oxidation of NAD dimers by horseradish peroxidase
181. New systems for the specific delivery and sustained release of dopamine to the brain
182. Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient
183. Brain and skeletal muscle bioenergetic failure in familial hypobetalipoproteinaemia
184. Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy
185. Mitochondrial DNA haplogroup K is associated with lower risk of Parkinson's disease in Italians
186. Colpocephaly in two siblings: further evidence of a genetic transmission.
187. Electrochemical studies of β-lactams. Part 2. Electrosynthesis of β-lactams via bond formation between C-3 and C-4
188. Adriamicyn-catalyzed photooxidation of NAD dimers to NAD+
189. Effect of tissue degeneration on drug transfer across in vitro rat intestine
190. SEVERE CMT TYPE 2 WITH FATAL ENCEPHALOPATHY ASSOCIATED WITH A NOVEL MFN2SPLICING MUTATION
191. POLGmutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness
192. Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy
193. Next Generation Sequencing results in an Italian cohort of hereditary optic neuropathy patients
194. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484
195. A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy
196. Leber's hereditary optic neuropathy prevalent phenotype in a family segregating the G13042A/NDS mtDNA point mutation
197. P-9Construction of a database for a nation-wideItalian collaborative network of mitochondrial diseases
198. Different OPA1 mutations result in a deficit of in vivo mitochondrial ATP production in patients with autosomal dominant optic atrophy (ADO)
199. Multi-system neurological disease is common in patients with OPA1 mutations
200. Retinal nerve fiber layer changes in unaffected maternal relatives of patients with leber's hereditary optic neuropathy
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