1,012 results on '"Carelli V."'
Search Results
102. X-inactivation pattern in multiple tissues from two Leber's hereditary optic neuropathy (LHON) patients
103. EFFETTI IN VITRO DELLA NUOVA FIBRA ANFIBOLICA FLUORO- EDENITE SU MACROFAGI UMANI
104. Radon in indoor air of primary schools: a systematic survey to evaluate factors affecting radon concentration levels and their variability
105. Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy
106. Gene therapy with the ND4 subunit gene recoded in the universal genetic code reverses a mitochondrial deficiency causing Leber Hereditary optic neuropathy. 54Th Annual Meeting of the America Academy of Neurology. Denver (USA) 15-20 aprile 2002
107. ANTIOXIDANT CAPACITY IN CYBRIDS HARBORING THE THREE MTDNA RELATED TO COMPLEX I MUTATIONS SUBUNITS AND PRIMARILY ASSOCIATED WITH LEBER'S (LHON)
108. Cure of a mitochondrial deficiency causing leber hereditary optic neuropathy?
109. Gene therapy with the ND4 subunit gene recoded in the universal genetic code reverses a mitochondrial deficiency causing Leber hereditary optic neuropathy (LHON)
110. Analysis of ROS production and antioxidant machinery in osteosarcoma derived cybrid cell lines carryng caucasic mtDNA haplogroups H,J and T
111. Antioxidant capacity in cybrids harbouring the three mtDNA mutations primarly associated with Leber’s (LHON)
112. derivati della colina per il trattamento della malattia di Alzheimer
113. Melanopsin retinal ganglion cells and circadian dysfunction in Alzheimer´s disease
114. The unsolved genetics of LHON: Beyond mtDNA primary mutations what else?
115. Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α
116. One European-specific mt-DNA background plays a role in the expression of Leber Hereditary Optic Neuropathy
117. Human callus as a material to model stratum corneum
118. Leber herediatry optic neuropathy (LHON): bochemical effect of 11778/ND4 and 3460/ND1 mutations and correlatio with the mitochondrial genotype
119. 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
120. Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy
121. INFLUENCE OF STERIC HINDRANCE ON THE REGIO- AND STEROSELECTIVITY OF PYRIDINYL RADICAL DIMERIZATION
122. INFLUENCE OF STERIC HINDRANCE ON THE 3-CARBAMOIL-PYRIDINYL RADICAL DIMERIZATION
123. Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies
124. Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?
125. Functional alteration of mitochondrial complex I in affected and nonaffected individuals with 11778/ND4 Leber's hereditary optic neuropathy (LHON)
126. Mitochondrial complex I and cell death: a semi-automatic shotgun model
127. Idebenone Treatment In Leber's Hereditary Optic Neuropathy
128. Assessment of long-term radon concentration measurement precision in field conditions (Serbian Schools) for a survey carried out by an international collaboration
129. Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy
130. ARYLSULFATASE A PSEUDODEFICIENCY (ASAPD) IN NEUROLEPTIC MALIGNANT SYNDROME (NMS)
131. SEVERE CMT TYPE 2 WITH FATAL ENCEPHALOPATHY ASSOCIATED WITH A NOVEL MFN2 SPLICING MUTATION
132. OC.08.5 NEUROLOGICAL ABNORMALITIES IN PATIENTS WITH CHRONIC INTESTINAL PSEUDO-OBSTRUCTION
133. P-9 Construction of a database for a nation-wide Italian collaborative network of mitochondrial diseases
134. Novel quaternary ammonium chitosan derivatives for the promotion of intraocular drug absorption
135. Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy
136. Myelin, mitochondria, and autoimmunity: What's the connection?
137. OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
138. Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus
139. A Novel Polyelectrolyte Complex (PEC) Hydrogel for Controlled Drug Delivery to the Distal Intestine
140. G.P.18.05 Myopathy and retinopathy are novel features in a patient with Mohr-Tranebjaerg syndrome
141. M.P.1.14 Asymptomatic mitochondrial myopathy with mtDNA multiple deletions revealed by propofol-induced multiple organ failure with rhabdomyolysis
142. Visual evoked potentials (VEP) and brainstem evoked potentials (BAEP) as diagnostic procedures in Leber’s hereditary optic neuropathy
143. Colpocephaly in two siblings: further evidence of a genetic transmission
144. Dispersion of drugs in polymer networks by the solution impregnation method: criteria for control of loading dose
145. Vehicle influence on the permeation of a highly lipophilic molecule. An in vitro technique to evaluate skin-vehicle interactions
146. The ND1 gene of complex I is a mutational hot spot for Leber’s hereditary optic neuropathy
147. Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy
148. Design and in vitro evaluation of an extended-release matrix tablet for once-daily oral administration of oxybutynin
149. POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness
150. Optic nerve degeneration and mitochondrial dysfunction: genetic and acquired optic neuropathies
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