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Results: 1-25 | 26-36
Results: 1-25/36
A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathy
Authors: Karadimas, C Tanji, K Geremek, M Chronopoulou, P Vu, T Krishna, S Sue, CM Shanske, S Bonilla, E DiMauro, S Lipson, M Bachman, R
Citation: C. Karadimas et al., A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathy, J CHILD NEU, 16(7), 2001, pp. 531-533
Melatonin treatment enhances the efficiency of mice immunization with Venezuelan equine encephalomyelitis virus TC-83
Authors: Negrette, B Bonilla, E Valero, N Pons, H Tamayo, JG Chacin-Bonilla, L Medina-Leendertz, S Anez, F
Citation: B. Negrette et al., Melatonin treatment enhances the efficiency of mice immunization with Venezuelan equine encephalomyelitis virus TC-83, NEUROCHEM R, 26(7), 2001, pp. 767-770
High intensity light increases olfactory bulb melatonin in venezuelan equine encephalitis virus infection
Authors: Medina-Leendertz, S Valero, N Chacin-Bonilla, L Anez, F Giraldoth, D Arias, J Espina, G Diaz, S Bonilla, E
Citation: S. Medina-leendertz et al., High intensity light increases olfactory bulb melatonin in venezuelan equine encephalitis virus infection, NEUROCHEM R, 26(3), 2001, pp. 231-234
Effect of chronic manganese treatment on adenosine tissue levels and adenosine A(2a) receptor binding in diverse regions of mouse brain
Authors: Villalobos, V Suarez, J Estevez, J Novo, E Bonilla, E
Citation: V. Villalobos et al., Effect of chronic manganese treatment on adenosine tissue levels and adenosine A(2a) receptor binding in diverse regions of mouse brain, NEUROCHEM R, 26(10), 2001, pp. 1157-1161
Diseases of oxidative phosphorylation due to mtDNA mutations
Authors: DiMauro, S Andreu, AL Musumeci, O Bonilla, E
Citation: S. Dimauro et al., Diseases of oxidative phosphorylation due to mtDNA mutations, SEM NEUROL, 21(3), 2001, pp. 251-260
Navajo neurohepatopathy: A mitochondrial DNA depletion syndrome?
Authors: Vu, TH Tanji, K Holve, SA Bonilla, E Sokol, RJ Snyder, RD Fiore, S Deutsch, GH DiMauro, S De Vivo, D
Citation: Th. Vu et al., Navajo neurohepatopathy: A mitochondrial DNA depletion syndrome?, HEPATOLOGY, 34(1), 2001, pp. 116-120
Optical imaging techniques (Histochemical, immunohistochemical, and in situ hybridization staining methods) to visualize mitochondria
Authors: Tanji, K Bonilla, E
Citation: K. Tanji et E. Bonilla, Optical imaging techniques (Histochemical, immunohistochemical, and in situ hybridization staining methods) to visualize mitochondria, METH CELL B, 65, 2001, pp. 311
Melatonin prolongs survival of immunodepressed mice infected with the Venezuelan equine encephalomyelitis virus
Authors: Bonilla, E Rodon, C Valero, N Pons, H Chacin-Bonilla, L Tamayo, JG Rodriguez, Z Medina-Leendertz, S Anez, F
Citation: E. Bonilla et al., Melatonin prolongs survival of immunodepressed mice infected with the Venezuelan equine encephalomyelitis virus, T RS TROP M, 95(2), 2001, pp. 207-210
Myopathy with tubulin-reactive crystalline inclusions
Authors: Vu, TH Hays, AP Tanji, K Younger, D Gundersen, GG Eastwood, A Braun, CW DiMauro, S Bonilla, E
Citation: Th. Vu et al., Myopathy with tubulin-reactive crystalline inclusions, NEUROLOGY, 57(1), 2001, pp. 149-152
Neuropathologic aspects of cytochrome C oxidase deficiency
Authors: Tanji, K Bonilla, E
Citation: K. Tanji et E. Bonilla, Neuropathologic aspects of cytochrome C oxidase deficiency, BRAIN PATH, 10(3), 2000, pp. 422-430
Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
Authors: Nishino, I Spinazzola, A Papadimitriou, A Hammans, S Steiner, I Hahn, CD Connolly, AM Verloes, A Guimaraes, J Maillard, I Hamano, H Donati, MA Semrad, CE Russell, JA Andreu, AL Hadjigeorgiou, GM Vu, TH Tadesse, S Nygaard, TG Nonaka, I Hirano, I Bonilla, E Rowland, LP DiMauro, S Hirano, M
Citation: I. Nishino et al., Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations, ANN NEUROL, 47(6), 2000, pp. 792-800
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2
Authors: Sue, CM Karadimas, C Checcarelli, N Tanji, K Papadopoulou, LC Pallotti, F Guo, FL Shanske, S Hirano, M De Vivo, DC Van Coster, R Kaplan, P Bonilla, E DiMauro, S
Citation: Cm. Sue et al., Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2, ANN NEUROL, 47(5), 2000, pp. 589-595
Analysis of mtDNA deletions in muscle by in situ hybridization
Authors: Vu, TH Tanji, K Pallotti, F Golzi, V Hirano, M DiMauro, S Bonilla, E
Citation: Th. Vu et al., Analysis of mtDNA deletions in muscle by in situ hybridization, MUSCLE NERV, 23(1), 2000, pp. 80-85
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA
Authors: Karadimas, CL Greenstein, P Sue, CM Joseph, JT Tanji, K Haller, RG Taivassalo, T Davidson, MM Shanske, S Bonilla, E DiMauro, S
Citation: Cl. Karadimas et al., Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA, NEUROLOGY, 55(5), 2000, pp. 644-649
Mitochondrial analysis in autosomal dominant hereditary spastic paraplegia
Authors: Hedera, P DiMauro, S Bonilla, E Wald, JJ Fink, JK
Citation: P. Hedera et al., Mitochondrial analysis in autosomal dominant hereditary spastic paraplegia, NEUROLOGY, 55(10), 2000, pp. 1591-1592
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
Authors: Nishino, I Fu, J Tanji, K Yamada, T Shimojo, S Koori, T Mora, M Riggs, JE Oh, SJ Koga, Y Sue, CM Yamamoto, A Murakami, N Shanske, S Byrne, E Bonilla, E Nonaka, I DiMauro, S Hirano, M
Citation: I. Nishino et al., Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease), NATURE, 406(6798), 2000, pp. 906-910
Kearns-Sayre syndrome: oncocytic transformation of choroid plexus epithelium
Authors: Tanji, K Schon, EA DiMauro, S Bonilla, E
Citation: K. Tanji et al., Kearns-Sayre syndrome: oncocytic transformation of choroid plexus epithelium, J NEUR SCI, 178(1), 2000, pp. 29-36
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
Authors: Papadopoulou, LC Sue, CM Davidson, MM Tanji, K Nishino, I Sadlock, JE Krishna, S Walker, W Selby, J Glerum, DM Van Coster, R Lyon, G Scalais, E Lebel, R Kaplan, P Shanske, S De Vivo, DC Bonilla, E Hirano, M DiMauro, S Schon, EA
Citation: Lc. Papadopoulou et al., Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene, NAT GENET, 23(3), 1999, pp. 333-337
Does the patient have a mitochondrial encephalomyopathy?
Authors: DiMauro, S Bonilla, E De Vivo, DC
Citation: S. Dimauro et al., Does the patient have a mitochondrial encephalomyopathy?, J CHILD NEU, 14, 1999, pp. S23-S35
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene
Authors: Andreu, AL Tanji, K Bruno, C Hadjigeorgiou, GM Sue, CM Jay, C Ohnishi, T Shanske, S Bonilla, E DiMauro, S
Citation: Al. Andreu et al., Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene, ANN NEUROL, 45(6), 1999, pp. 820-823
Kearns-Sayre syndrome: Unusual pattern of expression of subunits of the respiratory chain in the cerebellar system
Authors: Tanji, K Vu, TH Schon, EA DiMauro, S Bonilla, E
Citation: K. Tanji et al., Kearns-Sayre syndrome: Unusual pattern of expression of subunits of the respiratory chain in the cerebellar system, ANN NEUROL, 45(3), 1999, pp. 377-383
A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria
Authors: Andreu, AL Bruno, C Dunne, TC Tanji, K Shanske, S Sue, CM Krishna, S Hadjigeorgiou, GM Shtilbans, A Bonilla, E DiMauro, S
Citation: Al. Andreu et al., A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria, ANN NEUROL, 45(1), 1999, pp. 127-130
Exposure to 2500 lux increases serum melatonin in venezuelan equine encephalomyelitis
Authors: Medina, S Valero-Fuenmayor, N Chacin-Bonilla, L Anez, F Giraldoth, D Arias, J Espina, G Achong, AY Bonilla, E
Citation: S. Medina et al., Exposure to 2500 lux increases serum melatonin in venezuelan equine encephalomyelitis, NEUROCHEM R, 24(6), 1999, pp. 775-778
Decrease in spontaneous motor activity and in brain lipid peroxidation in manganese and melatonin treated mice
Authors: Talavera, EJ Arcaya, JL Giraldoth, D Suarez, J Bonilla, E
Citation: Ej. Talavera et al., Decrease in spontaneous motor activity and in brain lipid peroxidation in manganese and melatonin treated mice, NEUROCHEM R, 24(5), 1999, pp. 705-708
Reduced tolerance and cardiovascular response to ischemic pain in minor depression
Authors: Pinerua-Shuhaibar, L Prieto-Rincon, D Ferrer, A Bonilla, E Maixner, W Suarez-Roca, H
Citation: L. Pinerua-shuhaibar et al., Reduced tolerance and cardiovascular response to ischemic pain in minor depression, J AFFECT D, 56(2-3), 1999, pp. 119-126
Risultati: 1-25 | 26-36