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Mitochondrial diseases and epilepsy Por Laurence A. Bindoff, Bernt A. Engelsen

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Mitochondrial myopathy and myoclonic epilepsy Por Walter O. Arruda, Luíz Fernando Bleggi Torres, Anne Lombès, Salvatore DiMauro, Belkiss A. Cardoso, Hélio Afonso Ghizoni Teive, Duilton de Paola, Ricardo R. Seixas

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Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Por Ying-Xin Wang, Wei-Dong Le

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Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy Por Joerg Halter, W. Michael, Michaël Schüpbach, Hanna Mandel, Carlo Casali, Kim Orchard, Matthew Collin, David Valcárcel, Attilio Rovelli, Massimiliano Filosto, Maria T. Dotti, Giuseppe Marotta, Guillem Pintos‐Morell, Pere Barba, Anna Accarino, Christelle Ferrà, Isabel Illa, Yves Béguin, Jaap Bakker, Jaap Jan Boelens, I.F.M. de Coo, Keith Fay, Carolyn M. Sue, David Nachbaur, Heinz Zoller, Cláudia Ferreira da Rosa Sobreira, Belinda Pinto Simões, Simon Hammans, David G. Savage, Ramón Martí, Patrick F. Chinnery, Ronit Elhasid, Aloïs Gratwohl, Michio Hirano

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A novel diagnostic tool reveals mitochondrial pathology in human diseases and aging Por Morten Scheibye‐Knudsen, Karsten Scheibye-Alsing, Chandrika Canugovi, Deborah L. Croteau, Vilhelm A. Bohr

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Clinical and biochemical improvements in a patient with MNGIE following enzyme replacement Por Bridget E. Bax, Murray Bain, Mauro Scarpelli, Massimiliano Filosto, Paola Tonin, Nicholas Moran

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The optic nerve: A “mito-window” on mitochondrial neurodegeneration Por Alessandra Maresca, Chiara La Morgia, Leonardo Caporali, Maria Lucia Valentino, Valério Carelli

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Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy Por Caterina Garone, Saba Tadesse, Michio Hirano

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Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathy. Por Anna M. Moudy, S D Handran, Mark P. Goldberg, Nicolas Ruffin, Irene E. Karl, Pamela Kranz‐Eble, D. C. DeVivo, Steven M. Rothman

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Liver as a Source for Thymidine Phosphorylase Replacement in Mitochondrial Neurogastrointestinal Encephalomyopathy Por Elisa Boschetti, Roberto D’Alessandro, Francesca Bianco, Valério Carelli, Giovanna Cenacchi, Antonio D. Pinna, Massimo Del Gaudio, Rita Rinaldi, Vincenzo Stanghellini, Loris Pironi, Kerry J. Rhoden, Vitaliano Tugnoli, Carlo Casali, Roberto De Giorgio

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Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy Por Ulla Najwa Abdulhag, Devorah Soiferman, Ora Schueler‐Furman, Chaya Miller, Avraham Shaag, Orly Elpeleg, Simon Edvardson, Ann Saada

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Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers Por Nora Weiduschat, Petra Kaufmann, Xiangling Mao, Kristin Engelstad, Veronica J. Hinton, Salvatore DiMauro, Darryl C. De Vivo, Dikoma C. Shungu

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Cytochrome c oxidase deficiency: Patients and animal models Por Francisca Díaz

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Mice with Mitochondrial Complex I Deficiency Develop a Fatal Encephalomyopathy Por Shane E. Kruse, W. C. Watt, David J. Marcinek, Raj P. Kapur, Kenneth A. Schenkman, Richard D. Palmiter

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Recovery of MERRF Fibroblasts and Cybrids Pathophysiology by Coenzyme Q10 Por Mario de la Mata, Juan Garrido‐Maraver, David Cotán, Mario D. Cordero, Manuel Oropesa-Ávila, Lourdes Gómez Izquierdo, Manuel de Miguel, Juan Bautista Lorite, Eloy Rivas, Patricia Ybot‐González, Sandra L. Jackson, José A. Sánchez‐Alcázar

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Determination of Coenzyme Q10 Status in Blood Mononuclear Cells, Skeletal Muscle, and Plasma by HPLC with Di-Propoxy-Coenzyme Q10 as an Internal Standard Por Andrew Duncan, Simon Heales, Kevin Mills, Simon Eaton, John M. Land, Iain P. Hargreaves

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Identification of a Novel Mutation in the mtDNA ND5 Gene Associated with MELAS Por Filippo M. Santorelli, Kurenai Tanji, Romana Kulikova, Sara Shanske, Laura Vilarinho, Arthur P. Hays, Salvatore DiMauro

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Mitochondrial dysfunction in neurodegenerative diseases Por M. Flint Beal

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Mitochondrial DNA deletion: A cause of chronic tubulointerstitial nephropathy Por Matthias J. Szabolcs, Robert L. Seigle, Sarah Shanske, E. Bonilla, S. DiMauro, Vivette D. D’Agati

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Mutations in coenzyme Q10 biosynthetic genes Por Salvatore DiMauro, Catarina M. Quinzii, Michio Hirano

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