檢索結果

在您的搜尋 主題建議
Refine Results
  1. 1
    Mitochondrial diseases and epilepsy

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

    出版 2012
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  2. 2
    Mitochondrial myopathy and myoclonic epilepsy

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

    出版 1990
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  3. 3
    Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes

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

    出版 2015
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  4. 4
    Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy

    Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy 由 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

    出版 2015
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  5. 5
    A novel diagnostic tool reveals mitochondrial pathology in human diseases and aging

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

    出版 2013
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  6. 6
    Clinical and biochemical improvements in a patient with MNGIE following enzyme replacement

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

    出版 2013
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  7. 7
    The optic nerve: A “mito-window” on mitochondrial neurodegeneration

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

    出版 2012
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  8. 8
    Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy

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

    出版 2011
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  9. 9
    Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathy.

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

    出版 1995
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  10. 10
    Liver as a Source for Thymidine Phosphorylase Replacement in Mitochondrial Neurogastrointestinal Encephalomyopathy

    Liver as a Source for Thymidine Phosphorylase Replacement in Mitochondrial Neurogastrointestinal Encephalomyopathy 由 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

    出版 2014
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  11. 11
    Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy

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

    出版 2014
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  12. 12
    Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers

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

    出版 2014
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  13. 13
    Cytochrome c oxidase deficiency: Patients and animal models

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

    出版 2009
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  14. 14
    Mice with Mitochondrial Complex I Deficiency Develop a Fatal Encephalomyopathy

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

    出版 2008
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  15. 15
    Recovery of MERRF Fibroblasts and Cybrids Pathophysiology by Coenzyme Q10

    Recovery of MERRF Fibroblasts and Cybrids Pathophysiology by Coenzyme Q10 由 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

    出版 2012
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  16. 16
    Determination of Coenzyme Q10 Status in Blood Mononuclear Cells, Skeletal Muscle, and Plasma by HPLC with Di-Propoxy-Coenzyme Q10 as an Internal Standard

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

    出版 2005
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  17. 17
    Identification of a Novel Mutation in the mtDNA ND5 Gene Associated with MELAS

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

    出版 1997
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  18. 18
    Mitochondrial dysfunction in neurodegenerative diseases

    Mitochondrial dysfunction in neurodegenerative diseases 由 M. Flint Beal

    出版 1998
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  19. 19
    Mitochondrial DNA deletion: A cause of chronic tubulointerstitial nephropathy

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

    出版 1994
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  20. 20
    Mutations in coenzyme Q10 biosynthetic genes

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

    出版 2007
    獲取全文 獲取全文
    Carta
    加到收藏夾
    Saved in:

檢索工具: