Hasil Pencarian - Salvatore Dimauro

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  1. 1
    A Brief History of Mitochondrial Pathologies

    A Brief History of Mitochondrial Pathologies oleh Salvatore DiMauro

    Diterbitkan 2019-11-01
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  2. 2
    Miopatia por deficiência de succinato-citocromo-C-redutase: possível defeito no complexo II da cadeia respiratória

    Miopatia por deficiência de succinato-citocromo-C-redutase: possível defeito no complexo II da cadeia respiratória oleh Lineu Cesar Werneck, Salvatore DiMauro

    Diterbitkan 1989-12-01
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  3. 3
    Microanalysis of cardiolipin in small biopsies including skeletal muscle from patients with mitochondrial disease

    Microanalysis of cardiolipin in small biopsies including skeletal muscle from patients with mitochondrial disease oleh Michael Schlame, Sara Shanske, Steven Doty, Thomas König, Thomas Sculco, Salvatore DiMauro, Thomas J.J. Blanck

    Diterbitkan 1999-09-01
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  4. 4
    Treatment of CoQ(10) deficient fibroblasts with ubiquinone, CoQ analogs, and vitamin C: time- and compound-dependent effects.

    Treatment of CoQ(10) deficient fibroblasts with ubiquinone, CoQ analogs, and vitamin C: time- and compound-dependent effects. oleh Luis C López, Catarina M Quinzii, Estela Area, Ali Naini, Shamima Rahman, Markus Schuelke, Leonardo Salviati, Salvatore Dimauro, Michio Hirano

    Diterbitkan 2010-07-01
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  5. 5
    A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck.

    A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck. oleh Francesco Pallotti, Giorgio Binelli, Raffaella Fabbri, Maria L Valentino, Rossella Vicenti, Maria Macciocca, Sabina Cevoli, Agostino Baruzzi, Salvatore DiMauro, Valerio Carelli

    Diterbitkan 2014-01-01
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  6. 6
    Mitochondrial myopathy and myoclonic epilepsy

    Mitochondrial myopathy and myoclonic epilepsy oleh Walter O. Arruda, Luiz F. B. Torres, Anne lombes, Salvatore Dimauro, Belkiss A. Cardoso, Hélio A. G. Teive, Duilton de Paola, Ricardo R. Seixas

    Diterbitkan 1990-03-01
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  7. 7
    Visual memory failure presages conversion to MELAS phenotype

    Visual memory failure presages conversion to MELAS phenotype oleh Emily B. Leaffer, Darryl C. De Vivo, Kristin Engelstad, Robert H. Fryer, Yian Gu, Dikoma C. Shungu, Michio Hirano, Salvatore DiMauro, Veronica J. Hinton

    Diterbitkan 2022-06-01
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  8. 8
    Mitochondrial abnormalities in temporal lobe of autistic brain

    Mitochondrial abnormalities in temporal lobe of autistic brain oleh Guomei Tang, Puri Gutierrez Rios, Sheng-Han Kuo, Hasan Orhan Akman, Gorazd Rosoklija, Kurenai Tanji, Andrew Dwork, Eric A. Schon, Salvatore DiMauro, James Goldman, David Sulzer

    Diterbitkan 2013-06-01
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  9. 9
    Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy.

    Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy. oleh Karen M Vernau, Jonathan A Runstadler, Emily A Brown, Jessie M Cameron, Heather J Huson, Robert J Higgins, Cameron Ackerley, Beverly K Sturges, Peter J Dickinson, Birgit Puschner, Cecilia Giulivi, G Diane Shelton, Brian H Robinson, Salvatore DiMauro, Andrew W Bollen, Danika L Bannasch

    Diterbitkan 2013-01-01
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