Ohcanbohtosat - Quinzii, Catarina M.
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Coenzyme Q and Mitochondrial Disease Dahkki Quinzii, Catarina M., Hirano, Michio
Almmustuhtton 2010Teaksta -
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Primary and secondary CoQ(10) deficiencies in humans Dahkki Quinzii, Catarina M., Hirano, Michio
Almmustuhtton 2011Teaksta -
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Coenzyme Q10 as a Peripheral Biomarker for Multiple System Atrophy Dahkki Kuo, Sheng-Han, Quinzii, Catarina M.
Almmustuhtton 2016Teaksta -
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Cerebellar Ataxia and CoQ10 Deficiency Dahkki Quinzii, Catarina M, Hirano, Michio, Naini, Ali
Almmustuhtton 2013Teaksta -
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Emerging Therapies for Mitochondrial Diseases Dahkki Hirano, Michio, Emmanuele, Valentina, Quinzii, Catarina M
Almmustuhtton 2018Teaksta -
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Mutations in coenzyme Q(10) biosynthetic genes Dahkki DiMauro, Salvatore, Quinzii, Catarina M., Hirano, Michio
Almmustuhtton 2007Teaksta -
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Human Coenzyme Q(10) Deficiency Dahkki Quinzii, Catarina M., DiMauro, Salvatore, Hirano, Michio
Almmustuhtton 2006Teaksta -
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CoQ(10) deficiency diseases in adults Dahkki Quinzii, Catarina M., Hirano, Michio, DiMauro, Salvatore
Almmustuhtton 2007Teaksta -
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Mutant COQ2 in Multiple-System Atrophy Dahkki Quinzii, Catarina M., Hirano, Michio, DiMauro, Salvatore
Almmustuhtton 2014Teaksta -
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Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice Dahkki Quinzii, Catarina M., Garone, Caterina, Emmanuele, Valentina, Tadesse, Saba, Krishna, Sindu, Dorado, Beatriz, Hirano, Michio
Almmustuhtton 2013Teaksta -
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The Role of Sulfide Oxidation Impairment in the Pathogenesis of Primary CoQ Deficiency Dahkki Quinzii, Catarina M., Luna-Sanchez, Marta, Ziosi, Marcello, Hidalgo-Gutierrez, Agustin, Kleiner, Giulio, Lopez, Luis C.
Almmustuhtton 2017Teaksta -
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A novel SUCLA2 mutation presenting as a complex childhood movement disorder Dahkki Garone, Caterina, Gurgel-Giannetti, Juliana, Sanna-Cherchi, Simone, Krishna, Sindu, Naini, Ali, Quinzii, Catarina M, Hirano, Michio
Almmustuhtton 2016Teaksta