Resultados da pesquisa - Quinzii, Catarina M. 

Coenzyme Q and Mitochondrial Disease Por Quinzii, Catarina M., Hirano, Michio

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Primary and secondary CoQ(10) deficiencies in humans Por Quinzii, Catarina M., Hirano, Michio

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Redefining infantile-onset multisystem phenotypes of coenzyme Q(10)-deficiency in the next-generation sequencing era Por Berardo, Andres, Quinzii, Catarina M.

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Coenzyme Q10 as a Peripheral Biomarker for Multiple System Atrophy Por Kuo, Sheng-Han, Quinzii, Catarina M.

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Abnormalities of hydrogen sulfide and glutathione pathways in mitochondrial dysfunction Por Quinzii, Catarina M, Lopez, Luis C

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CoQ(10) deficiencies and MNGIE: Two Treatable Mitochondrial Disorders Por Hirano, Michio, Garone, Caterine, Quinzii, Catarina M.

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Clinical Presentations of Coenzyme Q(10) Deficiency Syndrome Por Quinzii, Catarina M., Emmanuele, Valentina, Hirano, Michio

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Cerebellar Ataxia and CoQ10 Deficiency Por Quinzii, Catarina M, Hirano, Michio, Naini, Ali

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Emerging Therapies for Mitochondrial Diseases Por Hirano, Michio, Emmanuele, Valentina, Quinzii, Catarina M

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Mutations in coenzyme Q(10) biosynthetic genes Por DiMauro, Salvatore, Quinzii, Catarina M., Hirano, Michio

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Human Coenzyme Q(10) Deficiency Por Quinzii, Catarina M., DiMauro, Salvatore, Hirano, Michio

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CoQ(10) deficiency diseases in adults Por Quinzii, Catarina M., Hirano, Michio, DiMauro, Salvatore

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Mutant COQ2 in Multiple-System Atrophy Por Quinzii, Catarina M., Hirano, Michio, DiMauro, Salvatore

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Mechanisms and Therapeutic Effects of Benzoquinone Ring Analogs in Primary CoQ Deficiencies Por Pesini, Alba, Hidalgo-Gutierrez, Agustin, Quinzii, Catarina M.

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Effects of Inhibiting CoQ(10) Biosynthesis with 4-nitrobenzoate in Human Fibroblasts Por Quinzii, Catarina M., Tadesse, Saba, Naini, Ali, Hirano, Michio

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Anti-Oxidant Drugs: Novelties and Clinical Implications in Cerebellar Ataxias Por Barca, Emanuele, Emmanuele, Valentina, DiMauro, Salvatore, Toscano, Antonio, Quinzii, Catarina M.

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Pathomechanisms in Coenzyme Q(10)-Deficient Human Fibroblasts Por López, Luis C., Luna-Sánchez, Marta, García-Corzo, Laura, Quinzii, Catarina M., Hirano, Michio

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Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice Por Quinzii, Catarina M., Garone, Caterina, Emmanuele, Valentina, Tadesse, Saba, Krishna, Sindu, Dorado, Beatriz, Hirano, Michio

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The Role of Sulfide Oxidation Impairment in the Pathogenesis of Primary CoQ Deficiency Por Quinzii, Catarina M., Luna-Sanchez, Marta, Ziosi, Marcello, Hidalgo-Gutierrez, Agustin, Kleiner, Giulio, Lopez, Luis C.

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A novel SUCLA2 mutation presenting as a complex childhood movement disorder Por Garone, Caterina, Gurgel-Giannetti, Juliana, Sanna-Cherchi, Simone, Krishna, Sindu, Naini, Ali, Quinzii, Catarina M, Hirano, Michio

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