Suchergebnisse - "Garone, Caterina"

PubPharm (4)

1

A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder

enthalten in: Journal of child neurology | 2017

von Garone, C. | Gurgel-Giannetti, J. | Sanna-Cherchi, S. | +4

2

Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia

enthalten in: Proceedings of the National Academy of Sciences of the United States of America | 2013

von Manoli, I. | Sysol, J. | Li, L. | +20

3

Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice

enthalten in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2013

von Quinzii, C. | Garone, C. | Emmanuele, V. | +4

4

CoQ(10) deficiencies and MNGIE : two treatable mitochondrial disorders

enthalten in: Biochimica et biophysica acta | 2012

von Hirano, M. | Garone, C. | Quinzii, C.

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