Suchergebnisse - "Garone, Caterina"

PubPharm (120)

81

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

82

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

83

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

Erschienen: 2013

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

84

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

enthalten in: The FASEB Journal | 2013

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

85

MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA Deletions

enthalten in: Archives of neurology | 2012

von Garone, C. | Rubio, J. | Calvo, S. | +5

86

Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions

enthalten in: Brain : a journal of neurology | 2012

von Ronchi, D. | Garone, C. | Bordoni, A. | +14

CommentIn: Brain. 2018 Jan 1;141(1):e3. - PMID 29228108

87

Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions

enthalten in: Brain | 2012

von Ronchi, D. | Garone, C. | Bordoni, A. | +14

88

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

enthalten in: Biochimica et biophysica acta | 2012

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

89

CoQ10 deficiencies and MNGIE: Two treatable mitochondrial disorders

enthalten in: Biochimica et biophysica acta / General subjects | 2012

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

90

Fever as a seizure precipitant factor in Panayiotopoulos syndrome : a clinical and genetic study

enthalten in: Seizure | 2012

von Cordelli, D. | Aldrovandi, A. | Gentile, V. | +6