Gaetano Vattemi

Summary

Affiliation: University of Verona
Country: Italy

Publications

  1. doi request reprint Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria
    Gaetano Vattemi
    Section of Clinical Neurology, Department of Neurological, Neuropsychological, Morphological, and Movement Sciences, University of Verona, 37134 Verona, Italy
    Free Radic Biol Med 63:108-14. 2013
  2. doi request reprint Brody disease: insights into biochemical features of SERCA1 and identification of a novel mutation
    Gaetano Vattemi
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Verona, Italy
    J Neuropathol Exp Neurol 69:246-52. 2010
  3. pmc Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy
    G Vattemi
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Italy
    Acta Myol 30:121-6. 2011
  4. ncbi request reprint SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy
    Giuliano Tomelleri
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Verona, Italy
    Brain 129:2085-92. 2006
  5. doi request reprint Endothelial dysfunction and increased oxidative stress in mitochondrial diseases
    Pietro Minuz
    Department of Medicine, Section of Internal Medicine, University of Verona, Verona, Italy
    Clin Sci (Lond) 122:289-97. 2012
  6. doi request reprint Novel mitochondrial tRNA Leu(CUN) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype
    Massimiliano Filosto
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Italy
    Neuromuscul Disord 18:204-9. 2008
  7. doi request reprint Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency
    Gaetano Vattemi
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Verona, Italy
    Neurologist 18:306-9. 2012
  8. pmc Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement
    Gaetano Vattemi
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Italy
    Mol Cell Proteomics 10:M110.002964. 2011
  9. ncbi request reprint Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases
    Massimiliano Filosto
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Policlinico G B Rossi, P le L A Scuro 10, 37134 Verona, Italy
    Acta Neuropathol 103:215-20. 2002
  10. doi request reprint SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers
    Valeria Guglielmi
    Department of Neurological, Neuropsychological, Morphological and Movement Sciences, Section of Clinical Neurology, University of Verona, Italy
    Mol Genet Metab 110:162-9. 2013

Collaborators

Detail Information

Publications10

  1. doi request reprint Overexpression of TNF-α in mitochondrial diseases caused by mutations in mtDNA: evidence for signaling through its receptors on mitochondria
    Gaetano Vattemi
    Section of Clinical Neurology, Department of Neurological, Neuropsychological, Morphological, and Movement Sciences, University of Verona, 37134 Verona, Italy
    Free Radic Biol Med 63:108-14. 2013
    ..These findings suggest for the first time that TNF-α could exert a direct effect on mitochondria via its receptors. ..
  2. doi request reprint Brody disease: insights into biochemical features of SERCA1 and identification of a novel mutation
    Gaetano Vattemi
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Verona, Italy
    J Neuropathol Exp Neurol 69:246-52. 2010
    ..In addition, we describe 2 novel mutations in the ATP2A1 gene...
  3. pmc Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy
    G Vattemi
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Italy
    Acta Myol 30:121-6. 2011
    ....
  4. ncbi request reprint SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy
    Giuliano Tomelleri
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Verona, Italy
    Brain 129:2085-92. 2006
    ..Our cases, both sporadic and familial, represent a new type of surplus protein myopathy...
  5. doi request reprint Endothelial dysfunction and increased oxidative stress in mitochondrial diseases
    Pietro Minuz
    Department of Medicine, Section of Internal Medicine, University of Verona, Verona, Italy
    Clin Sci (Lond) 122:289-97. 2012
    ..58±0.30%), thus abolishing the differences between patients and controls. The results of the present study indicate that oxidative stress is increased and is, at least partly, responsible for endothelial dysfunction in MDs...
  6. doi request reprint Novel mitochondrial tRNA Leu(CUN) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype
    Massimiliano Filosto
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Italy
    Neuromuscul Disord 18:204-9. 2008
    ..This is the first reported case of mitochondrial myopathy/facioscapulohumeral muscular dystrophy (FSHD) "double trouble"...
  7. doi request reprint Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency
    Gaetano Vattemi
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Verona, Italy
    Neurologist 18:306-9. 2012
    ..Nevertheless, calpainopathy is not always associated with mutations in the specific gene and secondary reduction in protein expression has been described...
  8. pmc Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement
    Gaetano Vattemi
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Italy
    Mol Cell Proteomics 10:M110.002964. 2011
    ..The present results provide evidence that in MD the vessel wall is a target of increased oxidative/nitrative stress...
  9. ncbi request reprint Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases
    Massimiliano Filosto
    Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Policlinico G B Rossi, P le L A Scuro 10, 37134 Verona, Italy
    Acta Neuropathol 103:215-20. 2002
    ..In addition, we suggest that expression of MnSOD and GSH may be considered an initial, indirect sign of respiratory chain dysfunction because it is observed in the early stages of the disease...
  10. doi request reprint SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers
    Valeria Guglielmi
    Department of Neurological, Neuropsychological, Morphological and Movement Sciences, Section of Clinical Neurology, University of Verona, Italy
    Mol Genet Metab 110:162-9. 2013
    ..Finally, we identified two novel heterozygous mutations within exon 3 of the ATP2A1 gene from a previously described patient with BD. ..