antonio federico
antonio federico
professore ordinario università di siena
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Cited by
Cited by
Accurate, robust, and automated longitudinal and cross-sectional brain change analysis
SM Smith, Y Zhang, M Jenkinson, J Chen, PM Matthews, A Federico, ...
Neuroimage 17 (1), 479-489, 2002
Mitochondria, oxidative stress and neurodegeneration
A Federico, E Cardaioli, P Da Pozzo, P Formichi, GN Gallus, E Radi
Journal of the neurological sciences 322 (1-2), 254-262, 2012
Apoptosis and oxidative stress in neurodegenerative diseases
E Radi, P Formichi, C Battisti, A Federico
Journal of Alzheimer's disease 42 (s3), S125-S152, 2014
Evidence of early cortical atrophy in MS: relevance to white matter changes and disability
N De Stefano, PM Matthews, M Filippi, F Agosta, M De Luca, ...
Neurology 60 (7), 1157-1162, 2003
Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease
M Quadri, A Federico, T Zhao, GJ Breedveld, C Battisti, C Delnooz, ...
The American Journal of Human Genetics 90 (3), 467-477, 2012
Neocortical volume decrease in relapsing–remitting MS patients with mild cognitive impairment
MP Amato, ML Bartolozzi, V Zipoli, E Portaccio, M Mortilla, L Guidi, ...
Neurology 63 (1), 89-93, 2004
Association of neocortical volume changes with cognitive deterioration in relapsing-remitting multiple sclerosis
MP Amato, E Portaccio, B Goretti, V Zipoli, M Battaglini, ML Bartolozzi, ...
Archives of neurology 64 (8), 1157-1161, 2007
MECP2 mutation in male patients with non-specific X-linked mental retardation
A Orrico, CW Lam, L Galli, MT Dotti, G Hayek, SF Tong, PMK Poon, ...
FEBS letters 481 (3), 285-288, 2000
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and …
I Di Donato, S Bianchi, N De Stefano, M Dichgans, MT Dotti, M Duering, ...
BMC medicine 15, 1-12, 2017
Transcriptome profiling in human diseases: new advances and perspectives
A Casamassimi, A Federico, M Rienzo, S Esposito, A Ciccodicola
International journal of molecular sciences 18 (8), 1652, 2017
Blood oxygenation level dependent contrast resting state networks are relevant to functional activity in the neocortical sensorimotor system
M De Luca, S Smith, N De Stefano, A Federico, PM Matthews
Experimental brain research 167, 587-594, 2005
Unstable insertion in the 5′ flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1
RG Lafreniére, DL Rochefort, N Chrétien, JM Rommens, JI Cochius, ...
Nature genetics 15 (3), 298-302, 1997
Diffuse axonal and tissue injury in patients with multiple sclerosis with low cerebral lesion load and no disability
N De Stefano, S Narayanan, SJ Francis, S Smith, M Mortilla, MC Tartaglia, ...
Archives of neurology 59 (10), 1565-1571, 2002
Clinical and molecular diagnosis of cerebrotendinous xanthomatosis with a review of the mutations in the CYP27A1 gene
GN Gallus, MT Dotti, A Federico
Neurological Sciences 27, 143-149, 2006
A system oriented integrated indicator for sustainable development in Italy
E Ronchi, A Federico, F Musmeci
Ecological Indicators 2 (1-2), 197-210, 2002
Cerebrotendinous xanthomatosis: clinical manifestations, diagnostic criteria, pathogenesis, and therapy
A Federico, MT Dotti
Journal of child neurology 18 (9), 633-638, 2003
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis
C Dobson-Stone, A Danek, L Rampoldi, RJ Hardie, RM Chalmers, ...
European Journal of Human Genetics 10 (11), 773-781, 2002
Chorein detection for the diagnosis of chorea‐acanthocytosis
C Dobson‐Stone, A Velayos‐Baeza, LA Filippone, S Westbury, A Storch, ...
Annals of Neurology: Official Journal of the American Neurological …, 2004
Magnetic resonance imaging and spectroscopic changes in brains of patients with cerebrotendinous xanthomatosis
N De Stefano, MT Dotti, M Mortilla, A Federico
Brain 124 (1), 121-131, 2001
Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy
A Orr, MP Dube, J Marcadier, H Jiang, A Federico, S George, C Seamone, ...
PLoS One 2 (8), e685, 2007
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