Federico, Antonio
University of Siena
9 papers on CoChatORCID 0000-0002-5246-1621
Most cited papers
- Verified
The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1-6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7-34 pathogenic variant
Rutten, J. W., Van Eijsden, B. J., Duering, M., Jouvent, E., Opherk, C., Pantoni, L., Federico, A., Dichgans, M., Markus, H. S., Chabriat, H., et al. (2019) · Genetics in Medicine
Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases
Cited by 169
- Verified
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study
D'Amore, A., Tessa, A., Casali, C., Dotti, M. T., Filla, A., Silvestri, G., Antenora, A., Astrea, G., Barghigiani, M., Battini, R., et al. (2018) · Frontiers in Neurology
Hereditary Neurological DisordersGenomics and Rare Diseases
Cited by 90
- Verified
Hereditary cerebral small vessel diseases: a review
Federico, A., Di Donato, I., Bianchi, S., Di Palma, C., Taglia, I., & Dotti, M. T. (2012) · Journal of the Neurological Sciences
Cerebrovascular and genetic disordersNeurological Disease Mechanisms and Treatments
Cited by 82
- Verified
Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3 -negative patients
Pantoni, L., Pescini, F., Nannucci, S., Sarti, C., Bianchi, S., Dotti, M. T., Federico, A., & Inzitari, D. (2010) · Neurology
Cerebrovascular and genetic disordersMigraine and Headache Studies
Cited by 82
- Verified
Cortical lesions in radiologically isolated syndrome
Giorgio, A., Stromillo, M. L., Rossi, F., Battaglini, M., Hakiki, B., Portaccio, E., Federico, A., Amato, M. P., & De Stefano, N. (2011) · Neurology
Multiple Sclerosis Research StudiesAdvanced Neuroimaging Techniques and Applications
Cited by 77
- Verified
DIAGNOSTIC VALUE OF ULTRASTRUCTURAL SKIN BIOPSY STUDIES IN CADASIL
Malandrini, A., Gaudiano, C., Gambelli, S., Berti, G., Serni, G., Bianchi, S., Federico, A., & Dotti, M. T. (2007) · Neurology
Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases
Cited by 57
- Verified
Operationalizing mild cognitive impairment criteria in small vessel disease: the VMCI‐Tuscany Study
Salvadori, E., Poggesi, A., Valenti, R., Pracucci, G., Pescini, F., Pasi, M., Nannucci, S., Marini, S., Del Bene, A., Ciolli, L., et al. (2016) · Alzheimer's & Dementia
Dementia and Cognitive Impairment ResearchNeurological Disease Mechanisms and Treatments
Cited by 36
- Verified
Plasma levels of asymmetric dimethylarginine in cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathy
Rufa, A., Blardi, P., De Lalla, A., Cevenini, G., De Stefano, N., Zicari, E., Auteri, A., Federico, A., & Dotti, M. T. (2008) · Cerebrovascular Diseases
Cerebrovascular and genetic disordersNitric Oxide and Endothelin Effects
Cited by 31
- Verified
Clinical, familial, and neuroimaging features of CADASIL‐like patients
Nannucci, S., Pescini, F., Bertaccini, B., Bianchi, S., Ciolli, L., Valenti, R., Dotti, M. T., Federico, A., Inzitari, D., & Pantoni, L. (2015) · Acta Neurologica Scandinavica
Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases
Cited by 16
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