Dotti, Maria Teresa

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

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

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

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

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

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

Liver transplantation in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical long-term follow-up and pathogenic implications

D’Angelo, R., Boschetti, E., Amore, G., Costa, R., Pugliese, A., Caporali, L., Gramegna, L. L., Papa, V., Vizioli, L., Capristo, M., et al. (2020) · Journal of Neurology

Mitochondrial Function and PathologyMetabolism and Genetic Disorders

Cited by 29