CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients von Bianchi, Silvia, Zicari, Enza, Carluccio, Alessandra, Di Donato, Ilaria, Pescini, Francesca, Nannucci, Serena, Valenti, Raffaella, Ragno, Michele, Inzitari, Domenico, Pantoni, Leonardo, Federico, Antonio, Dotti, Maria Teresa

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The Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale: A Screening Tool to Select Patients for NOTCH3 Gene Analysis von PESCINI, Francesca, NANNUCCI, Serena, CHITI, Stefano, STROMILLO, Maria Laura, DE STEFANO, Nicola, DOTTI, Maria Teresa, FEDERICO, Antonio, INZITARI, Domenico, PANTONI, Leonardo, BERTACCINI, Bruno, SALVADORI, Emilia, BIANCHI, Silvia, RAGNO, Michele, SARTI, Cristina, VALENTI, Raffaella, ZICARI, Enza, MORETTI, Marco

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The burden of microstructural damage modulates cortical activation in elderly subjects with MCI and leuko-araiosis. A DTI and fMRI study von Mascalchi, Mario, Ginestroni, Andrea, Toschi, Nicola, Poggesi, Anna, Cecchi, Paolo, Salvadori, Emilia, Tessa, Carlo, Cosottini, Mirco, De Stefano, Nicola, Pracucci, Giovanni, Pantoni, Leonardo, Inzitari, Domenico, Diciotti, Stefano

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Operationalizing mild cognitive impairment criteria in small vessel disease: the VMCI-Tuscany Study von Salvadori, Emilia, Poggesi, Anna, Valenti, Raffaella, Pracucci, Giovanni, Pescini, Francesca, Pasi, Marco, Nannucci, Serena, Marini, Sandro, Del Bene, Alessandra, Ciolli, Laura, Ginestroni, Andrea, Diciotti, Stefano, Orlandi, Giovanni, Di Donato, Ilaria, De Stefano, Nicola, Cosottini, Mirco, Chiti, Alberto, Federico, Antonio, Dotti, Maria Teresa, Bonuccelli, Ubaldo, Inzitari, Domenico, Pantoni, Leonardo

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Bone Marrow-Derived Progenitor Cells in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy von PESCINI, Francesca, CESARI, Francesca, GANDOLFO, Carlo, GORI, Anna M, ABBATE, Rosanna, PANTONI, Leonardo, INZITARI, Domenico, GIUSTI, Betti, SARTI, Cristina, ZICARI, Enza, BIANCHI, Silvia, DOTTI, Maria T, FEDERICO, Antonio, BALESTRINO, Maurizio, ENRICO, Adriano

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Relevance of brain lesion location for cognition in vascular mild cognitive impairment von Giorgio, Antonio, Di Donato, Ilaria, De Leucio, Alessandro, Zhang, Jian, Salvadori, Emilia, Poggesi, Anna, Diciotti, Stefano, Cosottini, Mirco, Ciulli, Stefano, Inzitari, Domenico, Pantoni, Leonardo, Mascalchi, Mario, Federico, Antonio, Dotti, Maria Teresa, De Stefano, Nicola

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Response to Letter by Mazzucco et al von Zicari, Enza, Tassi, Rossana, De Stefano, Nicola, Dotti, Maria Teresa

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Right-to-Left Shunt in CADASIL Patients : Prevalence and Correlation With Clinical and MRI Findings von ZICARI, Enza, TASSI, Rossana, STROMILLO, Maria L, PELLEGRINI, Michele, BIANCHI, Silvia, CEVENINI, Gabriele, GISTRI, Massimo, DE STEFANO, Nicola, FEDERICO, Antonio, DOTTI, Maria T

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Plasma Levels of Asymmetric Dimethylarginine in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarct and Leukoencephalopathy von Rufa, Alessandra, Blardi, Patrizia, De Lalla, Arianna, Cevenini, Gabriele, De Stefano, Nicola, Zicari, Enza, Auteri, Alberto, Federico, Antonio, Dotti, Maria Teresa

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A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss von Cardaioli, Elena, Da Pozzo, Paola, Gallus, Gian Nicola, Malandrini, Alessandro, Gambelli, Simona, Gaudiano, Carmen, Malfatti, Edoardo, Viscomi, Carlo, Zicari, Enza, Berti, Gianna, Serni, Giovanni, Dotti, Maria Teresa, Federico, Antonio

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Dysautonomic achalasia in two siblings with Sandhoff disease von Pellegrini, Michele, Zicari, Enza, Teresa Dotti, Maria, Federico, Antonio

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A novel heteroplasmic tRNASer(UCN) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss von Cardaioli, Elena, Da Pozzo, Paola, Gallus, Gian Nicola, Malandrini, Alessandro, Gambelli, Simona, Gaudiano, Carmen, Malfatti, Edoardo, Viscomi, Carlo, Zicari, Enza, Berti, Gianna, Serni, Giovanni, Dotti, Maria Teresa, Federico, Antonio

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Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1 von Gambelli, S, Malandrini, A, Berti, G, Gaudiano, C, Zicari, E, Brunori, P, Perticoni, G, Orrico, A, Galli, L, Sorrentino, V, Lunardi, J, Federico, A, Dotti, MT

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A novel heteroplasmic tRNA Ser(UCN) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss von Cardaioli, Elena, Da Pozzo, Paola, Gallus, Gian Nicola, Malandrini, Alessandro, Gambelli, Simona, Gaudiano, Carmen, Malfatti, Edoardo, Viscomi, Carlo, Zicari, Enza, Berti, Gianna, Serni, Giovanni, Dotti, Maria Teresa, Federico, Antonio

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