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Neuroscience Letters|March 21, 2007
Putative role of specific JAG1 gene exons in modulating clinical features in patients with leukoencephalopathyCarmine Ungaro, Teresa Sprovieri, Francesca L Conforti, et al.
Acta Neurologica Belgica|March 20, 2012
Phenotypic heterogeneity in hereditary motor neuropathy type V: a new case report seriesManuela Pennisi, Alberto Raggi, Rita Barone, et al.
Neuromolecular Medicine|May 14, 2014
Mutation analysis of MFN2, GJB1, MPZ and PMP22 in Italian patients with axonal Charcot-Marie-Tooth diseaseGiorgia Bergamin, Francesca Boaretto, Chiara Briani, et al.
Behavioural Brain Research|March 23, 2010
Morphological correlates of MAO A VNTR polymorphism: new evidence from cortical thickness measurementAntonio Cerasa, Andrea Cherubini, Aldo Quattrone, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
The gender effect in juvenile Huntington disease patients of Italian originMilena Cannella, Cinzia Gellera, Vittorio Maglione, et al.
Psychiatry Research|January 18, 2011
MAO A VNTR polymorphism and amygdala volume in healthy subjectsAntonio Cerasa, Aldo Quattrone, Maria C Gioia, et al.
Biological Psychiatry|October 6, 2005
Monoamine oxidase-a genetic variations influence brain activity associated with inhibitory control: new insight into the neural correlates of impulsivityLuca Passamonti, Francesco Fera, Angela Magariello, et al.
Acta Neurologica Belgica|October 15, 2018
ALS and CHARGE syndrome: a clinical and genetic studyCarmine Ungaro, Luigi Citrigno, Francesca Trojsi, et al.
Brain & Development|September 5, 2007
Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesisAlessandro Malandrini, Simona Gambelli, Maria Muglia, et al.
BMC Medical Genetics|March 15, 2019
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case reportTeresa Sprovieri, Carmine Ungaro, Serena Sivo, et al.
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