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BMC Medical Genetics|April 3, 2014
Novel SPAST deletion and reduced DPY30 expression in a Spastic Paraplegia type 4 kindredLoretta Racis, Eugenia Storti, Maura Pugliatti, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 23, 2013
Infantile-onset ascending hereditary spastic paralysis: a case report and brief literature reviewLoretta Racis, Alessandra Tessa, Maura Pugliatti, et al.
Journal of Neurology|February 13, 2014
Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1Roberto Di Fabio, Christian Marcotulli, Alessandra Tessa, et al.
Journal of Neurology|October 22, 2013
The high prevalence of hereditary spastic paraplegia in Sardinia, insular ItalyLoretta Racis, Alessandra Tessa, Roberto Di Fabio, et al.
Journal of Neurology|May 11, 2015
Acute optic neuropathy associated with a novel MFN2 mutationLuca Leonardi, Christian Marcotulli, Eugenia Storti, et al.
Muscle & Nerve|September 27, 2014
Muscle fiber type disproportion (FTD) in a family with mutations in the LMNA geneLucia Ruggiero, Chiara Fiorillo, Alessandra Tessa, et al.
Diabetes & Vascular Disease Research|June 10, 2011
Circulating endothelial progenitor cells in women with gestational alterations of glucose toleranceGiuseppe Penno, Laura Pucci, Daniela Lucchesi, et al.
Journal of Neurology|February 26, 2016
Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/CYP2U1 familyLuca Leonardi, Lucia Ziccardi, Christian Marcotulli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 10, 2013
Cerebellum and neuropsychiatric disorders: insights from ARSACSAndrea Mignarri, Alessandra Tessa, Maria Alessandra Carluccio, et al.
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