Alessandro Filla

发表

A multilayer perceptron neural network-based approach for the identification of responsiveness to interferon therapy in multiple sclerosis patients

Antonino Staiano, Giuseppe Longo, Elena Salvatore, 2010, Inf. Sci..

DNA damage induced by polyglutamine-expanded proteins.

Alessandro Filla, G. De Michele, A. Filla, 2003, Human molecular genetics.

Supratentorial and infratentorial damage in spinocerebellar ataxia 2: A diffusion‐weighted MRI study

Elena Salvatore, Arturo Brunetti, Marco Salvatore, 2014, Movement disorders : official journal of the Movement Disorder Society.

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data

Alexandra Durr, Marcella Masciullo, Dagmar Timmann, 2013, The Lancet Neurology.

Multiple sclerosis and hepatitis C virus infection are associated with single nucleotide polymorphisms in interferon pathway genes.

Elena Salvatore, Lucia Sacchetti, Francesco Borrelli, 2008, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings

Paola Giunti, Till-Karsten Hauser, Dagmar Timmann, 2011, The Cerebellum.

Identification by [ 99 mTc ] ECD SPECT of anterior cingulate hypoperfusion in progressive supranuclear palsy , in comparison with Parkinson ’ s disease

Elena Salvatore, Marco Salvatore, Andrea Varrone, 2007 .

Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease

Sergio Cocozza, Bertrand Fontaine, Giuseppe De Michele, 1998, Cell.

A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study

Mariano Serrao, Francesco Pierelli, Giuseppe Arcuria, 2017, Neurological Sciences.

Self‐rated health status in spinocerebellar ataxia—Results from a European multicenter study

Paola Giunti, Dagmar Timmann, Sylvia Boesch, 2010, Movement disorders : official journal of the Movement Disorder Society.

Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation.

Charles Duyckaerts, Giorgio Casari, Pio D'Adamo, 2004, Archives of neurology.

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes

Sergio Cocozza, Giuseppe De Michele, Lucio Santoro, 1996, Journal of the Neurological Sciences.

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

Paola Giunti, Alexandra Durr, Robyn Labrum, 2015, The Lancet Neurology.

Comparison between a dual-head and a brain-dedicated SPECT system in the measurement of the loss of dopamine transporters with [123I]FP-CIT

Elena Salvatore, Marco Salvatore, Andrea Varrone, 2008, European Journal of Nuclear Medicine and Molecular Imaging.

Identification by [99mTc]ECD SPECT of anterior cingulate hypoperfusion in progressive supranuclear palsy, in comparison with Parkinson’s disease

Elena Salvatore, Marco Salvatore, Andrea Varrone, 2007, European Journal of Nuclear Medicine and Molecular Imaging.

Modifications of resting state networks in spinocerebellar ataxia type 2

Mario Quarantelli, Arturo Brunetti, Sirio Cocozza, 2015, Movement disorders : official journal of the Movement Disorder Society.

Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2.

Giovanni Coppola, Fuying Gao, Genevieve Konopka, 2014, Human molecular genetics.