Giuseppe De Michele

发表

Brain white matter damage in SCA1 and SCA2. An in vivo study using voxel-based morphometry, histogram analysis of mean diffusivity and tract-based spatial statistics

Mario Mascalchi, Elena Salvatore, Carlo Tessa, 2008, NeuroImage.

Coupling Energy and Daylighting Simulation for Complex Fenestration Systems

Ulrich Filippi Oberegger, Giuseppe De Michele, L. Baglivo, 2014 .

Opportunities and challenges for performance prediction of dynamic complex fenestration systems (CFS)

Fabio Favoino, Andrea Gasparella, R.C.G.M. Loonen, 2018 .

Optimised Parametric Model of a Modular Multifunctional Climate Adaptive Facade for Shopping Centers Retrofitting

Annamaria Belleri, Riccardo Pinotti, Stefano Avesani, 2017 .

Brain white matter tracts degeneration in Friedreich ataxia. An in vivo MRI study using tract-based spatial statistics and voxel-based morphometry

Mario Mascalchi, Fabrizio Salvi, Ilaria Bartolomei, 2008, NeuroImage.

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.

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. 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.

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.

The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease

Nicholas W. Wood, Matthew J. Farrer, Vincenzo Bonifati, 1999, Neuroscience Letters.