Sfoglia per Autore
Complex IV change in the mitochondria respiratory chain of chronic external ophtalmoplegia : a review of our cases
1985 N. Bresolin, M. Moggio, L. Bet, G. Meola, A. Bordoni, G. Pellegrini, E. Nobile-Orazio, G. Scarlato
5 ' azacytidine enhances exogenous gene expression in skeletal muscle
1999 M. D'Angelo, C. Ausenda, Y. Torrente, A. Bordoni, S. Corti, R. Del Bo, M. Perini, M. Colucci, G. Comi, N. Bresolin, G. Scarlato
Neuronal differentiation of murine bone marrow Thy-1- and Sca-1-positive cells
2003 F. Locatelli, S.P. Corti, C. Donadoni, M. Guglieri, F. Capra, S. Strazzer, S. Salani, R. Del Bo, F.R. Fortunato, A. Bordoni, G.P. Comi
Survival motor neuron (SMN1 and SMN2) genes copy number in multifocal motor neuropathy
2005 F. Saladino, M. Scarlato, M. Carpo, A. Bordoni, E. Nobile-Orazio, N. Bresolin, G.P. Comi
ALDH positive neural stem cells generate motor neurons and promote functional recovery in NMD mice, an animal model of SMARD1
2005 F. Locatelli, S. Corti, D. Papadimitriou, C. Donadoni, M. Crimi, R. Del Bo, A. Bordoni, S. Strazzer, S. Salani, N. Bresolin, G.P. Comi
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy
2005 M. Sciacco, A. Prelle, G. Fagiolari, A. Bordoni, M.Crimi, A. Di Fonzo, P. Ciscato, C. Lamperti, E. D'Adda, S. Jann, N. Bresolin, G.P. Comi, M. Moggio
Mutations in the mitochondrial DNA control region in mitochondrial disorders associated with defects in mtDNA maintenance and aging. “Frontiers in DNA Research
2005 R. Del Bo, S. Ghezzi, A. Bordoni, M. Crimi, M. Sciacco, N. Bresolin, G.P. Comi
Skeletal muscle gene expression profiling in mitochondrial disorders
2005 M. Crimi, A. Bordoni, G. Menozzi, L. Riva, F. Fortunato, S. Galbiati, R. Del Bo, U. Pozzoli, N. Bresolin, G.P. Comi
Autosomal dominant and recessive limb-girdle muscular dystrophies: relative frequency in a large Italian population
2005 M. Guglieri, F. Magri, R. Cagliani, M.G. D'Angelo, A. Prelle, F. Fortunato, S. Lucchiari, S. Salani, R. Del Bo, A. Bordoni, S. Ghezzi, C. Zecca, C. Lamperti, M. Moggio, N. Bresolin, G.P. Comi
Fatal R631C mutation is also present in the adult form of CPTII deficiency
2005 O. Musumeci, A. Bordoni, M. Aguennouz, C. Rodolico, M. Autunno, V. Cianci, G. Vita, F. Taroni, G.P. Comi, A. Toscano
ALDH neural stem cells generate motor neurons and ameliorate the phenotype of nmd mice, an animal model of SMARD1
2005 F. Locatelli, S. Corti, D. Papadimitriou, C. Donadoni, M. Crimi, R. Del Bo, A. Bordoni, S. Strazzer, S. Salani, N. Bresolin, G.P. Comi
Transplantation of ALDH expressing neuronal stem cell subpopulation derived from spinal cord into Nmd mice, an animal model of SMARD1
2005 S.P. Corti, F. Locatelli, D. Papadimitriou, C. Donadoni, M. Crimi, R. DEL BO, A. Bordoni, S. Strazzer, S. Salani, N. Bresolin, G.P. Comi
The limb girdle muscular dystrophies: clinical, biochemical and genetic evaluation of a large Italian population
2005 M. Guglieri, F. Magri, M.G. D'Angelo, R. Cagliani, A. Bordoni, D. Ronchi, S. Grezzi, R. Del Bo, A. Prelle, M. Moggio, T. Mongini, M. Mora, A.C. Turconi, N. Bresolin, G.P. Comi
Bank of DNA, cell lines and nerve-muscle-cardiac tissues
2005 M. Sciacco, A. Prelle, G. Fagiolari, P. Ciscato, M. Serafini, S. Livraghi, L. Napoli, C. Lamperti, E. D'Adda, C. Zecca, M.E. Fruguglietti, V. Lucchini, G.P. Comi, A. Bordoni, F. Fortunato, Y. Torrente, S. Galbiati
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of Andersen disease associated with a new mutation in GBE gene
2006 C. Lamperti, S. Salani, S. Lucchiari, A. Bordoni, M.E. Fruguglietti, V. Crugnola, A. Cappellini, A. Prelle, N. Bresolin, G.P. Comi, M. Moggio
A region in the dystrophin gene major hot-spot harbors a cluster of deletion breakpoints and generates double-strand breaks in yeast
2006 M. Sironi, U. Pozzoli, G.P. Comi, S. Riva, A. Bordoni, N. Bresolin, D.K. Nag
Screening of Twinkle gene in POLG1- and ANT1-negative patients with mitochondrial myopathy and multiple mitochondrial DNA deletions : four new mutations
2006 R. Virgilio, D. Ronchi, A. Bordoni, L. Adobbati, G.M. Hadjigeorgiou, D. Kafetsouli, E. Tsironi, A. Papadimitriou, M. Moggio, N. Bresolin, G.P. Comi
New twinkle gene mutations in PEO patients with multiple mitochondrial DNA deletions
2006 R. Virgilio, A. Bordoni, D. Ronchi, G.M. Hadjigeorgiou, R. Del Bo, V. Crugnola, D. Kafetsouli, E. Tsironi, A. Papadimitriou, N. Bresolin, G.P. Comi
Screening of mitochondrial myopathy with mtDNA multiple deletions and characterization of patients without mutations in known loci
2006 R. Virgilio, D. Ronchi, A. Bordoni, L. Adobbati, G.M. Hadjigeorgiou, F. Saladino, A. Papadimitriou, M. Moggio, N. Bresolin, G.P. Comi
A yeast system to study double strand break formation in the DMD deletion prone region and in human recombination hotspots
2006 R. Cagliani, U. Pozzoli, R. Riva, G.P. Comi, D.K. Nag, N. Bresolin, A. Bordoni, M. Sironi
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