CRIMI, MARCO
CRIMI, MARCO
DIPARTIMENTO DI SCIENZE NEUROLOGICHE (attivo dal 01/01/2001 al 27/04/2012)
Genetic variation in the interleukin-28B gene is not associated with fibrosis progression in patients with chronic hepatitis C and known date of infection
2011 F. Marabita, A.M. Aghemo, S. De Nicola, M. Rumi, C. Cheroni, R. Scavelli, M. Crimi, R.M. Soffredini, S. Abrignani, R. De Francesco, M. Colombo
New mutations in TK2 gene associated with mitochondrial DNA depletion
2006 S. Galbiati, A. Bordoni, D. Papadimitriou, A. Toscano, C. Rodolico, E. Katsarou, M. Sciacco, A. Garufi, A. Prelle, M. Aguennouz, M. Bonsignore, M. Crimi, A. Martinuzzi, N. Bresolin, A. Papadimitriou, G.P. Comi
Transplanted ALDH(hi)SSC(lo) neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1
2006 S.P. Corti, F. Locatelli, D. Papadimitriou, C. Donadoni, R. DEL BO, M. Crimi, A. Bordoni, F.R. Fortunato, S. Strazzer, G. Menozzi, S. Salani, N. Bresolin, G.P. Comi
Mutations in the mitochondrial DNA control region in mitochondrial disorders associated with defects in mtDNA maintenance and aging
2006 R. Del Bo, S. Ghezzi, A. Bordoni, M. Crimi, M. Sciacco, N. Bresolin, G.P. Comi
Association between VEGF gene and sporadic Alzheimer's disease.
2005 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli-Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, M. Crimi, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
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
Association between VEGF gene and sporadic Alzheimer’s Disease
2005 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, M. Crimi, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
Vascular endothelial growth factor gene variability is associated with increased risk for AD
2005 R. Del Bo, M. Scarlato, S. Ghezzi, F.M. Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, M. Crimi, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi, M. Crimi, C. Fenoglio
Molecular research technologies in mitochondrial diseases: the microarray approach
2005 M. Crimi ,S.F.O'Hearn ,D.C. Wallace ,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
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
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
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion
2003 M. Crimi, R. Del Bo, S. Galbiati, M. Sciacco, A. Bordoni, N. Bresolin, G. Comi