Sfoglia per Autore
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases
2001 A. Brega, J. Narula, E. Arbustini
The mitochondrial DNA mutation T12297C affects a highly conserved nucleotide of tRNA(Leu(CUN)) and is associated with dilated cardiomyopathy
2001 M. Grasso, M. Diegoli, A. Brega, C. Campana, L. Tavazzi, E. Arbustini
A novel mtDNA point mutation in tRNA(Val) is associated with hypertrophic cardiomyopathy and MELAS
2004 F. Menotti, A. Brega, M. Diegoli, M. Grasso, M.G. Modena, E. Arbustini
Identification of sixty-two novel and twelve known FBN1 mutations in eighty-one unrelated probands with Marfan syndrome and other fibrillinopathies
2005 E. Arbustini, M. Grasso, S. Ansaldi, C. Malattia, A. Pilotto, E. Porcu, E. Disabella, N. Marziliano, A. Pisani, L. Lanzarini, S. Mannarino, D. Larizza, M. Mosconi, E. Antoniazzi, M.C. Zoia, G. Meloni, L. Magrassi, A. Brega, M.F. Bedeschi, I. Torrente, F. Mari, L. Tavazzi
Early diagnosis of Wilson Disease in a six-year-old child
2006 A.G.Lo Curto, A. Marchi, M. Grasso, E. Arbustini, G. Loudianos, A.Brega
Brain pseudoatrophy and mental regression on valproate and a mitochondrial DNA mutation
2006 C.A. Galimberti, M. Diegoli, I. Sartori, C. Uggetti, A. Brega, A. Tartara, E. Arbustini
Gene symbol : LMNA
2007 E. Arbustini, M. Pasotti, A. Pilotto, M. Diegoli, A. Brega, E. Disabella, M. Grasso, N. Marziliano
Barth syndrome associated with compound hemizygosity and heterozygosity of the TAZ and LDB3 genes
2007 N. Marziliano, S. Mannarino, L. Nespoli, M. Diegoli, M. Pasotti, C. Malattia, M. Grasso, A. Pilotto, E. Porcu, A. Raisaro, C. Raineri, R. Dore, P.P. Maggio, A. Brega, E. Arbustini
Ultrastructural definition of apoptosis in heart failure
2008 E. Arbustini, A. Brega, J. Narula
The shortness of Pygmies is associated with severe under-expression of the growth hormone receptor
2009 M. Bozzola, P. Travaglino, N. Marziliano, C. Meazza, S. Pagani, M. Grasso, M. Tauber, M. Diegoli, A. Pilotto, E. Disabella, P. Tarantino, A. Brega, E. Arbustini
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