RAMONDETTI, Cristina

RAMONDETTI, Cristina  

ONCOLOGIA  

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Risultati 1 - 13 di 13 (tempo di esecuzione: 0.012 secondi).
Titolo Data di pubblicazione Autore(i) File
A defective L_MAG (large myelin-associated glycoprotein) is responsible for an adult-onset autosomal dominant orthochromatic leukodystrophy 2004 Giordana MT; Palmucci L; Piccinini M; Buccinnà B; Ramondetti C; Rinaudo MT
Alterations of protein and lipid patterns in brain white matter of ASMKO mice, the animal model of Niemann-Pick disease type A 2009 Piccinini M; Buccinnà B; Prinetti A; Scandroglio F; Prioni S; Valsecchi M; Lupino E; Ramondetti C; Sonnino S; Rinaudo MT
Altered sphingolipid metabolism in acidic sphingomyelinase knocout mice, an animal model for Niemann-Pick disease type A 2009 Prinetti A; Buccinnà B; Piccinini M; Scandroglio F; Prioni S; Valsecchi M; Lupino E; Ramondetti C; Sonnino S; Rinaudo MT
Dysfunctions in N_CAM and unexpected accumulation of PSA_NCAM in brain of Autosomal dominant adult onset leukodystrophy (ADLD) 2009 Buccinnà B; De Marco G; Piccinini M; Lupino E; Lomartire A; Ramondetti C; Grifoni S; Giordana MT; Rinaudo MT
Expression pattern of the 20S proteasome subunits following T cell activation 2007 Lupino E; Piccinini M; Buccinnà B; Ramondetti C; De Marco G; Rinaudo MT
Increased cytoplasmic mislocalization of TAR DNA binding protein 43 (TDP-43) in circulating lymphomonocytes of ALS patients recapitulates the major dysfunction featuring motor neurons in the disease. 2011 De Marco G; Lupino E; Grifoni S; Calvo A; Moglia C; Buccinnà B; Ramondetti C; Lomartire A; Piccinini M; Rinaudo MT;Giordana MT; Chiò A.
Myelin-associated glycoprotein is altered in a familial orthochromatic leukodystrophy 2004 Giordana MT; Palmucci L; Leombruni S; Vaula G; D'Agostino C; Piccinini M; Buccinnà B; Ramondetti C; Rinaudo MT
Myelin-associated glycoprotein is defective in a familail orthochromatic leukodystrophy 2004 Giordana MT; Palmucci L; Piccinini M; Buccinnà B; Ramondetti C; Rinaudo MT
Myelin-associated glycoprotein is defective in a familial orthochromatic leukodystrophy 2004 Giordana MT; Palmucci L; Piccinini M; Ramondetti C; Rinaudo MT
Novel dysfunctions at the origin of hypomyelination, a feature of Niemann Pick type A 2011 Buccinnà B; Lomartire A; Ramondetti C; De Marco G; Rinaudo MT; Lupino E; Piccinini M
Reduced expression of proteins characterizing myelin sheaths in brain of acid sphingomyelinase-deficinet mice, the animal model of Niemann-Pick disease type A 2007 Buccinnà B; Piccinini M; Giordana MT; Ramondetti C; Lupino E; De Marco G; Votta B; Grifoni S; Rinaudo MT
The expression pattern of TAR DNA-binding protein 43 (TDP-43) in peripheral blood mononuclear cells (PBMC) in individuals affected by amyotrophific lateral sclerosis (ALS) and their healthy relatives 2009 De Marco G; Piccinini M; Lupino E; Lomartire A; Buccinnà B; Ramondetti C; Grifoni S; Giordana MT; Rinaudo MT
The molecular basis of the hypomyelination characterizing the brains of sphingomyelinase-deficient mice, an animal model of Niemann-Pick disease type A 2009 Buccinnà B; Piccinini M; Prinetti A; Scandroglio F; Prioni S; Valsecchi M; Lupino E; Ramondetti C; De Marco G; Lomartire A; Giordana M T; Sonnino S; Rinaudo M T