RINAUDO, Maria Teresa
RINAUDO, Maria Teresa
Dip. MEDICINA ED ONCOLOGIA SPERIMENTALE (attivo dal 01/01/1900 al 30/04/2013)
A defective L_MAG (large myelin-associated glycoprotein) is responsible for an adult-onset autosomal dominant orthochromatic leukodystrophy
2004-01-01 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
2009-01-01 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
2009-01-01 Prinetti A; Buccinnà B; Piccinini M; Scandroglio F; Prioni S; Valsecchi M; Lupino E; Ramondetti C; Sonnino S; Rinaudo MT
An approach to the timing of altered localization of TDP-43 in ALS motor neurons during disease progression
2009-01-01 Giordana MT; Grifoni S; Piccinini M; Pellerino A; De Marco G ; Buccinnà B ; Lupino E ; Naldi A; Magistrello M; Rinaudo MT
Dysfunctions in N_CAM and unexpected accumulation of PSA_NCAM in brain of Autosomal dominant adult onset leukodystrophy (ADLD)
2009-01-01 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
2007-01-01 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.
2011-01-01 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.
Modulation of glycolysis by high glucose in cultured human endothelial cells.
1994-01-01 BELTRAMO E.; LA SELVA M; PAGNOZZI F; PORTA M; CURTO M; PICCININI M; MIOLETTI S; RINAUDO MT; MOLINATTI G.M.
Modulation of glycolysis by high glucose in cultured human endothelial cells.
1995-01-01 BELTRAMO E; LA SELVA M; PAGNOZZI F; PORTA M; CURTO M; PICCININI M; MIOLETTI S; RINAUDO MT; MOLINATTI GM
Modulazione della glicolisi in cellule endoteliali umane sottoposte ad elevate concentrazioni di glucosio in vitro.
1994-01-01 BELTRAMO E.; LA SELVA M; PAGNOZZI F; CURTO M; PICCININI M; MIOLETTI S; PORTA M; RINAUDO M.T.; MOLINATTI G.M.
Modulazione della glicolisi in cellule endoteliali umane sottoposte ad elevate concentrazioni di glucosio in vitro.
1994-01-01 BELTRAMO E.; LA SELVA M; PAGNOZZI F; CURTO M; PICCININI M; MIOLETTI S; PORTA M; RINAUDO M.T.; MOLINATTI G.M.
Multidiscliplinary approach to cause and pathogenesis of an adult onset autosomal dominant orthochromatic leukodystrophy
2005-01-01 MT Giordana; L Palmucci; C D’Agostino; M Piccinini; A Brusco; MT Rinaudo
Myelin involvement in Niemann-Pick disease type A
2007-01-01 B Votta; M. Piccinini; S Grifoni; L Palmucci; A Heape; B Buccinnà; MT Rinaudo; MT Giordana
Myelin is involved in Niemann-Pick disease
2007-01-01 M T Giordana; S. Grifoni; B. Votta; A. Heape; B. Buccinnà; MT Rinaudo; M Piccinini
Myelin-associated glycoprotein is altered in a familial orthochromatic leukodystrophy
2004-01-01 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
2004-01-01 Giordana MT; Palmucci L; Piccinini M; Buccinnà B; Ramondetti C; Rinaudo MT
Myelin-associated glycoprotein is defective in a familial orthochromatic leukodystrophy
2004-01-01 Giordana MT; Palmucci L; Piccinini M; Ramondetti C; Rinaudo MT
Novel dysfunctions at the origin of hypomyelination, a feature of Niemann Pick type A
2011-01-01 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
2007-01-01 Buccinnà B; Piccinini M; Giordana MT; Ramondetti C; Lupino E; De Marco G; Votta B; Grifoni S; Rinaudo MT
TDP-43 redistribution is an early event in sporadic amyotrophic lateral sclerosis
2009-01-01 Giordana MT; Piccinini M; Grifoni S; De Marco G; Vercellino M; Magistrello M; Pellerino A; Buccinnà B; Lupino E; Rinaudo M T
| 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 | |
| An approach to the timing of altered localization of TDP-43 in ALS motor neurons during disease progression | 2009 | Giordana MT; Grifoni S; Piccinini M; Pellerino A; De Marco G ; Buccinnà B ; Lupino E ; Naldi A; Magistrello M; 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. | |
| Modulation of glycolysis by high glucose in cultured human endothelial cells. | 1994 | BELTRAMO E.; LA SELVA M; PAGNOZZI F; PORTA M; CURTO M; PICCININI M; MIOLETTI S; RINAUDO MT; MOLINATTI G.M. | |
| Modulation of glycolysis by high glucose in cultured human endothelial cells. | 1995 | BELTRAMO E; LA SELVA M; PAGNOZZI F; PORTA M; CURTO M; PICCININI M; MIOLETTI S; RINAUDO MT; MOLINATTI GM | |
| Modulazione della glicolisi in cellule endoteliali umane sottoposte ad elevate concentrazioni di glucosio in vitro. | 1994 | BELTRAMO E.; LA SELVA M; PAGNOZZI F; CURTO M; PICCININI M; MIOLETTI S; PORTA M; RINAUDO M.T.; MOLINATTI G.M. | |
| Modulazione della glicolisi in cellule endoteliali umane sottoposte ad elevate concentrazioni di glucosio in vitro. | 1994 | BELTRAMO E.; LA SELVA M; PAGNOZZI F; CURTO M; PICCININI M; MIOLETTI S; PORTA M; RINAUDO M.T.; MOLINATTI G.M. | |
| Multidiscliplinary approach to cause and pathogenesis of an adult onset autosomal dominant orthochromatic leukodystrophy | 2005 | MT Giordana; L Palmucci; C D’Agostino; M Piccinini; A Brusco; MT Rinaudo | |
| Myelin involvement in Niemann-Pick disease type A | 2007 | B Votta; M. Piccinini; S Grifoni; L Palmucci; A Heape; B Buccinnà; MT Rinaudo; MT Giordana | |
| Myelin is involved in Niemann-Pick disease | 2007 | M T Giordana; S. Grifoni; B. Votta; A. Heape; B. Buccinnà; MT Rinaudo; M Piccinini | |
| 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 | |
| TDP-43 redistribution is an early event in sporadic amyotrophic lateral sclerosis | 2009 | Giordana MT; Piccinini M; Grifoni S; De Marco G; Vercellino M; Magistrello M; Pellerino A; Buccinnà B; Lupino E; Rinaudo M T |