CHIADO'-PIAT, Loredana
CHIADO'-PIAT, Loredana
NEUROSCIENZE "RITA LEVI MONTALCINI"
A case of to treatment with piridostigmine bromide: a new phenotype?
2011-01-01 L. Vercelli; S. Benedetti; E. Vittonatto ; L. Chiadò-Piat; E. Pilati; T. Mongini.
A young boy with a new mutation in lamin A/C gene responsive to treatment with ACHE inhibitors
2011-01-01 Vercelli, L; Benedetti, S; Vittonatto, E; Chiado'-Piat, L; Pilati, E; Pinessi, L; Mongini, T
Adult onset nemaline myopathy: a distinct nosologic entity?
1993-01-01 PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria.
2002-01-01 MONGINI T; DORIGUZZI C; BOSONE I; CHIADÒ-PIAT L; HOFFMAN EP; L. PALMUCCI
Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical study.
1996-01-01 SCHIFFER D ;CAVALLA P ;MIGHELI A ;GIORDANA MT ;CHIADÒ-PIAT L
CDKN2A/p16 in ependymomas.
2001-01-01 BORTOLOTTO S; CHIADÒ-PIAT L; CAVALLA P; BOSONE I; MAURO A; SCHIFFER D.
CDKN2A/p16 inactivation in the prognosis of oligodendrogliomas.
2000-01-01 BORTOLOTTO S; CHIADÒ-PIAT L; CAVALLA P; BOSONE I; CHIÒ A; MAURO A; SCHIFFER D
Clinical spectrum of McArdle disease: three cases with unusual expression.
1993-01-01 CHIADÒ-PIAT L ;MONGINI T ;DORIGUZZI C ;MANISCALCO M ;PALMUCCI L
Clinicopathological features and disease course in three patients with focal myositis
2015-01-01 Bortolani, S.; Vercelli, L.; Ponzalino, V.; Boschi, S.; Vittonatto, E.; Chiadò-Piat, L.; Mongini, T.
Complete recovery in a severe case of anti-ssa positive necrotizing myopathy after rituximab therapy
2012-01-01 Giobbe, Ml; Vercelli, L; Vittonatto, E; Chiadò-Piat, L; Roccatello, D; Pinessi, L; Mongini, T
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalis.
1993-01-01 DORIGUZZI C ;PALMUCCI L ;MONGINI T ;BERTOLOTTO A ;MANISCALCO M ;CHIADÒ-PIAT L ;ZINA AM ;BUNDINO S
Deregulated tyrosine kinases detected in human tumors by means of antibodies against phosphotyrosine
1989-01-01 M.F. Di Renzo; S. Giordano; L. Chiadò Piat; R.P. Narsimhan; P.M. Comoglio
Deregulation of the p14ARF/Mdm2/p53 pathway and G1/S transition in two glioblastoma sets.
2003-01-01 GHIMENTI C ;FIANO V ;CHIADÒ-PIAT L ;CHIÒ A ;CAVALLA P ;SCHIFFER D
Differential diagnosis of vacuolar muscle biopsies: use of p62, LC3 and LAMP2 immunohistochemistry
2017-01-01 Vittonatto, Elisa; Boschi, Silvia; CHIADò-Piat, Loredana; Ponzalino, Valentina; Bortolani, Sara; Brusa, Chiara; Rainero, Innocenzo; Ricci, Federica; Vercelli, Liliana; Mongini, Tiziana
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy.
1992-01-01 PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L ;RESTAGNO G ;CARBONARA A ;PAOLILLO V
Distribution of activated caspase-3 in relation with apoptosis in human malignant gliomas.
2001-01-01 D. SCHIFFER; FIANO V; CHIADÒ-PIAT L; MORTARA P; RICHIARDI P; CAVALLA P
Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same family.
2000-01-01 L. PALMUCCI; MONGINI T; CHIADÒ-PIAT L; DORIGUZZI C; FUBINI A
Evidence for autocrine activation of a tyrosine kinase in a human gastric carcinoma cell line.
1988-01-01 GIORDANO S ;DI RENZO MF ;NARSIMHAN RP ;TAMAGNONE L ;GERBAUDO EV ;CHIADÓ-PIAT L ;COMOGLIO PM
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy.
1993-01-01 DORIGUZZI C ;PALMUCCI L ;MONGINI T ;CHIADÒ-PIAT L ;RESTAGNO G ;FERRONE M
Glycogen storage disease type II diagnosed in a 74-year-old woman
2004-01-01 BOSONE I; VERCELLI L; MONGINI T; CHIADÓ-PIAT L; VITTONATTO E; PALMUCCI L; SERVIDEI S; SILVESTRI G
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A case of to treatment with piridostigmine bromide: a new phenotype? | 2011 | L. Vercelli; S. Benedetti; E. Vittonatto ; L. Chiadò-Piat; E. Pilati; T. Mongini. | |
A young boy with a new mutation in lamin A/C gene responsive to treatment with ACHE inhibitors | 2011 | Vercelli, L; Benedetti, S; Vittonatto, E; Chiado'-Piat, L; Pilati, E; Pinessi, L; Mongini, T | |
Adult onset nemaline myopathy: a distinct nosologic entity? | 1993 | PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L | |
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria. | 2002 | MONGINI T; DORIGUZZI C; BOSONE I; CHIADÒ-PIAT L; HOFFMAN EP; L. PALMUCCI | |
Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical study. | 1996 | SCHIFFER D ;CAVALLA P ;MIGHELI A ;GIORDANA MT ;CHIADÒ-PIAT L | |
CDKN2A/p16 in ependymomas. | 2001 | BORTOLOTTO S; CHIADÒ-PIAT L; CAVALLA P; BOSONE I; MAURO A; SCHIFFER D. | |
CDKN2A/p16 inactivation in the prognosis of oligodendrogliomas. | 2000 | BORTOLOTTO S; CHIADÒ-PIAT L; CAVALLA P; BOSONE I; CHIÒ A; MAURO A; SCHIFFER D | |
Clinical spectrum of McArdle disease: three cases with unusual expression. | 1993 | CHIADÒ-PIAT L ;MONGINI T ;DORIGUZZI C ;MANISCALCO M ;PALMUCCI L | |
Clinicopathological features and disease course in three patients with focal myositis | 2015 | Bortolani, S.; Vercelli, L.; Ponzalino, V.; Boschi, S.; Vittonatto, E.; Chiadò-Piat, L.; Mongini, T. | |
Complete recovery in a severe case of anti-ssa positive necrotizing myopathy after rituximab therapy | 2012 | Giobbe, Ml; Vercelli, L; Vittonatto, E; Chiadò-Piat, L; Roccatello, D; Pinessi, L; Mongini, T | |
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalis. | 1993 | DORIGUZZI C ;PALMUCCI L ;MONGINI T ;BERTOLOTTO A ;MANISCALCO M ;CHIADÒ-PIAT L ;ZINA AM ;BUNDINO S | |
Deregulated tyrosine kinases detected in human tumors by means of antibodies against phosphotyrosine | 1989 | M.F. Di Renzo; S. Giordano; L. Chiadò Piat; R.P. Narsimhan; P.M. Comoglio | |
Deregulation of the p14ARF/Mdm2/p53 pathway and G1/S transition in two glioblastoma sets. | 2003 | GHIMENTI C ;FIANO V ;CHIADÒ-PIAT L ;CHIÒ A ;CAVALLA P ;SCHIFFER D | |
Differential diagnosis of vacuolar muscle biopsies: use of p62, LC3 and LAMP2 immunohistochemistry | 2017 | Vittonatto, Elisa; Boschi, Silvia; CHIADò-Piat, Loredana; Ponzalino, Valentina; Bortolani, Sara; Brusa, Chiara; Rainero, Innocenzo; Ricci, Federica; Vercelli, Liliana; Mongini, Tiziana | |
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy. | 1992 | PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L ;RESTAGNO G ;CARBONARA A ;PAOLILLO V | |
Distribution of activated caspase-3 in relation with apoptosis in human malignant gliomas. | 2001 | D. SCHIFFER; FIANO V; CHIADÒ-PIAT L; MORTARA P; RICHIARDI P; CAVALLA P | |
Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same family. | 2000 | L. PALMUCCI; MONGINI T; CHIADÒ-PIAT L; DORIGUZZI C; FUBINI A | |
Evidence for autocrine activation of a tyrosine kinase in a human gastric carcinoma cell line. | 1988 | GIORDANO S ;DI RENZO MF ;NARSIMHAN RP ;TAMAGNONE L ;GERBAUDO EV ;CHIADÓ-PIAT L ;COMOGLIO PM | |
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy. | 1993 | DORIGUZZI C ;PALMUCCI L ;MONGINI T ;CHIADÒ-PIAT L ;RESTAGNO G ;FERRONE M | |
Glycogen storage disease type II diagnosed in a 74-year-old woman | 2004 | BOSONE I; VERCELLI L; MONGINI T; CHIADÓ-PIAT L; VITTONATTO E; PALMUCCI L; SERVIDEI S; SILVESTRI G |