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Mostrati risultati da 21 a 40 di 46
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p14ARF/Mdm2/p53 pathway deregulation in two glioblastoma series: with and without differentiated areas 2002 Ghimenti, C.; Fiano, V.; Chiadò-piat, L.; Cavalla, P.; Schiffer, D.
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
TP53, CDKN2A/P16, CDKN2B/P14ARF, MDM2 interaction in glioblastomas 2001 D, Schiffer; C, Ghimenti; L, Chiadò-piat; V, Fiano
p14ARF, p16INK4a, MDM2 and TP53 changes compared with histological patterns in glioblastoma 2001 Ghimenti, C.; Chiadò-piat, L.; Fiano, V.; Lombard, E.; Schiffer, D.
CDKN2A/p16 in ependymomas. 2001 BORTOLOTTO S; CHIADÒ-PIAT L; CAVALLA P; BOSONE I; MAURO A; SCHIFFER D.
Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same family. 2000 L. PALMUCCI; MONGINI T; CHIADÒ-PIAT L; DORIGUZZI C; FUBINI A
CDKN2A/p16 inactivation in the prognosis of oligodendrogliomas. 2000 BORTOLOTTO S; CHIADÒ-PIAT L; CAVALLA P; BOSONE I; CHIÒ A; MAURO A; SCHIFFER D
Unusual clinical expression of dystrophinopathy in a female, mimicking a congenital myopathy. 1999 PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L ;UGO I
Variable histological expression of dystrophinopathy in two females. 1999 DORIGUZZI C ;PALMUCCI L ;MONGINI T ;CHIADÒ-PIAT L ;SAGGIORATO C ;UGO I ;HOFFMAN EP
Systematic use of dystrophin testing in muscle biopsies: results in 201 cases. 1997 DORIGUZZI C ;PALMUCCI L ;MONGINI T ;CHIADÒ-PIAT L ; MANISCALCO M ;RESTAGNO G
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease. 1997 MIGHELI A ;MONGINI T ;DORIGUZZI C ;CHIADÒ-PIAT L ;PIVA R ;UGO I ;PALMUCCI L
Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical study. 1996 SCHIFFER D ;CAVALLA P ;MIGHELI A ;GIORDANA MT ;CHIADÒ-PIAT L
Quantitative and qualitative alterations of dystrophin are expressed in muscle cell cultures of Xp21 muscular dystrophy patients (Duchenne and Becker type). 1996 MONGINI T; DORIGUZZI C; PALMUCCI L; CHIADÒ-PIAT L
Metachromatic dye-Ca++ATPase method in pathological muscle: a study of 382 muscle biopsies. 1994 DORIGUZZI C ;PALMUCCI L ;MONGINI T ;MANISCALCO M ;CHIADÒ-PIAT L ;DE ANGELIS MS
Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60-year-old man with 26 percent deletion of the dystrophin gene. 1994 PALMUCCI L; DORIGUZZI C; MONGINI T; RESTAGNO G; CHIADÒ-PIAT L; MANISCALCO M
Adult onset nemaline myopathy: a distinct nosologic entity? 1993 PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L
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
Clinical spectrum of McArdle disease: three cases with unusual expression. 1993 CHIADÒ-PIAT L ;MONGINI T ;DORIGUZZI C ;MANISCALCO M ;PALMUCCI L
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
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
Mostrati risultati da 21 a 40 di 46
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