Sfoglia per Autore

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Titolo Data di pubblicazione Autore(i) File
Proteins phosphorylated on tyrosine as markers of human tumor cell lines 1987 Giordano S; Di Renzo MF; Cirillo D; Naldini L; Chiado' Piat L; Comoglio PM
p145, a protein with associated tyrosine kinase activity in a human gastric carcinoma cell line. 1988 S. GIORDANO; M. DI RENZO; R. FERRACINI; L. CHIADÒ-PIAT; P.M. COMOGLIO
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
Proteins phosphorylated on tyrosine as markers of human tumor cell lines 1988 S. Giordano; M.F. Di Renzo; D. Cirillo; L. Naldini; L. Chiadò Piat; P.M. Comoglio
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
Myoglobinuria and carnitine palmityl transferase deficiency in father and son. 1991 MONGINI T; DORIGUZZI C; L. PALMUCCI; CHIADÒ-PIAT L; MANISCALCO M; SCHIFFER D
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
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
Adult onset nemaline myopathy: a distinct nosologic entity? 1993 PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L
Clinical spectrum of McArdle disease: three cases with unusual expression. 1993 CHIADÒ-PIAT L ;MONGINI T ;DORIGUZZI C ;MANISCALCO M ;PALMUCCI 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
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
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
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
Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical study. 1996 SCHIFFER D ;CAVALLA P ;MIGHELI A ;GIORDANA MT ;CHIADÒ-PIAT L
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
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
CDKN2A/p16 inactivation in the prognosis of oligodendrogliomas. 2000 BORTOLOTTO S; CHIADÒ-PIAT L; CAVALLA P; BOSONE I; CHIÒ A; MAURO A; SCHIFFER D
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