Sfoglia per Autore
Proteins phosphorylated on tyrosine as markers of human tumor cell lines
1987-01-01 Giordano S; Di Renzo MF; Cirillo D; Naldini L; Chiado' Piat L; Comoglio PM
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
Proteins phosphorylated on tyrosine as markers of human tumor cell lines
1988-01-01 S. Giordano; M.F. Di Renzo; D. Cirillo; L. Naldini; L. Chiadò Piat; P.M. Comoglio
p145, a protein with associated tyrosine kinase activity in a human gastric carcinoma cell line.
1988-01-01 S. GIORDANO; M. DI RENZO; R. FERRACINI; L. CHIADÒ-PIAT; P.M. COMOGLIO
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
Myoglobinuria and carnitine palmityl transferase deficiency in father and son.
1991-01-01 MONGINI T; DORIGUZZI C; L. PALMUCCI; CHIADÒ-PIAT L; MANISCALCO M; SCHIFFER D
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy.
1992-01-01 PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L ;RESTAGNO G ;CARBONARA A ;PAOLILLO V
Adult onset nemaline myopathy: a distinct nosologic entity?
1993-01-01 PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L
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
Clinical spectrum of McArdle disease: three cases with unusual expression.
1993-01-01 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.
1993-01-01 DORIGUZZI C ;PALMUCCI L ;MONGINI T ;CHIADÒ-PIAT L ;RESTAGNO G ;FERRONE M
Metachromatic dye-Ca++ATPase method in pathological muscle: a study of 382 muscle biopsies.
1994-01-01 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.
1994-01-01 PALMUCCI L; DORIGUZZI C; MONGINI T; RESTAGNO G; CHIADÒ-PIAT L; MANISCALCO M
Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical study.
1996-01-01 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).
1996-01-01 MONGINI T; DORIGUZZI C; PALMUCCI L; CHIADÒ-PIAT L
Systematic use of dystrophin testing in muscle biopsies: results in 201 cases.
1997-01-01 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.
1997-01-01 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.
1999-01-01 PALMUCCI L ;DORIGUZZI C ;MONGINI T ;CHIADÒ-PIAT L ;UGO I
Variable histological expression of dystrophinopathy in two females.
1999-01-01 DORIGUZZI C ;PALMUCCI L ;MONGINI T ;CHIADÒ-PIAT L ;SAGGIORATO C ;UGO I ;HOFFMAN EP
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
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