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au.\*:("CANCIANI, Maria Teresa")

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Plasma levels of the von Willebrand factor-cleaving protease in physiological and pathological conditions in childrenKAVAKLI, Kaan; CANCIANI, Maria Teresa; MANNUCCIO MANNUCCI, Pier et al.Pediatric hematology and oncology. 2002, Vol 19, Num 7, pp 467-473, issn 0888-0018Article

Plasma levels of von Willebrand factor regulate ADAMTS-13, its major cleaving proteaseMANNUCCI, Pier Mannuccio; CAPOFERRI, Cristina; CANCIANI, Maria Teresa et al.British journal of haematology. 2004, Vol 126, Num 2, pp 213-218, issn 0007-1048, 6 p.Article

Patients with localized and disseminated tumors have reduced but measurable levels of ADAMTS-13 (von Willebrand factor cleaving protease)MANNUCCIO MANNUCCI, Pier; KARIMI, Mehran; MOSALAEI, Ahmad et al.Haematologica (Roma). 2003, Vol 88, Num 4, pp 454-458, issn 0390-6078, 5 p.Article

von Willebrand factor cleaving protease (ADAMTS-13) and ADAMTS-13 neutralizing autoantibodies in 100 patients with thrombotic thrombocytopenic purpuraPEYVANDI, Flora; FERRARI, Silvia; LAVORETANO, Silvia et al.British journal of haematology. 2004, Vol 127, Num 4, pp 433-439, issn 0007-1048, 7 p.Article

Von Willebrand factor cleaving protease (ADAMTS-13) in 123 patients with connective tissue diseases (systemic lupus erythematosus and systemic sclerosis)MANNUCCI, Pier Mannuccio; VANOLI, Massimo; FORZA, Ileana et al.Haematologica (Roma). 2003, Vol 88, Num 8, pp 914-918, issn 0390-6078, 5 p.Article

Changes in health and disease of the metalloprotease that cleaves von Willebrand factorMANNUCCI, Pier Mannuccio; CANCIANI, Maria Teresa; FORZA, Ileana et al.Blood. 2001, Vol 98, Num 9, pp 2730-2735, issn 0006-4971Article

Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand diseaseBARONCIANI, Luciano; COZZI, Giovanna; CANCIANI, Maria Teresa et al.Thrombosis and haemostasis. 2000, Vol 84, Num 4, pp 536-540, issn 0340-6245Article

Molecular characterization, recombinant protein expression, and mRNA analysis of type 3 von Willebrand disease: Studies of an Italian cohort of 10 patientsSOLIMANDO, Maria; BARONCIAN, Luciano; MARIA, Silvia La et al.American journal of hematology. 2012, Vol 87, Num 9, pp 870-874, issn 0361-8609, 5 p.Article

An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigreesKUNICKI, Thomas J; FEDERICI, Augusto B; SALOMON, Daniel R et al.Blood. 2004, Vol 104, Num 8, pp 2359-2367, issn 0006-4971, 9 p.Article

ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remissionPEYVANDI, Flora; LAVORETANO, Silvia; RETI, Marienn et al.Haematologica (Roma). 2008, Vol 93, Num 2, pp 232-239, issn 0390-6078, 8 p.Article

von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndromeREMUZZI, Giuseppe; GALBUSERA, Miriam; PERICO, Norberto et al.Blood. 2002, Vol 100, Num 3, pp 778-785, issn 0006-4971Article

The thrombospondin-1 N700S polymorphism is associated with early myocardial infarction without altering von willebrand factor multimer sizeZWICKER, Jeffrey I; PEYVANDI, Flora; MANNUCCI, Pier et al.Blood. 2006, Vol 108, Num 4, pp 1280-1283, issn 0006-4971, 4 p.Article

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