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Mostrati risultati da 1 a 20 di 703
Titolo Data di pubblicazione Autori Tipo File Abstract
Mutant factor V (A19506GIn) in healthy centenarians 1996 P.M. MannucciF. PeyvandiD. Mari + Article (author) -
Factor V (Arg 506-->Gln) mutation in young survivors of myocardial infarction 1996 F. PeyvandiE. ColombiP.M. Mannucci + Article (author) -
Autoimmune protein S deficiency and deep vein thrombosis after chickenpox 1996 F. PeyvandiE. Faioni + Article (author) -
Frequency of factor V Arg506 Gln in Italians 1996 P.M. MannucciF. PeyvandiL. TagliabueG. MeratiM. Cattaneo + Article (author) -
Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency 1997 F. PeyvandiP.M. Mannucci + Article (author) -
The G1456 to T mutation in the thrombomodulin gene is not frequent in patients with venous thrombosis 1997 E.M. FaioniG. MeratiF. PeyvandiP.M. Mannucci + Article (author) -
Gene polymorphisms predicting high plasma levels of coagulation and fibrinolysis proteins. A study in centenarians 1997 P.M. MannucciD. MariG. MeratiF. PeyvandiL. Tagliabue + Article (author) -
Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients 1998 F. PeyvandiP.M. Mannucci + Article (author) -
Symptoms of inherited factor V deficiency in 35 Iranian patients 1998 F. PeyvandiP.M. Mannucci + Article (author) -
Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII 1998 F. PeyvandiP.M. Mannucci + Article (author) -
Characterization of two naturally occurring mutations in the second Epidermal Growth Factor-like domain of factor VII 1999 F. Peyvandi + Article (author) -
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency. Blood 1999 F. Peyvandi + Article (author) -
Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia 1999 F. PeyvandiP.M. Mannucci + Article (author) -
Detection of DNA by silver staining 1999 F. Peyvandi + Book Part (author) -
Rare coagulation disorders 1999 F. PeyvandiP.M. Mannucci Article (author) -
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease 2000 F. PeyvandiP.M. Mannucci + Article (author) -
Apparently dominant transmission of a recessive disease: deficiency of factor VII in Iranian Jews 2000 L. TagliabueF. Peyvandi + Article (author) -
Homozygous 2bp deletion in the human factor VII gene : a non-lethal mutation that is associated with a complete absence of circulating factor VII 2000 F. PeyvandiP.M. Mannucci + Article (author) -
Molecular characterization and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency 2000 F. PeyvandiP.M. Mannucci + Article (author) -
Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease 2000 L. BaroncianiF. PeyvandiA.B. Federici + Article (author) -
Mostrati risultati da 1 a 20 di 703
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