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Mostrati risultati da 1 a 20 di 52
Titolo Data di pubblicazione Autori Tipo File Abstract
Allele Frequency of CYP2C9 Gene Polymorphisms in Iran 2002 F. PeyvandiM. SpreaficoP.M. Mannucci + Article (author) -
Warfarin and acenocoumarol dose requirements according to CYP2C9 genotyping in North-Italian patients 2003 M. SpreaficoF. PeyvandiP.M. Mannucci + Article (author) -
CYP2C9 genotypes and dose requirements during the induction phase of oral anticoagulant therapy 2004 F. PeyvandiM. SpreaficoS.M. SiboniP.M. Mannucci + Article (author) -
International Registry of rare bleeding disorders (RBD) 2004 F. PeyvandiM. SpreaficoM. MenegattiI. M. GaragiolaL. TagliabueP. M. Mannucci Article (author) -
Relationship between CYP2C9 and VKORC1 polymorphisms and anticoagulant dose requirement 2005 M. SpreaficoF. PeyvandiP.M. Mannucci + Article (author) -
Relationship between CYP2C9 and VKORC1 polymorphisms and anticoagulant dose requirement 2005 M. SpreaficoF. PeyvandiP.M. Mannucci + Conference Object -
Factor V and combined factor V and VIII deficiencies 2005 F. PeyvandiM. Spreafico Book Part (author) -
Molecular characterization in an Italian patient with plasminogen deficiency and ligneous conjunctivitis 2005 S.M. SiboniM. SpreaficoM. MenegattiF. Peyvandi + Article (author) -
International Rare Bleeding Disorders Database 2005 F. PeyvandiR. PallaM, MenegattiI. GaragiolaS. M. SiboniP. M. MannucciM. SpreaficoL. TagliabueS. Lavoretano + Multimedia Object (author) -
Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII 2005 M. SpreaficoI. GaragiolaF. Peyvandi + Article (author) -
Molecular characterization in an Italian patient with plasminogen deficiency and ligneous conjunctivitis 2005 S.M. SiboniM. SpreaficoM. MenegattiF. Peyvandi + Conference Object -
Future perspective of international registry on rare inherited bleeding disorder 2006 F. PeyvandiM. SpreaficoM. MenegattiR. PallaS. M. SiboniP. M. Mannucci Article (author) -
Future perspective of international registry on rare inherited bleeding disorder 2006 F. PeyvandiM. SpreaficoR. PallaS. M. SiboniP. M. Mannucci + Article (author) -
Rare bleeding disorders 2006 F. PeyvandiM. SpreaficoM. MenegattiR. PallaS. SiboniP.M. Mannucci + Article (author) -
Genetics of rare bleeding disorders 2006 F. PeyvandiI. M. GaragiolaS. LavoretanoM. MenegattiR. PallaM. SpreaficoL. TagliabueS. DugaP. M. Mannucci Conference Object -
Genetic diagnosis of haemophilia and other inherited bleeding disorders 2006 F. PeyvandiI. GaragiolaS. LavoretanoM. MenegattiR. PallaM. SpreaficoL. TagliabueR. AsseltaS. DugaP.M. Mannucci + Article (author) -
Coagulation factor V gene analysis in five Indian patients : identification of three novel small deletions 2006 R. AsseltaS. DugaM. SpreaficoM.L. Tenchini + Article (author) -
Patients Informative Booklet on the Women with rare bleeding disorders project 2007 F. PeyvandiM. SpreaficoR. PallaS. LavoretanoI. GaragiolaS.M. Siboni Working Paper -
Molecular characterization of an Italian patient with plasminogen deficiency and ligneous conjunctivitis 2007 S.M. SiboniM. SpreaficoM. MenegattiF. Peyvandi + Article (author) -
Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India 2007 M. SpreaficoF. Peyvandi + Article (author) -
Mostrati risultati da 1 a 20 di 52
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