GIROLAMI, ANTONIO

GIROLAMI, ANTONIO  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
"Anti-platelet antibodies" in HIV infected haemophiliacs. 1990 FABRIS, FABRIZIOCASONATO, SANDRAGIROLAMI, ANTONIO + FOLIA HAEMATOLOGICA - -
"Pseudo homozygous" activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: report of two cases belonging to two unrelated kindreds. 1996 SIMIONI, PAOLOGAVASSO, SABRINATORMENE, DANIELAGIROLAMI, ANTONIO + THROMBOSIS AND HAEMOSTASIS - -
. Isolation and characterization of an antifactor V antibody causing APC resistance from a patient with severe thrombotic manifestations 2002 SIMIONI, PAOLOTORMENE, DANIELAGIROLAMI, ANTONIO + BLOOD - -
1-Desamino-8-D-arginine vasopressin (DDAVP) infusion in type IIB von Willebrand's disease: shortening of bleeding time and induction of a variable pseudothrombocytopenia. 1990 CASONATO, SANDRAGIROLAMI, ANTONIO + THROMBOSIS AND HAEMOSTASIS - -
75SE-methoinine platelet survival studies: a proposal for a mathematical correction of the curve 1982 FABRIS, FABRIZIOCASONATO, SANDRARANDI, MARIA LUIGIAGIROLAMI, ANTONIO + HAEMOSTASIS - -
[Coagulation factors and blood platelets. (Presence and location of factor VIII and of fibrinogen in normal human platelets and in patients with coagulation disorders, using an immunofluorescence technic)]. 1979 FABRIS, FABRIZIOBETTERLE, CORRADOCASONATO, SANDRAGIROLAMI, ANTONIO + LA RICERCA IN CLINICA E IN LABORATORIO - -
[Factor XIII deficiency due to lack of both the S and A subunits. (Classification of factor XIII deficiency in 2 groups)]. 1979 GIROLAMI, ANTONIOBETTERLE, CORRADOCASONATO, SANDRA + LA RICERCA IN CLINICA E IN LABORATORIO - -
[The genetics of thrombosis]. 1991 GIROLAMI, ANTONIOSIMIONI, PAOLO + HAEMATOLOGICA - -
A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding 2020 Girolami A.Cosi E. + JOURNAL OF THROMBOSIS AND THROMBOLYSIS - -
A critical evaluation of the available methods for the determination of factor VIII von Willebrand. 1986 CASONATO, SANDRAGIROLAMI, ANTONIO FOLIA HAEMATOLOGICA - -
A dysfunctional factor X (factor X San Giovanni Rotondo) present at homozygous and double heterozygous level: Identification of a novel microdeletion (delC556) and missense mutation (Lys(408)-> Asn) in the factor X gene - A study of an Italian family 2001 SIMIONI, PAOLOVIANELLO, FABRIZIOBARZON, LUISADAL BELLO, FEDERICOPALU', GIORGIOGIROLAMI, ANTONIO + THROMBOSIS RESEARCH - -
A family with an abnormal protein C and a thrombotic tendency. 1993 GIROLAMI, ANTONIOSIMIONI, PAOLOPRANDONI, PAOLO + HAEMATOLOGIA - -
A family with factor x deficiency from Argentina: a compound heterozygosis due to the combination of a new mutation (Gln138Arg) with an already known one (Glu350Lys) 2016 GIROLAMI, ANTONIOMolina, MaFERRARI, SILVIASAMBADO, LUISA + BLOOD COAGULATION & FIBRINOLYSIS - -
A forgotten or minimized head trauma, rather than a mild FVII deficiency, is the most likely cause of a subdural hematoma 2016 GIROLAMI, ANTONIOFERRARI, SILVIACOSI, ELISABETTALombardi, A. M. Blood Cells, Molecules and Diseases - -
A frequent factor XII gene mutation in Hageman trait. 1988 CASONATO, SANDRAGIROLAMI, ANTONIO + HUMAN GENETICS - -
A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders 2001 SIMIONI, PAOLOSIMIONI, PAOLOGIROLAMI, ANTONIO + BRITISH JOURNAL OF HAEMATOLOGY - -
A microplate enzyme-linked immunospecific assay (ELISA) detecting unbound anti-platelet antibodies. 1984 FABRIS, FABRIZIOCASONATO, SANDRAGIROLAMI, ANTONIO + FOLIA HAEMATOLOGICA - -
A new congenital platelet abnormality characterized by spontaneous platelet aggregation, enhanced von Willebrand factor platelet interaction, and the presence of all von Willebrand factor multimers in plasma. 1989 CASONATO, SANDRAFABRIS, FABRIZIOGIROLAMI, ANTONIO + BLOOD - -
A new ELISA method for the detection of serum bindable anti-platelet antibodies (SPBIG). 1985 FABRIS, FABRIZIOCASONATO, SANDRAGIROLAMI, ANTONIO + CLINICA CHIMICA ACTA - -
A new Factor X defect (Factor X Padua 3) A compound heterozygous between true deficiency (Gly 380-Arg) and an abnormality (Der334 -Pro) 2001 VIANELLO, FABRIZIOLOMBARDI, ANNA-MARIAGIROLAMI, ANTONIO + THROMBOSIS RESEARCH - -