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Idiopathic thrombocytopenic purpura (ITP) in the elderly: clinical course in 178 patients.
Published in:
European Journal of Haematology, 2006, v. 76, n. 3, p. 210, doi. 10.1111/j.1600-0609.2005.00602.x
By:
- Bizzoni, L.;
- Mazzucconi, M. G.;
- Gentile, M.;
- Santoro, C.;
- Bernasconi, S.;
- Chiarotti, F.;
- Foà, R.;
- Mandelli, F.
Publication type:
Article
Letter to the editor: Level of protein s and essential thrombocythemia.
Published in:
American Journal of Hematology, 1991, v. 36, n. 1, p. 73, doi. 10.1002/ajh.2830360119
By:
- Mazzucconi, M. G.;
- Chistolini, A.;
- Ferrari, A.;
- Arcieri, P.;
- Mandelli, F.
Publication type:
Article
Letter to the editor: Level of protein s and essential thrombocythemia.
Published in:
American Journal of Hematology, 1990, v. 35, n. 2, p. 141, doi. 10.1002/ajh.2830350219
By:
- Mazzucconi, M. G.;
- Chistolini, A.;
- Ferrari, A.;
- Arcieri, P.;
- Mandelli, F.
Publication type:
Article
Evaluation of factor VII antigen in factor VII congenital deficiencies with a new ELISA assay.
Published in:
American Journal of Hematology, 1987, v. 26, n. 4, p. 313, doi. 10.1002/ajh.2830260404
By:
- Tirindelli, M. C.;
- Mariani, G.;
- Mazzucconi, M. G.;
- Iacopino, G.;
- Carbonaro, M.;
- Ghirardini, A.;
- Motta, M.;
- Mandelli, F.
Publication type:
Article
Evaluation of the nature of mildly prolonged prothrombin times.
Published in:
American Journal of Hematology, 1987, v. 24, n. 1, p. 37, doi. 10.1002/ajh.2830240106
By:
- Mazzucconi, M. G.;
- Mariani, G.;
- Chistolini, A.;
- Lasagni, R. Pasquali;
- Motta, M.;
- Ghirardini, A.;
- Altieri, D.;
- Mannucci, P. M.;
- Mandelli, F.
Publication type:
Article
Pipobroman therapy of essential thrombocythemia.
Published in:
European Journal of Haematology, 1986, v. 37, n. 4, p. 306, doi. 10.1111/j.1600-0609.1986.tb02317.x
By:
- Mazzucconi, M. G.;
- Francesconi, M.;
- Chistolini, A.;
- Falcione, E.;
- Ferrari, A.;
- Tirindelli, M. C.;
- Mandelli, F.
Publication type:
Article
Immune tolerance induction with a high purity von Willebrand factor/VIII complex concentrate in haemophilia A patients with inhibitors at high risk of a poor response.
Published in:
Haemophilia, 2007, v. 13, n. 4, p. 373, doi. 10.1111/j.1365-2516.2007.01484.x
By:
- GRINGERI, A.;
- MUSSO, R.;
- MAZZUCCONI, M. G.;
- PISEDDU, G.;
- SCHIAVONI, M.;
- PIGNOLONI, P.;
- MANNUCCI, P. M.
Publication type:
Article
Clinical efficacy of highly purified, doubly virus-inactivated factor VIII/von Willebrand factor concentrate (Fanhdi® ) in the treatment of von Willebrand disease: a retrospective clinical study.
Published in:
Haemophilia, 2002, v. 8, n. 6, p. 761, doi. 10.1046/j.1365-2516.2002.00688.x
By:
- Federici, A. B.;
- Baudo, F.;
- Caracciolo, C.;
- Mancuso, G.;
- Mazzucconi, M. G.;
- Musso, R.;
- Schinco, P. C.;
- Targhetta, R.;
- Mannucci, P. Mannuccio
Publication type:
Article
Postpartum inhibitor to factor VIII: treatment with high-dose immunoglobulin and dexamethasone.
Published in:
Haemophilia, 2001, v. 7, n. 4, p. 422, doi. 10.1046/j.1365-2516.2001.00529.x
By:
- Mazzucconi, M. G.;
- Bizzoni, L.;
- Giorgi, A.;
- Morano, S. G.;
- Peraino, M.;
- Russo, M.;
- Alimena, G.
Publication type:
Article
A CRM-Positive Variant of Factor-VII Deficiency and the Detection of Heterozygotes with the Assay of Factor-like Antigen.
Published in:
British Journal of Haematology, 1977, v. 36, n. 1, p. 127, doi. 10.1111/j.1365-2141.1977.tb05762.x
By:
- Mazzucconi, M. G.;
- Mandelli, F.;
- Mariani, G.;
- Briët, E.;
- Veltkamp, J. J.
Publication type:
Article
Pattern of bleeding in a large prospective cohort of haemophilia A patients: A three‐year follow‐up of the AHEAD (Advate in HaEmophilia A outcome Database) study.
Published in:
Haemophilia, 2018, v. 24, n. 1, p. 85, doi. 10.1111/hae.13361
By:
- Khair, K.;
- Mazzucconi, M. G.;
- Parra, R.;
- Santagostino, E.;
- Tsakiris, D. A.;
- Hermans, C.;
- Oldenburg, J.;
- Spotts, G.;
- Steinitz‐Trost, K.;
- Gringeri, A.
Publication type:
Article
Anticoagulant therapy in patients with Glanzmann's Thrombasthenia: Is it possible?
Published in:
Haemophilia, 2017, v. 23, n. 6, p. e531, doi. 10.1111/hae.13350
By:
- Ferretti, A.;
- Santoro, C.;
- Ferrara, G.;
- Baldacci, E.;
- Barone, F.;
- Mazzucconi, M. G.
Publication type:
Article
Correlation between FIX genotype and pharmacokinetics of Nonacog alpha according to a multicentre Italian study.
Published in:
Haemophilia, 2016, v. 22, n. 4, p. 537, doi. 10.1111/hae.12916
By:
- Morfini, M.;
- Dragani, A.;
- Paladino, E.;
- Radossi, P.;
- Di Minno, G.;
- Mazzucconi, M. G.;
- Rossetti, G.;
- Barillari, G.;
- Napolitano, M.;
- Tagariello, G.
Publication type:
Article
Bleeding phenotype and correlation with factor XI (FXI) activity in congenital FXI deficiency: results of a retrospective study from a single centre.
Published in:
Haemophilia, 2015, v. 21, n. 4, p. 496, doi. 10.1111/hae.12628
By:
- Santoro, C.;
- Di Mauro, R.;
- Baldacci, E.;
- De Angelis, F.;
- Abbruzzese, R.;
- Barone, F.;
- Bochicchio, R. A.;
- Ferrara, G.;
- Guarini, A.;
- Foà, R.;
- Mazzucconi, M. G.
Publication type:
Article
Prevalence of allo-immunization anti-HLA and anti-integrin αIIbβ3 in Glanzmann Thromboasthenia patients.
Published in:
Haemophilia, 2010, v. 16, n. 5, p. 805, doi. 10.1111/j.1365-2516.2010.02230.x
By:
- SANTORO, C.;
- RAGO, A.;
- BIONDO, F.;
- CONTI, L.;
- PULCINELLI, F.;
- LAURENTI, L.;
- PERRONE, M. P.;
- BALDACCI, E.;
- LEPORACE, A.;
- MAZZUCCONI, M. G.
Publication type:
Article
Mortality and causes of death in Italian persons with haemophilia, 1990-2007.
Published in:
Haemophilia, 2010, v. 16, n. 3, p. 437, doi. 10.1111/j.1365-2516.2009.02188.x
By:
- TAGLIAFERRI, A.;
- RIVOLTA, G. F.;
- IORIO, A.;
- OLIOVECCHIO, E.;
- MANCUSO, M. E.;
- MORFINI, M.;
- ROCINO, A.;
- MAZZUCCONI, M. G.;
- FRANCHINI, M.
Publication type:
Article
Efficacy and safety of highly purified, doubly virus-inactivated VWF/FVIII concentrates in inherited von Willebrand’s disease: results of an Italian cohort study on 120 patients characterized by bleeding severity score.
Published in:
Haemophilia, 2010, v. 16, n. 1, p. 101, doi. 10.1111/j.1365-2516.2009.02088.x
By:
- FEDERICI, A. B.;
- BARILLARI, G.;
- ZANON, E.;
- MAZZUCCONI, M. G.;
- MUSSO, R.;
- TARGHETTA, R.;
- MANNUCCI, P. M.
Publication type:
Article
Performance of recalibrated ReFacto® laboratory standard in the measurement of FVIII plasma concentration via the chromogenic and one-stage assays after infusion of recalibrated ReFacto® (B-domain deleted recombinant factor VIII)
Published in:
Haemophilia, 2009, v. 15, n. 3, p. 779, doi. 10.1111/j.1365-2516.2009.01983.x
By:
- SANTORO, C.;
- IORIO, A.;
- FERRANTE, F.;
- PALLOTTA, A.;
- PIGNOLONI, P.;
- BIONDO, F.;
- AGNELLI, G.;
- MAZZUCCONI, M. G.
Publication type:
Article
RECOMBINANT ALPHA 2b INTERFERON IN THE TREATMENT OF REFRACTORY AUTOIMMUNE THROMBOCYTOPENIC PURPURA.
Published in:
British Journal of Haematology, 1992, v. 80, n. 3, p. 416, doi. 10.1111/j.1365-2141.1992.tb08157.x
By:
- Chtstolini, A.;
- Mazzucconi, M. G.;
- Dragoni, F.;
- Sanctis, V. De;
- Mandelli, F.
Publication type:
Article
Carrier detection in factor VII congenital deficiency.
Published in:
British Journal of Haematology, 1985, v. 60, n. 4, p. 687, doi. 10.1111/j.1365-2141.1985.tb07473.x
By:
- Mariani, G.;
- Hermans, J.;
- Orlando, M.;
- Mazzucconi, M. G.;
- Ciavarella, N.;
- Faiella, A.;
- Berrettini, M.;
- Chistolini, A.;
- Di Nucci, G. D.;
- Mannucci, P. M.;
- Mandelli, F.
Publication type:
Article
Factor VII Deficiency: Immunological Characterization of Genetic Variants and Detection of Carriers.
Published in:
British Journal of Haematology, 1981, v. 48, n. 1, p. 7, doi. 10.1111/j.1365-2141.1981.00007.x
By:
- Mariani, G.;
- Mazzucconi, M. G.;
- Hermans, J.;
- Ciavarella, N.;
- Faiella, A.;
- Hassan, H. J.;
- Mannucci, P. M.;
- Nenci, G. G.;
- Orlando, M.;
- Romoli, D.;
- Mandelli, F.
Publication type:
Article

Found: 21

Idiopathic thrombocytopenic purpura (ITP) in the elderly: clinical course in 178 patients.

Letter to the editor: Level of protein s and essential thrombocythemia.

Letter to the editor: Level of protein s and essential thrombocythemia.

Evaluation of factor VII antigen in factor VII congenital deficiencies with a new ELISA assay.

Evaluation of the nature of mildly prolonged prothrombin times.

Pipobroman therapy of essential thrombocythemia.

Immune tolerance induction with a high purity von Willebrand factor/VIII complex concentrate in haemophilia A patients with inhibitors at high risk of a poor response.

Clinical efficacy of highly purified, doubly virus-inactivated factor VIII/von Willebrand factor concentrate (Fanhdi<sup>®</sup> ) in the treatment of von Willebrand disease: a retrospective clinical study.

Postpartum inhibitor to factor VIII: treatment with high-dose immunoglobulin and dexamethasone.

A CRM-Positive Variant of Factor-VII Deficiency and the Detection of Heterozygotes with the Assay of Factor-like Antigen.

Pattern of bleeding in a large prospective cohort of haemophilia A patients: A three‐year follow‐up of the AHEAD (Advate in HaEmophilia A outcome Database) study.

Anticoagulant therapy in patients with Glanzmann's Thrombasthenia: Is it possible?

Correlation between FIX genotype and pharmacokinetics of Nonacog alpha according to a multicentre Italian study.

Bleeding phenotype and correlation with factor XI (FXI) activity in congenital FXI deficiency: results of a retrospective study from a single centre.

Prevalence of allo-immunization anti-HLA and anti-integrin αIIbβ3 in Glanzmann Thromboasthenia patients.

Mortality and causes of death in Italian persons with haemophilia, 1990-2007.

Efficacy and safety of highly purified, doubly virus-inactivated VWF/FVIII concentrates in inherited von Willebrand’s disease: results of an Italian cohort study on 120 patients characterized by bleeding severity score.

Performance of recalibrated ReFacto<sup>®</sup> laboratory standard in the measurement of FVIII plasma concentration via the chromogenic and one-stage assays after infusion of recalibrated ReFacto<sup>®</sup> (B-domain deleted recombinant factor VIII)

RECOMBINANT ALPHA 2b INTERFERON IN THE TREATMENT OF REFRACTORY AUTOIMMUNE THROMBOCYTOPENIC PURPURA.

Carrier detection in factor VII congenital deficiency.

Factor VII Deficiency: Immunological Characterization of Genetic Variants and Detection of Carriers.