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Journal Articles

Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413Gln

Subject Area:

Hematology , Oncology

Antonio Girolami, Mariano Paoletti, Silvia Ferrari, Diana Garcia

Acta Haematol (2021) 144 (1): 100–104.

https://doi.org/10.1159/000507071

Published Online: 12 May 2020

View article titled, Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413Gln

Journal Articles

Abnormal Factor X (Factor X Friuli) Coagulation Disorder. The Heterozygote Population: A Study of 57 Subjects

Subject Area:

Hematology , Oncology

Antonio Girolami, Adriano Brunetti, Giovanna Bareggi, Giuseppe Cella

Acta Haematol (1974) 51 (1): 40–50.

https://doi.org/10.1159/000208273

Published Online: 04 March 2009

View article titled, Abnormal Factor X (Factor X Friuli) Coagulation Disorder. The Heterozygote Population: A Study of 57 Subjects

Journal Articles

Normal Factor VIII Antigen Level in Combined Congenital Deficiency of Factor V and Factor VIII

Subject Area:

Hematology , Oncology

Antonio Girolami, Giovanna Bareggi

Acta Haematol (1974) 51 (6): 362–363.

https://doi.org/10.1159/000208319

Published Online: 04 March 2009

View article titled, Normal Factor VIII Antigen Level in Combined Congenital Deficiency of Factor V and Factor VIII

Journal Articles

Platelet Aggregation and Adhesiveness in Classical Factor X Deficiency and in the Abnormal Factor X (Factor X Friuli) Coagulation Disorder

Subject Area:

Hematology , Oncology

Antonio Girolami, Fabrizio Fabris, Renata Peruffo, Paolo Coser

Acta Haematol (1976) 56 (5): 307–313.

https://doi.org/10.1159/000207952

Published Online: 03 March 2009

View article titled, Platelet Aggregation and Adhesiveness in Classical Factor X Deficiency and in the Abnormal Factor X (Factor X Friuli) Coagulation Disorder

Journal Articles

Congenital Deficiency of Factor XIII with Normal Subunit S and Lack of Subunit A: Report of a New Family

Subject Area:

Hematology , Oncology

Antonio Girolami, Alessandro Burul, Antonio Sticchi

Acta Haematol (1977) 58 (1): 17–26.

https://doi.org/10.1159/000207801

Published Online: 03 March 2009

View article titled, Congenital Deficiency of Factor XIII with Normal Subunit S and Lack of Subunit A: Report of a New Family

Journal Articles

Factor X Friuli Coagulation Disorder: Report of a Newly Recognized Patient and Some Considerations on the Frequency of the Disease in the Friuli Area

Subject Area:

Hematology , Oncology

Antonio Girolami, Roberto Falomo, Luigino de Marco, Giovanni Patrassi

Acta Haematol (1976) 56 (1): 27–38.

https://doi.org/10.1159/000207916

Published Online: 03 March 2009

View article titled, Factor X Friuli Coagulation Disorder: Report of a Newly Recognized Patient and Some Considerations on the Frequency of the Disease in the Friuli Area

Journal Articles

The Effect of lonophore on Platelet Aggregation in von Willebrand’s Disease and in Congenital Afibrinogenemia. A Comparison with Ristocetin

Subject Area:

Hematology , Oncology

Antonio Girolami, Fabrizio Fabris, Luigino de Marco, Renata Peruffo

Acta Haematol (1976) 56 (3): 151–159.

https://doi.org/10.1159/000207932

Published Online: 03 March 2009

View article titled, The Effect of lonophore on Platelet Aggregation in von Willebrand’s Disease and in Congenital Afibrinogenemia. A Comparison with Ristocetin

Journal Articles

Considerations on Combined Factor VII and Factor VIII Defect

Subject Area:

Hematology , Oncology

Antonio Girolami, Giovanni M. Patrassi, Renzo Dal Boanon

Acta Haematol (1981) 65 (2): 140–141.

https://doi.org/10.1159/000207167

Published Online: 27 February 2009

View article titled, Considerations on Combined Factor VII and Factor VIII Defect

Journal Articles

The Congenital Variants of the Prothrombin Complex Factors

Subject Area:

Hematology , Oncology

Antonio Girolami

Acta Haematol (1980) 63 (6): 339–341.

https://doi.org/10.1159/000207434

Published Online: 27 February 2009

View article titled, The Congenital Variants of the Prothrombin Complex Factors

Journal Articles

Thrombocytopenia Secondary to Oxprenolol, a β-Blocking Agent

Subject Area:

Hematology , Oncology

Giovanni M. Patrassi, Alessandra Casonato, Fabrizio Fabris, Antonio Girolami

Acta Haematol (1982) 68 (1): 75–76.

https://doi.org/10.1159/000206955

Published Online: 26 February 2009

View article titled, Thrombocytopenia Secondary to Oxprenolol, a β-Blocking Agent

Journal Articles

Clinical Significance of Beta-Thromboglobulin in Patients with High Platelet Count

Subject Area:

Hematology , Oncology

Fabrizio Fabris, Maria Luigia Randi, Alessandra Casonato, Renzo Dal Bo Zanon, Pietro Bonvicini, Antonio Girolami

Acta Haematol (1984) 71 (1): 32–38.

https://doi.org/10.1159/000206503

Published Online: 25 February 2009

View article titled, Clinical Significance of Beta-Thromboglobulin in Patients with High Platelet Count

Journal Articles

Bernard-Soulier Syndrome: Diagnosis by an ELISA Method Using Monoclonal Antibodies in 2 New Unrelated Patients

Subject Area:

Hematology , Oncology

Luigi De Marco, Fabrizio Fabris, Alessandra Casonato, Pietro Fabris, Maria Grazia Dal Ben, Antonio Barbato, Antonio Girolami

Acta Haematol (1986) 75 (4): 203–208.

https://doi.org/10.1159/000206125

Published Online: 25 February 2009

View article titled, Bernard-Soulier Syndrome: Diagnosis by an ELISA Method Using Monoclonal Antibodies in 2 New Unrelated Patients

Journal Articles

Tentative and Updated Classification of Factor X Variants

Subject Area:

Hematology , Oncology

Antonio Girolami

Acta Haematol (1986) 75 (1): 58–59.

https://doi.org/10.1159/000206084

Published Online: 25 February 2009

View article titled, Tentative and Updated Classification of Factor X Variants

Journal Articles

Thromboembolism and Factor VII Defect

Subject Area:

Hematology , Oncology

Antonio Girolami

Acta Haematol (1984) 72 (5): 357–358.

https://doi.org/10.1159/000206416

Published Online: 25 February 2009

View article titled, Thromboembolism and Factor VII Defect

Journal Articles

Acquired Type I von Willebrand’s Disease in a Patient with Essential Thrombocytosis

Subject Area:

Hematology , Oncology

Alessandra Casonato, Fabrizio Fabris, Lucia Zancan, Antonio Girolami

Acta Haematol (1986) 75 (3): 188–189.

https://doi.org/10.1159/000206119

Published Online: 25 February 2009

View article titled, Acquired Type I von Willebrand’s Disease in a Patient with Essential Thrombocytosis

Journal Articles

Response to Splenectomy in Idiopathic Thrombocytopenic Purpura: Prognostic Value of the Clinical and Laboratory Evaluation

Subject Area:

Hematology , Oncology

Fabrizio Fabris, Nello Zanatta, Alessandra Casonato, Maria Luigia Randi, Guido Luzzatto, Antonio Girolami

Acta Haematol (1989) 81 (1): 28–33.

https://doi.org/10.1159/000205407

Published Online: 24 February 2009

View article titled, Response to Splenectomy in Idiopathic Thrombocytopenic Purpura: Prognostic Value of the Clinical and Laboratory Evaluation

Journal Articles

Bilateral Ileofemoral Thrombophlebitis after Ten Contraceptive Pills in a 25-Year-Old Woman with Antithrombin III Deficiency

Subject Area:

Hematology , Oncology

Antonio Girolami, Francesco Stevanato, Anna Rosa Lazzaro

Acta Haematol (1988) 79 (2): 118–119.

https://doi.org/10.1159/000205738

Published Online: 24 February 2009

View article titled, Bilateral Ileofemoral Thrombophlebitis after Ten Contraceptive Pills in a 25-Year-Old Woman with Antithrombin III Deficiency

Journal Articles

Thrombocytopenia in HIV-Infected Hemophiliacs

Subject Area:

Hematology , Oncology

Fabrizio Fabris, Michele Mussap, Antonio Girolami

Acta Haematol (1989) 81 (4): 219–220.

https://doi.org/10.1159/000205566

Published Online: 24 February 2009

View article titled, Thrombocytopenia in HIV-Infected Hemophiliacs

Journal Articles

Lithium Carbonate Failed to Modify the Neutropenia Associated with Large Granular Lymphocyte Proliferation

Subject Area:

Hematology , Oncology

Dino Sgarabotto, Francesco Dazzi, Antonio Girolami

Acta Haematol (1989) 81 (2): 114–115.

https://doi.org/10.1159/000205539

Published Online: 24 February 2009

View article titled, Lithium Carbonate Failed to Modify the Neutropenia Associated with Large Granular Lymphocyte Proliferation

Journal Articles

Factor VIII/von Willebrand Factor Abnormalities during L -Asparaginase Treatment in Patients with Acute Lymphoblastic Leukemia

Subject Area:

Hematology , Oncology

Alessandra Casonato, Anna Rosa Lazzaro, Angelo Rosolen, Antonio Girolami

Acta Haematol (1988) 80 (4): 190–193.

https://doi.org/10.1159/000205635

Published Online: 24 February 2009

View article titled, Factor VIII/von Willebrand Factor Abnormalities during L -Asparaginase Treatment in Patients with Acute Lymphoblastic Leukemia

NARROW

Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413Gln

Abnormal Factor X (Factor X Friuli) Coagulation Disorder. The Heterozygote Population: A Study of 57 Subjects

Normal Factor VIII Antigen Level in Combined Congenital Deficiency of Factor V and Factor VIII

Platelet Aggregation and Adhesiveness in Classical Factor X Deficiency and in the Abnormal Factor X (Factor X Friuli) Coagulation Disorder

Congenital Deficiency of Factor XIII with Normal Subunit S and Lack of Subunit A: Report of a New Family

Factor X Friuli Coagulation Disorder: Report of a Newly Recognized Patient and Some Considerations on the Frequency of the Disease in the Friuli Area

The Effect of lonophore on Platelet Aggregation in von Willebrand’s Disease and in Congenital Afibrinogenemia. A Comparison with Ristocetin

Considerations on Combined Factor VII and Factor VIII Defect

The Congenital Variants of the Prothrombin Complex Factors

Thrombocytopenia Secondary to Oxprenolol, a β-Blocking Agent

Clinical Significance of Beta-Thromboglobulin in Patients with High Platelet Count

Bernard-Soulier Syndrome: Diagnosis by an ELISA Method Using Monoclonal Antibodies in 2 New Unrelated Patients

Tentative and Updated Classification of Factor X Variants

Thromboembolism and Factor VII Defect

Acquired Type I von Willebrand’s Disease in a Patient with Essential Thrombocytosis

Response to Splenectomy in Idiopathic Thrombocytopenic Purpura: Prognostic Value of the Clinical and Laboratory Evaluation

Bilateral Ileofemoral Thrombophlebitis after Ten Contraceptive Pills in a 25-Year-Old Woman with Antithrombin III Deficiency

Thrombocytopenia in HIV-Infected Hemophiliacs

Lithium Carbonate Failed to Modify the Neutropenia Associated with Large Granular Lymphocyte Proliferation

Factor VIII/von Willebrand Factor Abnormalities during L -Asparaginase Treatment in Patients with Acute Lymphoblastic Leukemia

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