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Journal Articles

Molecular Mechanisms of FVII Deficiency: Expression of Mutations Clustered in the IVS7 Donor Splice Site of Factor VII Gene

M. Pinotti, R. Toso, R. Redaelli, M. Berrettini, G. Marchetti, F. Bernardi

Blood (1998) 92 (5): 1646–1651.

https://doi.org/10.1182/blood.V92.5.1646

Published: 1998

Journal Articles

A Factor V Genetic Component Differing From Factor V R506Q Contributes to the Activated Protein C Resistance Phenotype

F. Bernardi, E.M. Faioni, E. Castoldi, B. Lunghi, G. Castaman, E. Sacchi, P.M. Mannucci

Blood (1997) 90 (4): 1552–1557.

https://doi.org/10.1182/blood.V90.4.1552

Published: 1997

Journal Articles

The Ser460Pro substitution of the protein S (PS) gene in rare in Italian patients with type IIa PS deficiency [letter]

G Castaman, M Ruggeri, A Tosetto, F Bernardi, F Rodeghiero

Blood (1996) 88 (9): 3666–3667.

https://doi.org/10.1182/blood.V88.9.3666.bloodjournal8893666

Published: 1996

Journal Articles

Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategy

CJ Formstone, AI Wacey, LP Berg, S Rahman, D Bevan, M Rowley, J Voke, F Bernardi, C Legnani, P Simioni

Blood (1995) 86 (7): 2632–2641.

https://doi.org/10.1182/blood.V86.7.2632.2632

Published: 1995

Journal Articles

Improved cytogenetics in multiple myeloma: a study of 151 patients including 117 patients at diagnosis

JL Lai, M Zandecki, JY Mary, F Bernardi, V Izydorczyk, M Flactif, P Morel, JP Jouet, F Bauters, T Facon

Blood (1995) 85 (9): 2490–2497.

https://doi.org/10.1182/blood.V85.9.2490.bloodjournal8592490

Published: 1995

Journal Articles

A de novo and heterozygous gene deletion causing a variant of von Willebrand disease

F Bernardi, G Marchetti, S Guerra, A Casonato, D Gemmati, P Patracchini, G Ballerini, F Conconi

Blood (1990) 75 (3): 677–683.

https://doi.org/10.1182/blood.V75.3.677.677

Published: 1990

Journal Articles

Partial gene deletion in a family with factor X deficiency

F Bernardi, G Marchetti, P Patracchini, S Volinia, D Gemmati, P Simioni, A Girolami

Blood (1989) 73 (8): 2123–2127.

https://doi.org/10.1182/blood.V73.8.2123.2123

Published: 1989

Journal Articles

Factor XII gene alteration in Hageman trait detected by TaqI restriction enzyme

F Bernardi, G Marchetti, P Patracchini, L del Senno, M Tripodi, A Fantoni, S Bartolai, F Vannini, L Felloni, L Rossi

Blood (1987) 69 (5): 1421–1424.

https://doi.org/10.1182/blood.V69.5.1421.1421

Published: 1987

NARROW

Molecular Mechanisms of FVII Deficiency: Expression of Mutations Clustered in the IVS7 Donor Splice Site of Factor VII Gene

A Factor V Genetic Component Differing From Factor V R506Q Contributes to the Activated Protein C Resistance Phenotype

The Ser460Pro substitution of the protein S (PS) gene in rare in Italian patients with type IIa PS deficiency [letter]

Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategy

Improved cytogenetics in multiple myeloma: a study of 151 patients including 117 patients at diagnosis

A de novo and heterozygous gene deletion causing a variant of von Willebrand disease

Partial gene deletion in a family with factor X deficiency

Factor XII gene alteration in Hageman trait detected by TaqI restriction enzyme

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American Society of Hematology

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ASH Publications

American Society of Hematology

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