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Factor X Padua: A ‘New’ Congenital Factor X Abnormality with a Defect Only in the Extrinsic System

Acta Haematol (1985) 73 (1): 31–36.
This article has been cited by the following articles in journals that are participating in CrossRef Cited-by Linking.
A Rare Cause of Isolated Prothrombin Time Prolongation: Congenital Factor X Deficiency
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Journal of Pediatric Hematology/Oncology (2021) 43 (8): e1248.
A rare presentation of homozygous factor X deficiency in a pregnant patient: A case report and review of the literature
  • Marie‐Astrid van Dievoet
  • Marc Jacquemin
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Haemophilia (2019) 25 (1)
Factor X Friuli Coagulation Disorder: Almost 50 Years Later
  • Antonio Girolami
  • Elisabetta Cosi
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Clinical and Applied Thrombosis/Hemostasis (2018) 24 (1): 33.
Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years)
  • Antonio Girolami
  • Elisabetta Cosi
  • Claudia Santarossa
  • Silvia Ferrari
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European Journal of Haematology (2016) 97 (6): 547.
A family with factor X deficiency from Argentina
  • Antonio Girolami
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Blood Coagulation & Fibrinolysis (2016) 27 (6): 732.
Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology era
  • A. GIROLAMI
  • S. VETTORE
  • P. SCARPARO
  • A. M. LOMBARDI
Haemophilia (2011) 17 (1): 17.
Unexplained Discrepancies in the Activity—Antigen Ratio in Congenital FX Deficiencies With Defects in the Catalytic Domain
  • A. Girolami
  • P. Scarparo
  • S. Vettore
  • N. Candeo
  • R. Scandellari
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Clinical and Applied Thrombosis/Hemostasis (2009) 15 (6): 621.
Different genotypes are responsible for the normal Russell viper venom assays seen in some cases of congenital factor X deficiency
  • Antonio Girolami
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  • Pamela Scarparo
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American Journal of Hematology (2008) 83 (11): 884.
Congenital FX deficiency combined with other clotting defects or with other abnormalities: a critical evaluation of the literature
  • A. GIROLAMI
  • E. RUZZON
  • F. TEZZA
  • R. SCANDELLARI
  • M. SCAPIN
  • P. SCARPARO
Haemophilia (2008) 14 (2): 323.
Congenital factor X deficiencies with a defect only or predominantly in the extrinsic or in the intrinsic system: A critical evaluation
  • Antonio Girolami
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  • Raffaella Scandellari
  • Emanuele Allemand
American Journal of Hematology (2008) 83 (8): 668.
A New Mutation (Arg251 Trp) in the Ca2+ Binding Site of Factor X Protease Domain Appears to be Responsible for the Defect in the Extrinsic Pathway Activation of Factor X Padua
  • Antonio Girolami
  • Fabrizio Vianello
  • Laura Cabrio
  • Anna Maria Lombardi
Clinical and Applied Thrombosis/Hemostasis (2004) 10 (1): 5.
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 (Lys408→Asn) in the Factor X Gene
  • Paolo Simioni
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  • Michael Kalafatis
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  • Paolo Paolucci
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  • Antonio Girolami
Thrombosis Research (2001) 101 (4): 219.
A New Factor X Defect (Factor X Padua 3)
  • Fabrizio Vianello
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  • Caterina Boldrin
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Thrombosis Research (2001) 104 (4): 257.
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glul02Lys) in the second EGF‐like domain
  • G. MARCHETTI
  • G. CASTAMAN
  • M. PINOTTI
  • B. LUNGHI
  • M. G. DI IASIO
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British Journal of Haematology (1995) 90 (4): 910.
Functional Consequences of the Ser334→Pro Mutation in a Human Factor X Variant (Factor XMarseille)
  • Annie Bezeaud
  • Toshiyuki Miyata
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  • Marie‐Claude Guillin
European Journal of Biochemistry (1995) 234 (1): 140.
A functional factor X deficiency
  • Paul Sun
  • Jane Hata
  • John Bauer
  • Carolyn Haibach
  • Doug Campbell
  • Medhi Farhangi
  • Dan Smith
American Journal of Hematology (1995) 48 (1): 1.
Biochemistry of factor X
  • Mark Hertzberg
Blood Reviews (1994) 8 (1): 56.
The Classification of Congenital Factor X Deficiency and Abnormalities
  • Antonio Girolami
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  • Grazia Ruzza
Annals of Saudi Medicine (1990) 10 (2): 218.
Immunohistochemical localization of factor X-like antigen in pancreatic islets and their tumours
  • Cesare Bordi
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Virchows Archiv A Pathological Anatomy and Histopathology (1990) 416 (5): 397.
Factor × Roma: a congenital factor × variant defective at different degrees in the intrinsic and the extrinsic activation
  • V. De Stefano
  • G. Leone
  • R. Ferrelli
  • H. J. Hassan
  • G. Macioce
  • B. Bizzi
British Journal of Haematology (1988) 69 (3): 387.
Factor × Roma: a congenital factor × variant defective at different degrees in the intrinsic and the extrinsic activation
  • V. De Stefano
  • G. Leone
  • R. Ferrelli
  • H. J. Hassan
  • G. Macioce
  • B. Bizzi
British Journal of Haematology (1988) 69 (3): 387.
Rarer Quantitative and Qualitative Abnormalities of Coagulation
  • A. Girolami
  • L. De Marco
  • R. Dal Bo Zanon
  • G. Patrassi
  • M.G. Cappellato
Clinics in Haematology (1985) 14 (2): 385.
  • Online ISSN 1421-9662
  • Print ISSN 0001-5792
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