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Classical Factor X Deficiency: Report of a Further Case

Acta Haematol (1975) 53 (2): 118–127.

This article has been cited by the following articles in journals that are participating in CrossRef Cited-by Linking.

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)

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European Journal of Haematology (2016) 97 (6): 547.

A rare cause of intracranial hemorrhage: Factor X deficiency

AGOP ÇITAK
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Detection of the carrier state in congenital “true” prothrombin deficiency

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American Journal of Hematology (1988) 27 (4): 306.

Factor X antigen evaluation by means of a laser nephelometer in health and disease

A. Girolami
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A family with heterozygous factor X friuli defect outside friuli

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A new family with classical factor X deficiency as demonstrated by electroimmunoassay

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Inherited factor X deficiency: Presentation of a case with etiologic and treatment considerations

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Oral Surgery, Oral Medicine, Oral Pathology (1983) 56 (5): 461.

Immunohistochemical identification of factor X-like antigen in the A cells of the normal human pancreas

C. Betterle
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Incidence, significance, and subtypes of hemophilia BM in a large population of hemophilia B patients

A. Girolami
R. Bo Zanon
P. Saltarin
V. Quaino
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T. Ripa
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Blut (1982) 44 (1): 41.

Hemophilia B with associated factor VII deficiency: A distinct variant of hemophilia B with low factor VII activity and normal factor VII antigen

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