A ‘New’ Congenital Haemorrhagic Condition due to the Presence of an Abnormal Factor X (Factor X Friuli): Study of a Large Kindred
- 1 August 1970
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 19 (2), 179-192
- https://doi.org/10.1111/j.1365-2141.1970.tb01615.x
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Congenital Haemorrhagic Condition Similar but Not Identical to Factor X DeficiencyScandinavian Journal of Haematology, 1970
- An investigation of three patients with Christmas disease due to an abnormal type of factor ixJournal of Clinical Pathology, 1968
- A New Inherited Coagulation Disorder Caused by an Abnormal Fibrinogen (‘Fibrinogen Baltimore’)Nature, 1965
- THE INHERITANCE OF STUART DISEASEThe American Journal of the Medical Sciences, 1965
- The Specific Assay of Prower-Stuart Factor and Factor VIIActa Haematologica, 1961
- The Stuart-Prower Factor: Utilization of Clotting Factors obtained by Starch-Block Electrophoresis for Genetic EvaluationBritish Journal of Haematology, 1961
- A Rapid Screening Test for Disorders of Thromboplastin GenerationBritish Journal of Haematology, 1957
- Stuart Clotting Defect. I. Segregation of an Hereditary Hemorrhagic State from the Heterogeneous Group Heretofore Called “Stable Factor” (SPCA, Proconvertin, Factor VII) DeficiencyJCI Insight, 1957
- Stuart Clotting Defect. II. Genetic Aspects of a `New' Hemorrhagic StateJCI Insight, 1957
- A ‘New’ Coagulation DefectBritish Journal of Haematology, 1956