Further studies on factor VII padua defect: the report of the fourth homozygous patient from the same valley
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine,Hematology
Link
http://link.springer.com/content/pdf/10.1007/BF00319920.pdf
Reference14 articles.
1. Alexander B, Golstein R, Landwehr G, Cook CD (1951) Congenital SPCA deficiency. A hither to unrecognized coagulation defect with hemorrhage rectified by serum and serum fractions. J Clin Invest 30: 237?248
2. Briët E, Loeliger EA, van Tilburg NH, Veltkamp JJ (1976) Molecular variants of factor VII. Thromb Haemost 35: 289?294
3. Denson KWE, Conard J, Samama M (1972) Genetic variants of factor VII. Lancet I: 1234?1234
4. Girolami A, Molaro G, Lazzarin M, Scarpa R, Brunetti A (1970) A new hemorrhagic condition due to the presence of an abnormal factor X (Factor X Friuli). A study of a large kindred. Br J Haematol 19: 179?192
5. Girolami A, Scorza P, Brunetti A, Morgagni C, Santini G (1973) Congenital hypoproconvertinemia (factor VII deficiency). A report of two cases belonging to two different kindreds. Acta Haematol 50: 228?237
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1. Diagnosis of FVII Padua (Arg304Gln) by means of simple clotting tests;Clinica Chimica Acta;2010-12
2. Ox Brain versus Rabbit Brain Thromboplastin Assays Are the Best Tool for a Preliminary Diagnosis of the Arg304Gln Factor VII Defect (FVII Padua);Acta Haematologica;2010
3. The spectrum of factor VII deficiencies and abnormalities;Blood Coagulation & Fibrinolysis;2004-04
4. Andere angeborene Koagulopathien;Blut und Blutkrankheiten;1985
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