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Further studies on the abnormal factor X (factor X Friuli) coagulation disorder: a report of another family.

作者信息

Girolami A, Lazzarin M, Scarpa R, Brunetti A

出版信息

Blood. 1971 May;37(5):534-41.

PMID:4995085
Abstract
摘要

相似文献

1
Further studies on the abnormal factor X (factor X Friuli) coagulation disorder: a report of another family.
Blood. 1971 May;37(5):534-41.
2
Another patient with a congenital hemorrhagic disorder intermediate between factor X and factor VII deficiency.另一名患有先天性出血性疾病的患者，其病情介于因子X缺乏和因子VII缺乏之间。
Haematol Lat. 1970 Jan-Mar;13(1):89-102.
3
Further studies on the abnormal factor X (factor X Friuli) coagulation disorder. A report of another family.
Haematol Lat. 1970 Apr-Jun;13(2):169-83.
4
A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): study of a large kindred.
Br J Haematol. 1970 Aug;19(2):179-92. doi: 10.1111/j.1365-2141.1970.tb01615.x.
5
Factor X Friuli coagulation disorder. Report of a newly recognized patient and some considerations on the frequency of the disease in the Friuli area.弗留利X因子凝血障碍。一例新确诊患者的报告及对弗留利地区该病发病率的一些思考。
Acta Haematol. 1976;56(1):27-38. doi: 10.1159/000207916.
6
[Congenital coagulopathy due to the presence of an abnormal factor X (Friuli factor X). A "new" hemorrhagic disease].[因异常X因子（弗留利X因子）存在导致的先天性凝血病。一种“新”的出血性疾病]
Recenti Prog Med. 1970 Oct;49(4):360-84.
7
Abnormal factor X (factor X Friuli) coagulation disorder. The heterozygote population. A study of 57 subjects.
Acta Haematol. 1974;51(1):40-50. doi: 10.1159/000208273.
8
A family with heterozygous factor X Friuli defect outside Friuli.
Blut. 1983 Mar;46(3):149-54. doi: 10.1007/BF00320273.
9
Factor X survival and therapeutic factor X levels in the abnormal factor X (factor X FRIULI) COAGULATION DISORDER.异常凝血因子X（弗留利凝血因子X）凝血障碍中凝血因子X的存活情况及治疗性凝血因子X水平
Acta Haematol. 1974;52(4):223-31. doi: 10.1159/000208245.
10
Abnormal factor X(factor X Friuli) coagulation disorder.异常因子X（弗留利因子X）凝血障碍。
Acta Haematol. 1973;49(2):114-22. doi: 10.1159/000208392.

引用本文的文献

1
Factor X Friuli Coagulation Disorder: Almost 50 Years Later.弗留利X因子凝血障碍：近50年后
Clin Appl Thromb Hemost. 2018 Jan;24(1):33-40. doi: 10.1177/1076029616686423. Epub 2016 Dec 29.
2
Antithrombin III (AT III) Padua2: a "new" congenital abnormality with defective heparin co-factor activities but no thrombotic disease.
Blut. 1983 Aug;47(2):93-103. doi: 10.1007/BF02482643.
3
A new family with classical factor X deficiency as demonstrated by electroimmunoassay.通过免疫电泳法证实的一个患有典型因子X缺乏症的新家族。
Blut. 1983 Jul;47(1):53-7. doi: 10.1007/BF00321050.
4
A family with heterozygous factor X Friuli defect outside Friuli.
Blut. 1983 Mar;46(3):149-54. doi: 10.1007/BF00320273.
5
Factor X level in coumarin treated patients and in factor X deficiency as assayed with different techniques.用不同技术测定的接受香豆素治疗患者及因子X缺乏患者的因子X水平。
Blut. 1972 Aug;25(2):77-84. doi: 10.1007/BF01633871.
6
Molecular deficiencies of human blood coagulation.人类血液凝固的分子缺陷
Experientia. 1972 Jan 15;28(1):1-7. doi: 10.1007/BF01928228.
7
Factor X Friuli coagulation disorder. First report of a patient born in Friuli after the description of the disease.
Blut. 1973 Sep;27(3):151-8. doi: 10.1007/BF01634029.
8
The K-test (trypsin clotting time) in coumarin treated patients and in congenital deficiencies and abnormalities of the prothrombin complex.香豆素治疗患者以及凝血酶原复合物先天性缺陷和异常患者的K试验（胰蛋白酶凝血时间）
Blut. 1975 Nov;31(5):291-8. doi: 10.1007/BF01634145.
9
Factor X Friuli: An immunological study in plasma and in serum using several methods.
Blut. 1975 Mar;30(3):203-12. doi: 10.1007/BF01633955.