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HEREDITARY DEFICIENCIES OF CLOTTING FACTORS VII AND X ASSOCIATED WITH CAROTID-BODY TUMORS.

作者信息

KROLL A J, ALEXANDER B, COCHIOS F, PECHET L

出版信息

N Engl J Med. 1964 Jan 2;270:6-13. doi: 10.1056/NEJM196401022700102.

DOI:10.1056/NEJM196401022700102
PMID:14062129
Abstract
摘要

相似文献

1
HEREDITARY DEFICIENCIES OF CLOTTING FACTORS VII AND X ASSOCIATED WITH CAROTID-BODY TUMORS.与颈动脉体瘤相关的凝血因子VII和X遗传性缺乏症。
N Engl J Med. 1964 Jan 2;270:6-13. doi: 10.1056/NEJM196401022700102.
2
Congenital bleeding disorders of the vitamin K-dependent clotting factors.维生素K依赖凝血因子的先天性出血性疾病。
Vitam Horm. 2008;78:281-374. doi: 10.1016/S0083-6729(07)00014-3.
3
[Proceedings: Congenital deficiencies of factors II, V, VII and X].[会议论文：凝血因子II、V、VII和X先天性缺乏症]
Minerva Pediatr. 1973 Dec 15;25(43):1933-42.
4
[A new case of homozygous congenital factor VII deficiency. Associated factor X deficiency in some members of the family].
Ann Pediatr (Paris). 1971 Dec 14;18(12):817-23.
5
Hypoprothrombinemia and hypoproconvertinemia during pregnancy.妊娠期低凝血酶原血症和低凝血因子转化素血症。
J Lab Clin Med. 1955 Feb;45(2):308-12.
6
[ACQUIRED HEMORRHAGIC DIATHESIS CAUSED BY DEFECT OF FACTORS II, VII AND X].[因凝血因子II、VII和X缺乏导致的获得性出血素质]
Hemostase. 1963 Apr-Jun;3:111-7.
7
[Artificial hypoprothrombinemia and hypoproconvertinemia as liver function tests].[人工诱导低凝血酶原血症和低凝血酶原转变加速因子血症作为肝功能试验]
Prensa Med Argent. 1953 Aug 7;40(32):2102-6.
8
BEHAVIOUR OF FACTORS II, VII, IX AND X IN BLEEDING COMPLICATIONS DURING LONG-TERM TREATMENT WITH COUMARIN.香豆素长期治疗期间出血并发症中凝血因子II、VII、IX和X的行为
Thromb Diath Haemorrh. 1964 Jan 1;10:278-81.
9
EXCHANGE TRANSFUSION IN HEREDITARY FACTOR VII (PROCONVERTIN) DEFICIENCY.
Am J Clin Pathol. 1965 Aug;44:198-202. doi: 10.1093/ajcp/44.2.198.
10
Transfusion support for congenital clotting deficiencies other than haemophilia.除血友病外的先天性凝血缺陷的输血支持
Clin Haematol. 1984 Feb;13(1):119-35.

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SDH-related pheochromocytoma and paraganglioma.与 SDH 相关的嗜铬细胞瘤和副神经节瘤。
Best Pract Res Clin Endocrinol Metab. 2010 Jun;24(3):415-24. doi: 10.1016/j.beem.2010.04.001.
2
Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.11号染色体q23区域上家族性非嗜铬性副神经节瘤印记基因的精细定位
Am J Hum Genet. 1997 Jan;60(1):121-32.
3
Studies on a family with combined functional deficiencies of vitamin K-dependent coagulation factors.维生素K依赖凝血因子联合功能缺陷的一个家族的研究
J Clin Invest. 1982 Jun;69(6):1253-60. doi: 10.1172/jci110564.
4
Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34).凝血因子VII和X缺乏与13号染色体（q34）缺失相关。来自两例核型为46,XY,t(13;Y)(q11;q34)病例的证据。
Hum Genet. 1982;62(4):358-60. doi: 10.1007/BF00304557.
5
Genetic aspects of nonchromaffin paraganglioma.非嗜铬性副神经节瘤的遗传学方面
Hum Genet. 1982;60(4):305-9. doi: 10.1007/BF00569208.
6
[On the treatment of Factor II, VII and X deficiency with P.P.S.B].
Blut. 1968 Jan;16(4):220-4. doi: 10.1007/BF01631671.
7
Bilateral familial carotid body tumors: report of a patient with an occult contralateral tumor and postoperative hypertension.双侧家族性颈动脉体瘤：1例隐匿性对侧肿瘤及术后高血压患者的报告
Ann Surg. 1971 Aug;174(2):242-7. doi: 10.1097/00000658-197108000-00011.
8
Carotid body tumors. Familial and bilateral.颈动脉体瘤。家族性及双侧性。
Ann Surg. 1970 Jun;171(6):843-8. doi: 10.1097/00000658-197006010-00004.
9
Genetics of human blood coagulation.人类血液凝固的遗传学
J Med Genet. 1965 Dec;2(4):254-303. doi: 10.1136/jmg.2.4.254.
10
Production and characterization of a human monoclonal antibody recognizing a new antigen expressed on some lymphoid cells.一种识别某些淋巴细胞上表达的新抗原的人单克隆抗体的制备与特性分析
Jpn J Cancer Res. 1990 Feb;81(2):153-60. doi: 10.1111/j.1349-7006.1990.tb02542.x.