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Primary systemic amyloidosis: a review and an experimental, genetic, and clinical study of 29 cases with particular emphasis on the familial form.

作者信息

BLOCK W D, CAREY J G, CURTIS A C, FALLS H F, JACKSON C E, RUKAVINA J G

出版信息

Medicine (Baltimore). 1956 Sep;35(3):239-334.

PMID:13368965
Abstract
摘要

相似文献

1
Primary systemic amyloidosis: a review and an experimental, genetic, and clinical study of 29 cases with particular emphasis on the familial form.原发性系统性淀粉样变性:一项综述及对29例病例的实验、遗传和临床研究,特别关注家族性形式。
Medicine (Baltimore). 1956 Sep;35(3):239-334.
2
[A case of primary systemic amyloidosis].
Klin Med (Mosk). 1958 Feb;36(2):95-101.
3
[Primary systemic amyloidosis (Konigstein-Lubarsch disease)].
Minerva Dermatol. 1959 Mar;34(3):167-73.
4
Primary systemic amyloidosis.
Australas Ann Med. 1957 May;6(2):116-23. doi: 10.1111/imj.1957.6.2.116.
5
Asymptomatic primary systemic amyloidosis.
Ann Intern Med. 1962 Mar;56:397-408. doi: 10.7326/0003-4819-56-3-397.
6
[A case of systemic amyloidosis].
Pol Tyg Lek. 1962 Mar 26;17:488-9.
7
So-called primary systemic amyloidosis probably due to myelomatosis.
Acta Med Scand. 1958 May 6;160(6):431-5. doi: 10.1111/j.0954-6820.1958.tb10367.x.
8
[Primary systemic amyloidosis with diffuse osteomedullary plasmocytosis].
Orv Hetil. 1962 Aug 12;103:1517-9.
9
Primary systemic amyloidosis with cardiac involvement and with Russell bodies in bone marrow.
Ann Intern Med. 1957 Jan;46(1):156-68. doi: 10.7326/0003-4819-46-1-156.
10
Primary familial amyloidosis.
AMA Arch Ophthalmol. 1958 Dec;60(6):1036-43. doi: 10.1001/archopht.1958.00940081056009.

引用本文的文献

1
The plasma disappearance time and catabolic half-life of I-131-labeled normal human gamma globulin in amyloidosis and inrheumatoid arthritis.I-131标记的正常人γ球蛋白在淀粉样变性和类风湿性关节炎中的血浆消失时间及分解代谢半衰期
J Clin Invest. 1961 Oct;40(10):1926-34. doi: 10.1172/JCI104418.
2
THE SITE OF FORMATION AND ULTRASTRUCTURE OF AMYLOID.淀粉样蛋白的形成部位与超微结构
Am J Pathol. 1963 Nov;43(5):837-54.
3
ELECTRON MICROSCOPIC STUDIES OF AMYLOID FIBRILS WITH FERRITINCONJUGATED ANTIBODY.用铁蛋白结合抗体对淀粉样纤维进行的电子显微镜研究。
Am J Pathol. 1963 Oct;43(4):721-38.
4
Biopsy of the rectum as an aid to the diagnosis of amyloidosis.直肠活检辅助淀粉样变性的诊断。
Br Med J. 1962 Feb 10;1(5275):364-7. doi: 10.1136/bmj.1.5275.364.
5
Chronic pseudotumoral edema of the conjunctiva of possible myxedematous and amyloid origin: with report of two cases.可能源于黏液性水肿和淀粉样变性的结膜慢性假瘤样水肿:附两例报告
Trans Am Ophthalmol Soc. 1960;58:132-54.
6
Inheritance of primary systemic amyloidosis.原发性系统性淀粉样变性的遗传方式。
Am J Hum Genet. 1960 Dec;12(4 Pt 1):434-9.
7
Amyloid disease of the bone marrow. Diagnosis by sternal marrow a spiration.骨髓淀粉样变性。通过胸骨骨髓穿刺进行诊断。
Am J Pathol. 1961 Jan;38(1):61-71.
8
Fatal reaction following the intravenous injection of congo red.静脉注射刚果红后的致命反应。
Br Med J. 1957 Jun 15;1(5032):1403. doi: 10.1136/bmj.1.5032.1403.
9
Leptomeningeal amyloid and variant transthyretins.软脑膜淀粉样蛋白和变异型甲状腺素运载蛋白
Am J Pathol. 1996 Feb;148(2):351-4.
10
A transthyretin variant (alanine 49) associated with familial amyloidotic polyneuropathy in a French family.在一个法国家庭中发现的与家族性淀粉样多神经病相关的转甲状腺素蛋白变体(丙氨酸49)
J Med Genet. 1993 Feb;30(2):117-9. doi: 10.1136/jmg.30.2.117.