Unique skin manifestations of hereditary apolipoprotein A-1 amyloidosis.
作者信息
Moshe-Lilie Orly, Heitner Stephen, Karam Chafic
机构信息
Department of Neurology, Oregon Health & Science University, Neurology, Portland, OR, USA.
Knight Cardiovascular Institute, Oregon Health & Science University, Neurology, Portland, OR, USA.
出版信息
Oxf Med Case Reports. 2020 Mar 30;2020(3):omaa014. doi: 10.1093/omcr/omaa014. eCollection 2020 Mar.
Abstract
摘要
相似文献
1
Unique skin manifestations of hereditary apolipoprotein A-1 amyloidosis.
Oxf Med Case Reports. 2020 Mar 30;2020(3):omaa014. doi: 10.1093/omcr/omaa014. eCollection 2020 Mar.
2
A new genetic variant of hereditary apolipoprotein A-I amyloidosis: a case-report followed by discussion of diagnostic challenges and therapeutic options.遗传性载脂蛋白 A-I 淀粉样变性的一种新遗传变异体：病例报告，并讨论诊断挑战和治疗选择。
BMC Med Genet. 2019 Jan 21;20(1):23. doi: 10.1186/s12881-019-0755-5.
3
Clinical and pathologic characteristics of hereditary apolipoprotein A-I amyloidosis in Ireland.爱尔兰遗传性载脂蛋白 A-I 淀粉样变的临床和病理特征。
Nephrology (Carlton). 2013 Aug;18(8):549-54. doi: 10.1111/nep.12108.
4
[Cardiac manifestations of amyloidosis by deposits of transthyretin and apolipoprotein A1. Report of 3 families].[转甲状腺素蛋白和载脂蛋白A1沉积所致淀粉样变性的心脏表现。3个家族的报告]
Arch Mal Coeur Vaiss. 2003 Jun;96(6):631-5.
5
Primary adrenal insufficiency due to hereditary apolipoprotein AI amyloidosis: endocrine involvement beyond hypogonadism.遗传性载脂蛋白 AI 淀粉样变性所致原发性肾上腺皮质功能减退症：除性腺功能减退症以外的内分泌受累。
Amyloid. 2018 Jun;25(2):75-78. doi: 10.1080/13506129.2018.1438390. Epub 2018 Feb 15.
6
Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis.肾载脂蛋白A-I淀粉样变性：一种罕见且常被忽视的遗传性肾小管间质性肾炎病因。
J Am Soc Nephrol. 2005 Dec;16(12):3680-6. doi: 10.1681/ASN.2005040382. Epub 2005 Oct 12.
7
Two novel APOA1 gene mutations in a Japanese renal transplant recipient with recurrent apolipoprotein A-I related amyloidosis.一名患有复发性载脂蛋白A-I相关性淀粉样变性的日本肾移植受者中发现两种新的APOA1基因突变。
Nephrology (Carlton). 2018 Jul;23 Suppl 2:17-21. doi: 10.1111/nep.13278.
8
Hereditary apolipoprotein AI-associated renal amyloidosis: A diagnostic challenge.遗传性载脂蛋白AI相关性肾淀粉样变性：一项诊断挑战。
Nefrologia. 2015;35(3):322-7. doi: 10.1016/j.nefro.2015.05.002. Epub 2015 Jun 18.
9
A novel apolipoprotein A-1 variant, Arg173Pro, associated with cardiac and cutaneous amyloidosis.一种与心脏和皮肤淀粉样变性相关的新型载脂蛋白A-1变体，即Arg173Pro。
Biochem Biophys Res Commun. 1999 Apr 13;257(2):584-8. doi: 10.1006/bbrc.1999.0518.
10
Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26Arg.肝-肾联合移植治疗载脂蛋白AI Gly26Arg相关遗传性系统性淀粉样变性的临床及生化结局
Transplantation. 2001 Apr 15;71(7):986-92. doi: 10.1097/00007890-200104150-00026.
本文引用的文献
1
A novel apolipoprotein A-1 variant, Arg173Pro, associated with cardiac and cutaneous amyloidosis.一种与心脏和皮肤淀粉样变性相关的新型载脂蛋白A-1变体，即Arg173Pro。
Biochem Biophys Res Commun. 1999 Apr 13;257(2):584-8. doi: 10.1006/bbrc.1999.0518.
Zotero 插件