加里-加里病是道林-德戈斯病的一种棘层松解变异型：一个德国家庭的额外遗传学证据。 - Suppr

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超能文献

Galli-Galli disease is an acantholytic variant of Dowling-Degos disease: additional genetic evidence in a German family.

作者信息

Schmieder Astrid, Pasternack Sandra M, Krahl Dieter, Betz Regina C, Leverkus Martin

出版信息

J Am Acad Dermatol. 2012 Jun;66(6):e250-1. doi: 10.1016/j.jaad.2011.07.038.

DOI:10.1016/j.jaad.2011.07.038

PMID:22583733

Abstract

摘要

相似文献

Galli-Galli disease is an acantholytic variant of Dowling-Degos disease: additional genetic evidence in a German family.加里-加里病是道林-德戈斯病的一种棘层松解变异型：一个德国家庭的额外遗传学证据。

J Am Acad Dermatol. 2012 Jun;66(6):e250-1. doi: 10.1016/j.jaad.2011.07.038.

Galli-Galli disease is an acantholytic variant of Dowling-Degos disease.加利-加利病是道林-德戈斯病的一种棘层松解变异型。

Br J Dermatol. 2007 Mar;156(3):572-4. doi: 10.1111/j.1365-2133.2006.07703.x.

Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease.对 KRT5 进行系统突变筛查支持 Galli-Galli 病是 Dowling-Degos 病的一种变体的假说。

Br J Dermatol. 2010 Jul;163(1):197-200. doi: 10.1111/j.1365-2133.2010.09741.x. Epub 2010 Mar 5.

The expanding spectrum of Galli-Galli disease.加利-加利病不断扩大的谱系。

J Am Acad Dermatol. 2007 May;56(5 Suppl):S86-91. doi: 10.1016/j.jaad.2006.10.987.

[Galli-Galli disease. Clinical and histopathological investigation using a case series of 18 patients].[加里-加里病。对18例患者的病例系列进行临床和组织病理学研究]

Hautarzt. 2011 Nov;62(11):842-51. doi: 10.1007/s00105-011-2222-x.

Galli-Galli disease: an unrecognized entity or an acantholytic variant of Dowling-Degos disease?加里-加里病：一种未被认识的疾病实体还是Dowling-Degos病的棘层松解变异型？

J Am Acad Dermatol. 2001 Nov;45(5):760-3. doi: 10.1067/mjd.2001.116340.

[Galli-Galli disease. Review of the literature].

Hautarzt. 2013 Apr;64(4):282. doi: 10.1007/s00105-013-2561-x.

Generalized Dowling-Degos disease.泛发性道林-德戈斯病

J Am Acad Dermatol. 2007 Aug;57(2):327-34. doi: 10.1016/j.jaad.2006.12.023.

[Galli-Galli disease presenting as lichenoid papules in the flexures].[以屈侧苔藓样丘疹为表现的加里-加里病]

Actas Dermosifiliogr. 2010 Mar;101(2):168-72.

Heterozygous frameshift mutation in keratin 5 in a family with Galli-Galli disease.一个患有加里-加里病的家族中角蛋白5的杂合移码突变。

Br J Dermatol. 2014 Jun;170(6):1362-5. doi: 10.1111/bjd.12813.

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Galli-Galli Disease: A Comprehensive Literature Review.加利-加利病：全面的文献综述

Dermatopathology (Basel). 2024 Feb 7;11(1):79-100. doi: 10.3390/dermatopathology11010008.

Exacerbation of Galli-Galli Disease Following Dialysis Treatment: A Case Report and Review of Aggravating Factors.透析治疗后加里-加里病病情加重：一例病例报告及加重因素综述

Cureus. 2021 Jun 2;13(6):e15401. doi: 10.7759/cureus.15401. eCollection 2021 Jun.

Dowling-Degos Disease - A Novel Presentation of An Uncommon Disease.Dowling-Degos病——一种罕见疾病的新表现形式。

Indian Dermatol Online J. 2019 Aug 28;10(5):587-590. doi: 10.4103/idoj.IDOJ_460_18. eCollection 2019 Sep-Oct.

Dew drops on spider web appearance: a newly named pattern of IgG4 deposition in pemphigus with direct immunofluorescence.蜘蛛网样露珠滴外观：一种在天疱疮中通过直接免疫荧光检测到的新命名的IgG4沉积模式。

Postepy Dermatol Alergol. 2017 Aug;34(4):295-298. doi: 10.5114/ada.2017.69306. Epub 2017 Aug 1.

Mutations in POGLUT1 in Galli-Galli/Dowling-Degos disease.加里 - 加里/道林 - 德戈斯病中POGLUT1基因的突变

Br J Dermatol. 2017 Jan;176(1):270-274. doi: 10.1111/bjd.14914. Epub 2016 Sep 24.

Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease.POGLUT1 基因突变导致常染色体显性遗传的 Dowling-Degos 病。

Am J Hum Genet. 2014 Jan 2;94(1):135-43. doi: 10.1016/j.ajhg.2013.12.003.

Heterozygous frameshift mutation in keratin 5 in a family with Galli-Galli disease.一个患有加里-加里病的家族中角蛋白5的杂合移码突变。

Br J Dermatol. 2014 Jun;170(6):1362-5. doi: 10.1111/bjd.12813.

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