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An electron microscopic study of epidermolytic hyperkeratosis. With a special note on the keratinosome as the "fourth" structural factor in the formation of the horny layer.

作者信息

Wilgram G F, Caulfield J B

出版信息

Arch Dermatol. 1966 Aug;94(2):127-43. doi: 10.1001/archderm.94.2.127.

DOI:10.1001/archderm.94.2.127
PMID:5911501
Abstract
摘要

相似文献

1
An electron microscopic study of epidermolytic hyperkeratosis. With a special note on the keratinosome as the "fourth" structural factor in the formation of the horny layer.表皮松解性角化过度的电子显微镜研究。特别关注角质小体作为角质层形成中的“第四”结构因素。
Arch Dermatol. 1966 Aug;94(2):127-43. doi: 10.1001/archderm.94.2.127.
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[Bullous ichthyosis. A particular form of epidermolytic hyperkeratosis].[大疱性鱼鳞病。表皮松解性角化过度的一种特殊形式]
Med Cutan Ibero Lat Am. 1989;17(6):379-82.
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Ichthyosis bullosa of Siemens: a unique type of epidermolytic hyperkeratosis.西门斯大疱性鱼鳞病：一种独特类型的表皮松解性角化过度症。
J Am Acad Dermatol. 1986 Jun;14(6):1000-5. doi: 10.1016/s0190-9622(86)70123-0.
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Keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK-syndrome): a rare, autosomal recessive disorder of keratohyaline formation?先天性鱼鳞病和硬化性角皮病伴线状角化病（KLICK综合征）：一种罕见的常染色体隐性遗传性透明角质形成障碍疾病？
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Ichthyosis hystrix (Curth-Macklin). Light and electron microscopic studies performed before and after etretinate treatment.
Arch Dermatol. 1984 Sep;120(9):1218-23. doi: 10.1001/archderm.120.9.1218.
6
[Physiopathology of keratogenesis--electron microscopy study].[角膜生成的病理生理学——电子显微镜研究]
Nihon Ishikai Zasshi. 1969 Feb;61(3):375-90.
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[Familial palmo-plantar keratoderma with epidermolytic hyperkeratosis (author's transl)].伴表皮松解性角化过度的家族性掌跖角化病（作者译）
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Ichthyosis with laminated membrane structures.伴有层状膜结构的鱼鳞病
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A particular subtype of ichthyosis congenita type III. Clinical, light, and electron microscopic features.
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s-HBEGF/SIRT1 circuit-dictated crosstalk between vascular endothelial cells and keratinocytes mediates sorafenib-induced hand-foot skin reaction that can be reversed by nicotinamide.s-HBEGF/SIRT1 通路调控的血管内皮细胞与角质形成细胞间相互作用介导索拉非尼致手足皮肤不良反应，烟酰胺可逆转该不良反应。
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Epidermolytic hyperkeratosis: clinical update.表皮松解性角化过度：临床进展
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Ichthyosis update: towards a function-driven model of pathogenesis of the disorders of cornification and the role of corneocyte proteins in these disorders.
鱼鳞病最新进展：迈向角质化障碍发病机制的功能驱动模型以及角质形成细胞蛋白在这些疾病中的作用
Adv Dermatol. 2007;23:231-56. doi: 10.1016/j.yadr.2007.07.011.
4
Genetic mutations in the K1 and K10 genes of patients with epidermolytic hyperkeratosis. Correlation between location and disease severity.表皮松解性角化过度症患者K1和K10基因的基因突变。位置与疾病严重程度之间的相关性。
J Clin Invest. 1994 Apr;93(4):1533-42. doi: 10.1172/JCI117132.
5
An ultrastructural study of epidermolytic leukoplakia.
Arch Dermatol Res. 1983;275(2):86-91. doi: 10.1007/BF00412880.
6
[Erythrodermia ichthyosiformis congenita bullosa brocq. on the so-called granular degeneration. I. Introduction and report of cases].[先天性大疱性鱼鳞病样红皮病（布罗克型）的所谓颗粒变性。I. 病例介绍与报告]
Arch Klin Exp Dermatol. 1968 May 9;231(4):424-36.
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[Odland bodies (Membrane coating granules, keratinosomes) as epidermal lysosomes. An electron microscopic-cytochemical contribution on the cornification process of the skin].[奥兰德小体（膜被颗粒、角蛋白小体）作为表皮溶酶体。关于皮肤角化过程的电子显微镜细胞化学研究]
Arch Klin Exp Dermatol. 1967;231(1):1-19.
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A case of biphasic ichthyosiform dermatosis: light and electron microscopic study.
Arch Klin Exp Dermatol. 1970;237(3):737-48. doi: 10.1007/BF00518496.
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[Ultrastructure of inborn erors of keratinization. I. Ichthyosis congenita].[角化先天性缺陷的超微结构。I. 先天性鱼鳞病]
Arch Dermatol Forsch. 1972;243(2):88-100.
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The ultrastructure of binucleate keratinocytes and binucleation in palatal mucosa of guinea pigs.豚鼠腭黏膜中双核角质形成细胞的超微结构及双核化
Cell Tissue Res. 1974 Jul 3;150(1):113-23. doi: 10.1007/BF00220385.