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Inherited ichthyoses.

作者信息

Schnyder U W

出版信息

Arch Dermatol. 1970 Sep;102(3):240-52.

PMID:4247927
Abstract
摘要

相似文献

1
Inherited ichthyoses.遗传性鱼鳞病
Arch Dermatol. 1970 Sep;102(3):240-52.
2
Ichthyosis vulgaris palmaris et plantaris dominans: a peculiar form of ichthyosis vulgaris localized on the palms and soles.
Dermatologica. 1982;165(6):627-35.
3
[Unusual histologic image of some systematized verrucous naevi].[某些系统性疣状痣的不寻常组织学图像]
Ann Dermatol Syphiligr (Paris). 1969;96(4):361-74.
4
[Monstruous familial palmo-plantar hyperkeratosis with pigmented ichthyosiform keratosis of the chest and back, observed in the Malagasy Republic. Nosographical discussion].
Bull Soc Fr Dermatol Syphiligr. 1970;77(2):232-4.
5
[Acromelic hyperkeratotic dermatosis associated with cancer of the palatal velum (Bazex disease)].[与腭帆癌相关的肢端角化过度性皮肤病（巴泽克斯病）]
Bull Soc Fr Dermatol Syphiligr. 1967;74(4):516-20.
6
[Ultrastructural distinctive features of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosis].
Dermatologica. 1972;145(1):60-4.
7
Palmoplantar keratosis acuminata with facial sebaceous hyperplasia.掌跖尖状角化病伴面部皮脂腺增生。
Arch Dermatol. 1974 Jan;109(1):86-7.
8
[Hematoderma in an adult with cutaneous eruption of the Letterer-Siwe type. Nosologic discussion].[成人Letterer-Siwe型皮肤疹伴发的血液病性皮病。病种学讨论]
Bull Soc Fr Dermatol Syphiligr. 1969;76(5):729.
9
The prevalence of accentuated palmoplantar markings and keratosis pilaris in atopic dermatitis, autosomal dominant ichthyosis and control dermatological patients.特应性皮炎、常染色体显性鱼鳞病及对照皮肤科患者中掌跖纹加深和毛发角化病的患病率。
Br J Dermatol. 1985 Jun;112(6):679-85. doi: 10.1111/j.1365-2133.1985.tb02336.x.
10
[Differentiation signs of X-chromosomal recessive and autosome dominant ichthyosis vulgaris].
Dermatol Monatsschr. 1970;156(5):503-13.

引用本文的文献

1
Epidermolytic hyperkeratosis: clinical update.表皮松解性角化过度：临床进展
Clin Cosmet Investig Dermatol. 2019 May 8;12:333-344. doi: 10.2147/CCID.S166849. eCollection 2019.
2
Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome. Clinical and biochemical investigations on two patients with Rud syndrome and review of the literature.鱼鳞病、性腺功能减退、智力发育迟缓及癫痫综合征的遗传异质性。对两名Rud综合征患者的临床及生化研究并文献复习。
Eur J Pediatr. 1983 Oct;141(1):8-13. doi: 10.1007/BF00445661.
3
[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.
4
[Ultrastructure of inborn errors of keratinization. 3. Autosomal dominant ichthyosis vulgaris (author's transl)].[角化先天性缺陷的超微结构。3. 常染色体显性寻常型鱼鳞病（作者译）]
Arch Dermatol Forsch. 1973 Dec 5;248(2):149-72.
5
Ichthyosis linearis circumflexa Comèl with Trichorrhexis invaginata (Netherton's Syndrom): an ultrastructural study of the skin changes.
Arch Dermatol Forsch. 1972;245(1):42-9. doi: 10.1007/BF00596151.
6
Ultrastructure of inborn errors of keratinization. VI. Inherited ichthyoses--a model system for heterogeneities in keratinization disturbances.角化先天性缺陷的超微结构。VI. 遗传性鱼鳞病——角化紊乱异质性的模型系统。
Arch Dermatol Forsch. 1974;250(3):207-27.
7
Sjögren-Larsson syndrome in two sibs with peripheral nerve involvement and bisalbuminaemia.两例伴有周围神经受累和双白蛋白血症的同胞患舍格伦-拉尔松综合征。
J Neurol Neurosurg Psychiatry. 1974 Dec;37(12):1306-15. doi: 10.1136/jnnp.37.12.1306.
8
[Ultrastructure of inborn errors of keratinization. IV. X-linked recessive ichthyosis (author's transl)].[角化先天性缺陷的超微结构。IV. X连锁隐性鱼鳞病（作者译）]
Arch Dermatol Forsch. 1974 Feb 20;248(4):361-78.
9
[Ultrastructure of inborn errors of keratinization. V. Ichthyosis in Refsum's syndrome (heredopathia atactica polyneuritiformis) (author's transl)].[角化先天性缺陷的超微结构。V. 雷夫叙姆综合征（多神经炎型遗传性共济失调）中的鱼鳞病（作者译）]
Arch Dermatol Forsch. 1974;250(3):185-206.
10
[Ultrastructural study of cutaneous lesions in Jadassohn Lewandowsky syndrome].[雅-莱综合征皮肤损害的超微结构研究]
Arch Dermatol Forsch. 1973 Mar 19;246(2):114-24. doi: 10.1007/BF00595528.