[On a case of Thomson's syndrome and epidermolysis bullosa dystrophica-like skin changes].

作者信息

Salamon T, Bogdanović B, Lazović O

出版信息

Arch Klin Exp Dermatol. 1966 Jun 13;225(2):194-206.

PMID:5991617

Abstract

摘要

相似文献

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本文引用的文献

Congenital cutaneous dystrophy (Thomson's type).

Br J Dermatol Syph. 1949 Jun;61(6):197-205. doi: 10.1111/j.1365-2133.1949.tb11084.x.

Essential shrinking of the conjunctiva in a hereditary affection allied to epidermolysis bullosa.

Doc Ophthalmol. 1951;5-6:118-50. doi: 10.1007/BF00143658.

[Association of 3 defects (epidermolysis bullosa. Thomsen's disease and daltonism) in the same family].

Bull Soc Fr Dermatol Syphiligr. 1961 Aug-Oct;68:664-6.

Poikiloderma congenitale in twins; demonstration of patients.

Acta Derm Venereol. 1955;35(1):86-7.

[A SPECIAL FORM OF ECTODERMAL DYSPLASIA WITH HYPOHYDROSIS, HYPOTRICHOSIS, CORNEAL CHANGES, NAIL AND OTHER ANOMALIES IN SIBLINGS].

Arch Klin Exp Dermatol. 1964 Nov 12;220:564-75.

[ON THE CLASSIFICATION, HISTOGENETICS, BLOOD COAGULATION PHYSIOLOGY AND THERAPY OF HEREDITARY EPIDERMOLYSIS].

Arch Klin Exp Dermatol. 1964 May 15;220:38-59.

[IS THERE IN POIKILODERMA ROTHMUND-THOMSON AN AMINOACIDURIA CORRESPONDING TO THE HARTNUP SYNDROME?].

Hautarzt. 1964 Feb;15:91-3.

Poikiloderma congenitale. Report of a case.

Dermatologica. 1962;125:155-60.

[Histological studies on the pathogenesis of epidermolysis bullosa hereditaria].

Arch Klin Exp Dermatol. 1962 Nov 29;215:369-78. doi: 10.1007/BF00693558.

Studies on the pathogenesis of epidermolysis bullosa.

J Invest Dermatol. 1962 Dec;39:551-75. doi: 10.1038/jid.1962.156.

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