Literature DB >> 4247927

Inherited ichthyoses.

U W Schnyder.   

Abstract

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Year:  1970        PMID： 4247927

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN： 0003-987X


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  11 in total

1.  Ultrastructure of inborn errors of keratinization. VI. Inherited ichthyoses--a model system for heterogeneities in keratinization disturbances.

Authors:  I Anton-Lamprecht; U W Schnyder
Journal:  Arch Dermatol Forsch       Date:  1974

2.  [Ultrastructure of inborn errors of keratinization. IV. X-linked recessive ichthyosis (author's transl)].

Authors:  I Anton-Lamprecht
Journal:  Arch Dermatol Forsch       Date:  1974-02-20

3.  Sjögren-Larsson syndrome in two sibs with peripheral nerve involvement and bisalbuminaemia.

Authors:  M Maia
Journal:  J Neurol Neurosurg Psychiatry       Date:  1974-12       Impact factor: 10.154

4.  [Ultrastructural study of cutaneous lesions in Jadassohn Lewandowsky syndrome].

Authors:  H Perrot; D Schmitt; J Thivolet
Journal:  Arch Dermatol Forsch       Date:  1973-03-19

5.  Ultrastructural distinction of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosis.

Authors:  I Anton-Lamprecht; M Hofbauer
Journal:  Humangenetik       Date:  1972

6.  Ichthyosis linearis circumflexa Comèl with Trichorrhexis invaginata (Netherton's Syndrom): an ultrastructural study of the skin changes.

Authors:  E Frenk; B Mevorah
Journal:  Arch Dermatol Forsch       Date:  1972

7.  [Ultrastructure of inborn errors of keratinization. 3. Autosomal dominant ichthyosis vulgaris (author's transl)].

Authors:  I Anton-Lamprecht
Journal:  Arch Dermatol Forsch       Date:  1973-12-05

8.  [Ultrastructure of inborn erors of keratinization. I. Ichthyosis congenita].

Authors:  I Anton-Lamprecht
Journal:  Arch Dermatol Forsch       Date:  1972

9.  [Ultrastructure of inborn errors of keratinization. V. Ichthyosis in Refsum's syndrome (heredopathia atactica polyneuritiformis) (author's transl)].

Authors:  I Anton-Lamprecht; W Kahlke
Journal:  Arch Dermatol Forsch       Date:  1974

10.  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.

Authors:  M Münke; K Kruse; M Goos; H H Ropers; M Tolksdorf
Journal:  Eur J Pediatr       Date:  1983-10       Impact factor: 3.183
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