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Items: 1 to 20 of 108

1.

A syndrome of ichthyosis, hepatosplenomegaly and cerebellar degeneration.

Dykes PJ, Marks R, Harper PS.

Br J Dermatol. 1979 May;100(5):585-90.

PMID:
444432
2.

Ichthyosis, hepatosplenomegaly, and cerebellar degeneration in a sibship.

Harper PS, Marks R, Dykes PJ, Young ID.

J Med Genet. 1980 Jun;17(3):212-5.

3.

Syndrome of ichthyosis, hepatosplenomegaly and cerebellar degeneration--steroid sulphatase activity.

Dykes PJ, Marks R, Harper PS.

Br J Dermatol. 1980 Mar;102(3):353-4. No abstract available.

PMID:
6445203
4.

[Clinical features and genetics of the ichthyosis vulgaris group].

Traupe H, Happle R.

Fortschr Med. 1980 Dec 11;98(46):1809-15. German.

PMID:
7274918
5.

Ichthyosis-cheek-eyebrow (ICE) syndrome: a new autosomal dominant disorder.

Sidransky E, Feinstein A, Goodman RM.

Clin Genet. 1987 Mar;31(3):137-42.

PMID:
3568439
6.

Autosomal dominant Muckle-Wells syndrome associated with cystinuria, ichthyosis, and aphthosis in a four-generation family.

Berthelot JM, Maugars Y, Robillard N, Pascal O, Stalder JF, David A, Prost A.

Am J Med Genet. 1994 Oct 15;53(1):72-4.

PMID:
7802040
7.

Autosomal dominant lamellar ichthyosis.

Toribio J, Fernández Redondo V, Peteiro C, Zulaica A, Fabeiro JM.

Clin Genet. 1986 Aug;30(2):122-6.

PMID:
3757302
8.

A new syndrome: thrombocytopathia, muscle fatigue, asplenia, miosis, migraine, dyslexia and ichthyosis.

Stormorken H, Sjaastad O, Langslet A, Sulg I, Egge K, Diderichsen J.

Clin Genet. 1985 Nov;28(5):367-74.

PMID:
4085141
9.
10.

Ichthyosis and neutral lipid storage disease.

Musumeci S, D'Agata A, Romano C, Patané R, Cutrona D.

Am J Med Genet. 1988 Feb;29(2):377-82.

PMID:
3354610
11.

A family with late onset autosomal dominant cerebellar degeneration.

Collins S, Sedal L, King J, Donaldson I.

Clin Exp Neurol. 1988;25:61-5.

PMID:
3267486
12.

Ichthyosis. Reliability of clinical signs in the differentiation between autosomal dominant and sex-linked forms.

Bousema M, van Diggelen O, van Joost T, Stolz E, Naafs B.

Int J Dermatol. 1989 May;28(4):240-2.

PMID:
2722337
14.

Possible genetic heterogeneity of X-linked ichthyosis.

Passarge E, Post B, Schöpf E.

Birth Defects Orig Artic Ser. 1971 Jun;7(8):46-9.

PMID:
5173313
15.

[Ichthyosis hystrix with parakeratosis in the form of cornoid lamellae].

Braun-Falco O, Schurig V, Meurer M, Klepzig K.

Hautarzt. 1985 Mar;36(3):132-41. German.

PMID:
4039715
16.

A familial disorder characterized by hepatosplenomegaly presenting as "preleukemia".

Holimon JL, Madge GE.

Va Med Mon (1918). 1971 Dec;98(12):644-8. No abstract available.

PMID:
5129122
17.

[The as yet undescribed regular dominant form of bullous congenital ichthyosiform erythroderma].

Siemens HW.

Hautarzt. 1970 Aug;21(8):352-5. German. No abstract available.

PMID:
5518369
18.

Autosomal dominant lamellar ichthyosis: a new skin disorder.

Traupe H, Kolde G, Happle R.

Clin Genet. 1984 Nov;26(5):457-61.

PMID:
6499258
19.

Congenital ichthyosis, mental retardation, dwarfism and renal impairment: a new syndrome.

Passwell JH, Goodman RM, Ziprkowski M, Cohen BE.

Clin Genet. 1975 Jul;8(1):59-65.

PMID:
1149323
20.

[Collodion baby: 32 new case reports].

Larrègue M, Ottavy N, Bressieux JM, Lorette J.

Ann Dermatol Venereol. 1986;113(9):773-85. Review. French.

PMID:
3548541

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