124 related articles for article (PubMed ID: 4119872)
1. [Dry congenital erythroderma ichthyosiforme, deaf-mutism, and hypetomegaly, of recessive autosome transmission. Study of a family].
Desmons F; Bar J; Chevillard Y
Bull Soc Fr Dermatol Syphiligr; 1971; 78(6):585-91. PubMed ID: 4119872
[No Abstract] [Full Text] [Related]
2. [Clinical features and genetics of the ichthyosis vulgaris group].
Traupe H; Happle R
Fortschr Med; 1980 Dec; 98(46):1809-15. PubMed ID: 7274918
[TBL] [Abstract][Full Text] [Related]
3. [A rare oculo-auriculo-cutaneous syndrome (Burns' syndrome)].
Legrand J; Litoux P; Quere M; Stalder JF; Ertus M
J Fr Ophtalmol; 1982; 5(6-7):441-5. PubMed ID: 7130633
[No Abstract] [Full Text] [Related]
4. [Ichthyosis vulgaris, deafness, pili torti and tooth abnormalities].
Braun-Falco O; Landthaler M
Hautarzt; 1978 May; 29(5):276-80. PubMed ID: 659109
[TBL] [Abstract][Full Text] [Related]
5. Ichthyosis and neutral lipid storage disease.
Williams ML; Koch TK; O'Donnell JJ; Frost PH; Epstein LB; Grizzard WS; Epstein CJ
Am J Med Genet; 1985 Apr; 20(4):711-26. PubMed ID: 3993689
[TBL] [Abstract][Full Text] [Related]
6. [Keratotic neurocutaneous syndromes].
Tercedor J; García A
Rev Neurol; 1997 Sep; 25 Suppl 3():S238-42. PubMed ID: 9273168
[TBL] [Abstract][Full Text] [Related]
7. [Differentiation signs of X-chromosomal recessive and autosome dominant ichthyosis vulgaris].
Woźniak L; Omulecki A
Dermatol Monatsschr; 1970; 156(5):503-13. PubMed ID: 4102610
[No Abstract] [Full Text] [Related]
8. Alopecia ichthyotica. A characteristic feature of congenital ichthyosis.
Traupe H; Happle R
Dermatologica; 1983; 167(5):225-30. PubMed ID: 6653846
[TBL] [Abstract][Full Text] [Related]
9. [Mode of inheritance of congenital deaf-mutism].
Hu DN; Qiu WQ; Wu BT; Fang LZ; Zhou F; Gu YP; Zhang QH; Yan JH
Yi Chuan Xue Bao; 1988; 15(4):303-8. PubMed ID: 3273676
[No Abstract] [Full Text] [Related]
10. Diffuse hyperkeratosis in a deaf and blind 48-year-old woman--quiz case. Diagnosis: keratitis-ichthyosis-deafness (KID) syndrome with secondary dermatophytosis.
Machan M; Kestenbaum T; Fraga GR
Arch Dermatol; 2012 Oct; 148(10):1199-200. PubMed ID: 23069961
[No Abstract] [Full Text] [Related]
11. Keratitis-ichthyosis-deafness (KID) syndrome with squamous cell carcinoma.
Conrado LA; Marques SA; Lastoria JC; Cucé LC; Marques ME; Dillon NL
Int J Dermatol; 2007 Apr; 46(4):403-6. PubMed ID: 17442084
[No Abstract] [Full Text] [Related]
12. Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas.
Grob JJ; Breton A; Bonafe JL; Sauvan-Ferdani M; Bonerandi JJ
Arch Dermatol; 1987 Jun; 123(6):777-82. PubMed ID: 3579358
[TBL] [Abstract][Full Text] [Related]
13. [What happened to Brocq's types of erythroderma congenitalis ichthyosiformis?].
Schnyder UW
Hautarzt; 1986 Mar; 37(3):123-5. PubMed ID: 3700099
[TBL] [Abstract][Full Text] [Related]
14. Auditory manifestations of Keratitis-Ichthyosis-Deafness (KID) syndrome.
Szymko-Bennett YM; Russell LJ; Bale SJ; Griffith AJ
Laryngoscope; 2002 Feb; 112(2):272-80. PubMed ID: 11889383
[TBL] [Abstract][Full Text] [Related]
15. The pattern of inheritance in KID syndrome.
Restano L; Cambiaghi S; Tadini G
Pediatr Dermatol; 1999; 16(2):164-5. PubMed ID: 10337688
[No Abstract] [Full Text] [Related]
16. Elevated n-alkanes in congenital ichthyosiform erythroderma. Phenotypic differentiation of two types of autosomal recessive ichthyosis.
Williams ML; Elias PM
J Clin Invest; 1984 Jul; 74(1):296-300. PubMed ID: 6736251
[TBL] [Abstract][Full Text] [Related]
17. Ichthyoses: differential diagnosis and molecular genetics.
Oji V; Traupe H
Eur J Dermatol; 2006; 16(4):349-59. PubMed ID: 16935789
[TBL] [Abstract][Full Text] [Related]
18. [Bullous form of Brocq's congenital erythroderma ichthyosiforme].
Plechistova LA; Rasulev AKh
Vestn Dermatol Venerol; 1989; (4):70-2. PubMed ID: 2669412
[TBL] [Abstract][Full Text] [Related]
19. [Ultrastructural distinctive features of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosis].
Anton-Lamprecht I; Hofbauer M
Dermatologica; 1972; 145(1):60-4. PubMed ID: 4658662
[No Abstract] [Full Text] [Related]
20. Hereditary syndromes with auditory and dermatological manifestations.
Reed WB; Stone VM; Boder E; Ziprkowski L
Arch Dermatol; 1967 May; 95(5):456-61. PubMed ID: 4164668
[No Abstract] [Full Text] [Related]
[Next] [New Search]
