Küster W - Search Results

1

A family study of atopic dermatitis. Clinical and genetic characteristics of 188 patients and 2,151 family members.

Küster W, Petersen M, Christophers E, Goos M, Sterry W. Küster W, et al. Arch Dermatol Res. 1990;282(2):98-102. doi: 10.1007/BF00493466. Arch Dermatol Res. 1990. PMID: 2353830

2

Cytogenetic effects during extracorporeal photopheresis treatment of two patients with cutaneous T-cell lymphoma.

Peterseim UM, Küster W, Gebauer HJ, Meschig R, Plewig G. Peterseim UM, et al. Among authors: kuster w. Arch Dermatol Res. 1991;283(2):81-5. doi: 10.1007/BF00371613. Arch Dermatol Res. 1991. PMID: 2069416

3

The genetics of Crohn disease: complex segregation analysis of a family study with 265 patients with Crohn disease and 5,387 relatives.

Küster W, Pascoe L, Purrmann J, Funk S, Majewski F. Küster W, et al. Am J Med Genet. 1989 Jan;32(1):105-8. doi: 10.1002/ajmg.1320320122. Am J Med Genet. 1989. PMID: 2705471

4

A major susceptibility locus for atopic dermatitis maps to chromosome 3q21.

Lee YA, Wahn U, Kehrt R, Tarani L, Businco L, Gustafsson D, Andersson F, Oranje AP, Wolkertstorfer A, v Berg A, Hoffmann U, Küster W, Wienker T, Rüschendorf F, Reis A. Lee YA, et al. Among authors: kuster w. Nat Genet. 2000 Dec;26(4):470-3. doi: 10.1038/82625. Nat Genet. 2000. PMID: 11101848

5

German adaptation of the Skindex-29 questionnaire on quality of life in dermatology: validation and clinical results.

Augustin M, Wenninger K, Amon U, Schroth MJ, Küster W, Chren M, Kupfer J, Gieler U. Augustin M, et al. Among authors: kuster w. Dermatology. 2004;209(1):14-20. doi: 10.1159/000078581. Dermatology. 2004. PMID: 15237262

6

Progressive erythrokeratodermia and cochlear hearing impairment. A case report and review of the literature.

Lamprecht A, Goecke T, Anton-Lamprecht I, Küster W. Lamprecht A, et al. Among authors: kuster w. Int J Pediatr Otorhinolaryngol. 1988 Sep;15(3):279-89. doi: 10.1016/0165-5876(88)90083-3. Int J Pediatr Otorhinolaryngol. 1988. PMID: 2973446 Review.

7

Indication for the identity of palmoplantar keratoderma type Unna-Thost with type Vörner. Thost's family revisited 110 years later.

Küster W, Becker A. Küster W, et al. Acta Derm Venereol. 1992;72(2):120-2. Acta Derm Venereol. 1992. PMID: 1350396

8

The CHILD nevus: a distinct skin disorder.

Happle R, Mittag H, Küster W. Happle R, et al. Among authors: kuster w. Dermatology. 1995;191(3):210-6. doi: 10.1159/000246548. Dermatology. 1995. PMID: 8534939 Review.

9

Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiency.

Jonkman MF, de Jong MC, Heeres K, Steijlen PM, Owaribe K, Küster W, Meurer M, Gedde-Dahl T Jr, Sonnenberg A, Bruckner-Tuderman L. Jonkman MF, et al. Among authors: kuster w. Arch Dermatol. 1996 Feb;132(2):145-50. doi: 10.1001/archderm.132.2.145. Arch Dermatol. 1996. PMID: 8629821 Free article.

10

[Schöpf syndrome. Clinical, genetic and lipid biochemical studies].

Küster W, Hammerstein W. Küster W, et al. Hautarzt. 1992 Dec;43(12):763-6. Hautarzt. 1992. PMID: 1473970 German.

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