Brandrup F - Search Results

1

A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.

Betz RC, Lee YA, Bygum A, Brandrup F, Bernal AI, Toribio J, Alvarez JI, Kukuk GM, Ibsen HH, Rasmussen HB, Wienker TF, Reis A, Propping P, Kruse R, Cichon S, Nöthen MM. Betz RC, et al. Among authors: brandrup f. Am J Hum Genet. 2000 Jun;66(6):1979-83. doi: 10.1086/302934. Epub 2000 May 2. Am J Hum Genet. 2000. PMID: 10793007 Free PMC article.

2

Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.

Ibsen HH, Clemmensen OJ, Brandrup F. Ibsen HH, et al. Among authors: brandrup f. Acta Derm Venereol. 1991;71(4):349-51. Acta Derm Venereol. 1991. PMID: 1681656

3

A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype association.

Melin M, Klar J, Jr Gedde-Dahl T, Fredriksson R, Hausser I, Brandrup F, Bygum A, Vahlquist A, Hellström Pigg M, Dahl N. Melin M, et al. Among authors: brandrup f. J Hum Genet. 2006;51(10):864-871. doi: 10.1007/s10038-006-0035-z. Epub 2006 Sep 1. J Hum Genet. 2006. PMID: 16946994

4

Identification of two new mutations in the TAT gene in a Danish family with tyrosinaemia type II.

Pasternack SM, Betz RC, Brandrup F, Gade EF, Clemmensen O, Lund AM, Christensen E, Bygum A. Pasternack SM, et al. Among authors: brandrup f. Br J Dermatol. 2009 Mar;160(3):704-6. doi: 10.1111/j.1365-2133.2008.08888.x. Epub 2008 Oct 13. Br J Dermatol. 2009. PMID: 18945316 No abstract available.

5

Association between CYP1A2 polymorphism and susceptibility to porphyria cutanea tarda.

Christiansen L, Bygum A, Jensen A, Thomsen K, Brandrup F, Hørder M, Petersen NE. Christiansen L, et al. Among authors: brandrup f. Hum Genet. 2000 Dec;107(6):612-4. doi: 10.1007/s004390000415. Hum Genet. 2000. PMID: 11153915

6

[Giant cell arteritis and scalp necrosis].

Bygum A, Brandrup F. Bygum A, et al. Among authors: brandrup f. Ugeskr Laeger. 2000 May 1;162(18):2566-7. Ugeskr Laeger. 2000. PMID: 10846957 Danish.

7

Correction of steroid sulfatase deficiency by gene transfer into basal cells of tissue-cultured epidermis from patients with recessive X-linked ichthyosis.

Jensen TG, Jensen UB, Jensen PK, Ibsen HH, Brandrup F, Ballabio A, Bolund L. Jensen TG, et al. Among authors: brandrup f. Exp Cell Res. 1993 Dec;209(2):392-7. doi: 10.1006/excr.1993.1326. Exp Cell Res. 1993. PMID: 8262159

8

Steroid sulphatase deficiency disease.

Lykkesfeldt G, Høyer H, Ibsen HH, Brandrup F. Lykkesfeldt G, et al. Among authors: brandrup f. Clin Genet. 1985 Sep;28(3):231-7. doi: 10.1111/j.1399-0004.1985.tb00391.x. Clin Genet. 1985. PMID: 2866054

9

Tinea corporis due to Trichophyton verrucosum in recessive, X-linked ichthyosis.

Ibsen HH, Brandrup F. Ibsen HH, et al. Among authors: brandrup f. Mycoses. 1993 Sep-Oct;36(9-10):319-20. doi: 10.1111/j.1439-0507.1993.tb00774.x. Mycoses. 1993. PMID: 8015564

10

Iron overload in porphyria cutanea tarda.

Bygum A, Brandrup F. Bygum A, et al. Among authors: brandrup f. Br J Dermatol. 2000 Nov;143(5):1116. doi: 10.1046/j.1365-2133.2000.03874.x. Br J Dermatol. 2000. PMID: 11069545 No abstract available.

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