König A - Search Results

1

Guess what! X-linked dominant chondrodysplasia punctata (Conradi-Hünermann-Happle Syndrome).

Krisp A, König A, Hoffmann R, Happle R. Krisp A, et al. Among authors: konig a. Eur J Dermatol. 2001 Jul-Aug;11(4):389-91. Eur J Dermatol. 2001. PMID: 11458930 No abstract available.

2

Vulvar amyloidosis mimicking giant condylomata acuminata in a patient with multiple myeloma.

Konig A, Wennemuth G, Soyer HP, Hoffmann R, Happle R, Krause W. Konig A, et al. Eur J Dermatol. 1999 Jan-Feb;9(1):29-31. Eur J Dermatol. 1999. PMID: 9920983

3

Two cases of type 2 segmental manifestation in a family with cutaneous leiomyomatosis.

König A, Happle R. König A, et al. Eur J Dermatol. 2000 Dec;10(8):590-2. Eur J Dermatol. 2000. PMID: 11125318

4

Hermansky-Pudlak syndrome.

Krisp A, Hoffman R, Happle R, König A, Freyschmidt-Paul P. Krisp A, et al. Among authors: konig a. Eur J Dermatol. 2001 Jul-Aug;11(4):372-3. Eur J Dermatol. 2001. PMID: 11399548

5

IFN-gamma-induced HLA-DR but not ICAM-1 expression on cultured dermal papilla cells is downregulated by TNF-alpha.

König A, Happle R, Hoffmann R. König A, et al. Arch Dermatol Res. 1997 Jul;289(8):466-70. doi: 10.1007/s004030050222. Arch Dermatol Res. 1997. PMID: 9266024

6

Type 2 segmental manifestation of multiple glomus tumors: A review and reclassification of 5 case reports.

Happle R, König A. Happle R, et al. Among authors: konig a. Dermatology. 1999;198(3):270-2. doi: 10.1159/000018128. Dermatology. 1999. PMID: 10393451 Review.

7

Linear lesions reflecting lyonization in women heterozygous for IFAP syndrome (ichthyosis follicularis with atrichia and photophobia).

König A, Happle R. König A, et al. Am J Med Genet. 1999 Aug 6;85(4):365-8. doi: 10.1002/(sici)1096-8628(19990806)85:4<365::aid-ajmg12>3.0.co;2-#. Am J Med Genet. 1999. PMID: 10398262

8

Linear porokeratosis superimposed on disseminated superficial actinic porokeratosis: report of two cases exemplifying the concept of type 2 segmental manifestation of autosomal dominant skin disorders.

Freyschmidt-Paul P, Hoffmann R, König A, Happle R. Freyschmidt-Paul P, et al. Among authors: konig a. J Am Acad Dermatol. 1999 Oct;41(4):644-7. J Am Acad Dermatol. 1999. PMID: 10495390

9

Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome.

König A, Happle R, Bornholdt D, Engel H, Grzeschik KH. König A, et al. Am J Med Genet. 2000 Feb 14;90(4):339-46. Am J Med Genet. 2000. PMID: 10710235 Review.

10

An X-linked gene involved in androgenetic alopecia: a lesson to be learned from adrenoleukodystrophy.

König A, Happle R, Tchitcherina E, Schaefer JR, Sokolowski P, Köhler W, Hoffmann R. König A, et al. Dermatology. 2000;200(3):213-8. doi: 10.1159/000018385. Dermatology. 2000. PMID: 10828629

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,206 results

Search Page

Filters