Steijlen PM - Search Results

1

Genetic profiling of basal cell carcinomas detects postzygotic mosaicism in basal cell naevus syndrome.

Reinders MGHC, Cosgun B, Gijezen LMC, van Oosterhoud CN, Kelleners-Smeets NWJ, Vermander E, Vreeburg M, Steijlen PM, Mosterd K, van Geel M. Reinders MGHC, et al. Among authors: steijlen pm. Br J Dermatol. 2019 Sep;181(3):587-591. doi: 10.1111/bjd.17337. Epub 2018 Dec 5. Br J Dermatol. 2019. PMID: 30520020

2

Naevus corniculatus: a new acantholytic disorder.

Happle R, Steijlen PM, Kolde G. Happle R, et al. Among authors: steijlen pm. Br J Dermatol. 1990 Jan;122(1):107-12. doi: 10.1111/j.1365-2133.1990.tb08247.x. Br J Dermatol. 1990. PMID: 2297497

3

Acquired perforating dermatosis (Kyrle's disease).

De Mare S, Koopman RJ, Steijlen PM. De Mare S, et al. Among authors: steijlen pm. Br J Dermatol. 1993 Aug;129(2):211. Br J Dermatol. 1993. PMID: 7654587 No abstract available.

4

Becker's naevus with localized lipoatrophy and ipsilateral breast hypoplasia.

Van Gerwen HJ, Koopman RJ, Steijlen PM, Happle R. Van Gerwen HJ, et al. Among authors: steijlen pm. Br J Dermatol. 1993 Aug;129(2):213. Br J Dermatol. 1993. PMID: 7654589 No abstract available.

5

Sjögren-Larsson syndrome.

Der Kinderen DJ, Cruysberg JR, Steijlen PM. Der Kinderen DJ, et al. Among authors: steijlen pm. Br J Dermatol. 1993 Aug;129(2):213-4. Br J Dermatol. 1993. PMID: 7654590 No abstract available.

6

Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1.

Smith FJ, Del Monaco M, Steijlen PM, Munro CS, Morvay M, Coleman CM, Rietveld FJ, Uitto J, McLean WH. Smith FJ, et al. Among authors: steijlen pm. Br J Dermatol. 1999 Dec;141(6):1010-6. doi: 10.1046/j.1365-2133.1999.03198.x. Br J Dermatol. 1999. PMID: 10606845

7

Cutis marmorata telangiectatica congenita: report of 18 cases.

Gerritsen MJ, Steijlen PM, Brunner HG, Rieu P. Gerritsen MJ, et al. Among authors: steijlen pm. Br J Dermatol. 2000 Feb;142(2):366-9. doi: 10.1046/j.1365-2133.2000.03311.x. Br J Dermatol. 2000. PMID: 10730777 Review.

8

A case of Rombo syndrome.

van Steensel MA, Jaspers NG, Steijlen PM. van Steensel MA, et al. Among authors: steijlen pm. Br J Dermatol. 2001 Jun;144(6):1215-8. doi: 10.1046/j.1365-2133.2001.04235.x. Br J Dermatol. 2001. PMID: 11422044

9

Mal de Meleda without mutations in the ARS coding sequence.

van Steensel MA, van Geel MV, Steijlen PM. van Steensel MA, et al. Among authors: steijlen pm. Eur J Dermatol. 2002 Mar-Apr;12(2):129-32. Eur J Dermatol. 2002. PMID: 11872406

10

A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome.

van Steensel MA, van Geel M, Nahuys M, Smitt JH, Steijlen PM. van Steensel MA, et al. Among authors: steijlen pm. J Invest Dermatol. 2002 Apr;118(4):724-7. doi: 10.1046/j.1523-1747.2002.01735.x. J Invest Dermatol. 2002. PMID: 11918723 Free article.

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