Steijlen PM - Search Results

1

Clouston syndrome can mimic pachyonychia congenita.

van Steensel MA, Jonkman MF, van Geel M, Steijlen PM, McLean WH, Smith FJ. van Steensel MA, et al. Among authors: steijlen pm. J Invest Dermatol. 2003 Nov;121(5):1035-8. doi: 10.1046/j.1523-1747.2003.12527.x. J Invest Dermatol. 2003. PMID: 14708603 Free article.

2

Genetic linkage between the collagen VII (COL7A1) gene and the autosomal dominant form of dystrophic epidermolysis bullosa in two Dutch kindreds.

Gruis NA, Bavinck JN, Steijlen PM, van der Schroeff JG, van Haeringen A, Happle R, Mariman E, van Beersum SE, Uitto J, Vermeer BJ, et al. Gruis NA, et al. Among authors: steijlen pm. J Invest Dermatol. 1992 Nov;99(5):528-30. doi: 10.1111/1523-1747.ep12658066. J Invest Dermatol. 1992. PMID: 1358979 Free article.

3

Enzymatic distinction between two subgroups of autosomal recessive lamellar ichthyosis.

Bergers M, Traupe H, Dünnwald SC, Mier PD, van Dooren-Greebe R, Steijlen P, Happle R. Bergers M, et al. J Invest Dermatol. 1990 Apr;94(4):407-12. doi: 10.1111/1523-1747.ep12874475. J Invest Dermatol. 1990. PMID: 2107261 Free article.

4

Genetic linkage of the keratin type II gene cluster with ichthyosis bullosa of Siemens and with autosomal dominant ichthyosis exfoliativa.

Steijlen PM, Kremer H, Vakilzadeh F, Happle R, Lavrijsen AP, Ropers HH, Mariman EC. Steijlen PM, et al. J Invest Dermatol. 1994 Sep;103(3):282-5. doi: 10.1111/1523-1747.ep12394335. J Invest Dermatol. 1994. PMID: 7521372 Free article.

5

Aplasia cutis congenita and associated disorders: an update.

Evers ME, Steijlen PM, Hamel BC. Evers ME, et al. Among authors: steijlen pm. Clin Genet. 1995 Jun;47(6):295-301. doi: 10.1111/j.1399-0004.1995.tb03968.x. Clin Genet. 1995. PMID: 7554362

6

Pachyonychia congenita tarda.

Lucker GP, Steijlen PM. Lucker GP, et al. Among authors: steijlen pm. Clin Exp Dermatol. 1995 May;20(3):226-9. doi: 10.1111/j.1365-2230.1995.tb01307.x. Clin Exp Dermatol. 1995. PMID: 7671418 Free article.

7

Mosaic expression of hypohidrotic ectodermal dysplasia in an isolated affected female child.

Bartstra HL, Hulsmans RF, Steijlen PM, Ruige M, de Die-Smulders CE, Cassiman JJ. Bartstra HL, et al. Among authors: steijlen pm. Arch Dermatol. 1994 Nov;130(11):1421-4. Arch Dermatol. 1994. PMID: 7979445

8

Ichthyosis bullosa of Siemens is caused by mutations in the keratin 2e gene.

Kremer H, Zeeuwen P, McLean WH, Mariman EC, Lane EB, van de Kerkhof CM, Ropers HH, Steijlen PM. Kremer H, et al. Among authors: steijlen pm. J Invest Dermatol. 1994 Sep;103(3):286-9. doi: 10.1111/1523-1747.ep12394414. J Invest Dermatol. 1994. PMID: 8077693 Free article.

9

Congenital atrichia, palmoplantar hyperkeratosis, mental retardation, and early loss of teeth in four siblings: a new syndrome?

Steijlen PM, Neumann HA, der Kinderen DJ, Smeets DF, van der Kerkhof PC, Happle R. Steijlen PM, et al. J Am Acad Dermatol. 1994 May;30(5 Pt 2):893-8. doi: 10.1016/s0190-9622(94)70108-3. J Am Acad Dermatol. 1994. PMID: 8169270 Review.

10

Pachyonychia congenita in the absence of other syndrome abnormalities.

Chang A, Lucker GP, van de Kerkhof PC, Steijlen PM. Chang A, et al. Among authors: steijlen pm. J Am Acad Dermatol. 1994 Jun;30(6):1017-8. doi: 10.1016/s0190-9622(09)80144-8. J Am Acad Dermatol. 1994. PMID: 8188864 No abstract available.

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