Steijlen PM - Search Results

1

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

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

Restrictive dermopathy in two brothers.

Happle R, Stekhoven JH, Hamel BC, Kollée LA, Nijhuis JG, Anton-Lamprecht I, Steijlen PM. Happle R, et al. Among authors: steijlen pm. Arch Dermatol. 1992 Feb;128(2):232-5. Arch Dermatol. 1992. PMID: 1739303

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

Efficacy, tolerability, and safety of calcipotriol ointment in disorders of keratinization. Results of a randomized, double-blind, vehicle-controlled, right/left comparative study.

Kragballe K, Steijlen PM, Ibsen HH, van de Kerkhof PC, Esmann J, Sorensen LH, Axelsen MB. Kragballe K, et al. Among authors: steijlen pm. Arch Dermatol. 1995 May;131(5):556-60. Arch Dermatol. 1995. PMID: 7741542 Clinical Trial.

6

The hereditary palmoplantar keratoses: an updated review and classification.

Lucker GP, Van de Kerkhof PC, Steijlen PM. Lucker GP, et al. Among authors: steijlen pm. Br J Dermatol. 1994 Jul;131(1):1-14. doi: 10.1111/j.1365-2133.1994.tb08450.x. Br J Dermatol. 1994. PMID: 8043399 Review.

7

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.

8

Variant of odontoonychodermal dysplasia?

Arnold WP, Merkx MA, Steijlen PM. Arnold WP, et al. Among authors: steijlen pm. Am J Med Genet. 1995 Nov 6;59(2):242-4. doi: 10.1002/ajmg.1320590224. Am J Med Genet. 1995. PMID: 8588594 No abstract available.

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: steijlen pm. Arch Dermatol. 1996 Feb;132(2):145-50. doi: 10.1001/archderm.132.2.145. Arch Dermatol. 1996. PMID: 8629821 Free article.

10

Restrictive dermopathy. Report of 12 cases. Dutch Task Force on Genodermatology.

Smitt JH, van Asperen CJ, Niessen CM, Beemer FA, van Essen AJ, Hulsmans RF, Oranje AP, Steijlen PM, Wesby-van Swaay E, Tamminga P, Breslau-Siderius EJ. Smitt JH, et al. Among authors: steijlen pm. Arch Dermatol. 1998 May;134(5):577-9. doi: 10.1001/archderm.134.5.577. Arch Dermatol. 1998. PMID: 9606327 Review.

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