Steijlen PM - Search Results

1

A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.

Schalkwijk J, Zweers MC, Steijlen PM, Dean WB, Taylor G, van Vlijmen IM, van Haren B, Miller WL, Bristow J. Schalkwijk J, et al. Among authors: steijlen pm. N Engl J Med. 2001 Oct 18;345(16):1167-75. doi: 10.1056/NEJMoa002939. N Engl J Med. 2001. PMID: 11642233 Free article.

2

Deficiency of tenascin-X causes abnormalities in dermal elastic fiber morphology.

Zweers MC, van Vlijmen-Willems IM, van Kuppevelt TH, Mecham RP, Steijlen PM, Bristow J, Schalkwijk J. Zweers MC, et al. Among authors: steijlen pm. J Invest Dermatol. 2004 Apr;122(4):885-91. doi: 10.1111/j.0022-202X.2004.22401.x. J Invest Dermatol. 2004. PMID: 15102077 Free article.

3

Expression of tenascin, biglycan and decorin in disorders of keratinization.

Steijlen PM, Maessen E, Kresse H, Van Vlijmen IM, Verstraeten AA, Traupe H, Schalkwijk J. Steijlen PM, et al. Br J Dermatol. 1994 May;130(5):564-8. doi: 10.1111/j.1365-2133.1994.tb13100.x. Br J Dermatol. 1994. PMID: 7515636

4

Haploinsufficiency of TNXB is associated with hypermobility type of Ehlers-Danlos syndrome.

Zweers MC, Bristow J, Steijlen PM, Dean WB, Hamel BC, Otero M, Kucharekova M, Boezeman JB, Schalkwijk J. Zweers MC, et al. Among authors: steijlen pm. Am J Hum Genet. 2003 Jul;73(1):214-7. doi: 10.1086/376564. Am J Hum Genet. 2003. PMID: 12865992 Free PMC article. No abstract available.

5

Tenascin expression in human dermis is related to epidermal proliferation.

Schalkwijk J, Steijlen PM, van Vlijmen-Willems IM, Oosterling B, Mackie EJ, Verstraeten AA. Schalkwijk J, et al. Among authors: steijlen pm. Am J Pathol. 1991 Nov;139(5):1143-50. Am J Pathol. 1991. PMID: 1719820 Free PMC article.

6

Ehlers-Danlos syndrome and type III collagen abnormalities: a variable clinical spectrum.

Hamel BC, Pals G, Engels CH, van den Akker E, Boers GH, van Dongen PW, Steijlen PM. Hamel BC, et al. Among authors: steijlen pm. Clin Genet. 1998 Jun;53(6):440-6. doi: 10.1111/j.1399-0004.1998.tb02592.x. Clin Genet. 1998. PMID: 9712532

7

[Ehlers-Danlos syndrome IV: phenotype variation].

Engels CH, van Dongen PW, Boers GH, Steijlen PM, Hamel BC. Engels CH, et al. Among authors: steijlen pm. Ned Tijdschr Geneeskd. 1997 Feb 8;141(6):296-8. Ned Tijdschr Geneeskd. 1997. PMID: 9148166 Dutch.

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

IgA deficiency and psoriasis: relevance of IgA in the pathogenesis of psoriasis.

van de Kerkhof PC, Steijlen PM. van de Kerkhof PC, et al. Among authors: steijlen pm. Dermatology. 1995;191(1):46-8. doi: 10.1159/000246487. Dermatology. 1995. PMID: 8589483

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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