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P M Steijlen

Showing results (111-120 of 145) with videos related to

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The Journal of Investigative Dermatology|September 1, 1994
Ichthyosis bullosa of Siemens is caused by mutations in the keratin 2e geneH Kremer, P Zeeuwen, W H McLean, et al.
Journal of Vascular Surgery|October 23, 2001
Evolution of deep venous thrombosis: a 2-year follow-up using duplex ultrasound scan and strain-gauge plethysmographyJ H Haenen, H Wollersheim, M C Janssen, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 29, 1997
[Klippel-Trenaunay-type congenital angiodysplasia syndrome; medical and psychological aspects]C Boetes, A P Boll, P H Hartman, et al.
The British Journal of Dermatology|January 12, 2011
Linkage refinement of Bazex-Dupré-Christol syndrome to an 11·4-Mb interval on chromosome Xq25-27.1L J M T Parren, F Abuzahra, T Wagenvoort, et al.
The British Journal of Dermatology|February 19, 2010
Phenotypic variability associated with WNT10A nonsense mutationsM Van Geel, M Gattas, Y Kesler, et al.
The New England Journal of Medicine|October 20, 2001
A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiencyJ Schalkwijk, M C Zweers, P M Steijlen, et al.
The British Journal of Dermatology|December 22, 1999
Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1F J Smith, M Del Monaco, P M Steijlen, et al.
The British Journal of Dermatology|October 12, 2011
Clinically manifest X-linked recessive ichthyosis in a female due to a homozygous interstitial 1·6-Mb deletion of Xp22.31I F Nagtzaam, A P A Stegmann, P M Steijlen, et al.
Archives of Dermatological Research|January 1, 1993
Topical treatment of ichthyoses and Darier's disease with 13-cis-retinoic acid. A clinical and immunohistochemical studyP M Steijlen, D O Reifenschweiler, F C Ramaekers, et al.
The British Journal of Dermatology|September 22, 2010
A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndromeE A de Zwart-Storm, M van Geel, E Veysey, et al.
Pageof 15

Showing results (111-120 of 145) with videos related to

Sort By:
Pageof 15
The Journal of Investigative Dermatology|September 1, 1994
Ichthyosis bullosa of Siemens is caused by mutations in the keratin 2e geneH Kremer, P Zeeuwen, W H McLean, et al.
Journal of Vascular Surgery|October 23, 2001
Evolution of deep venous thrombosis: a 2-year follow-up using duplex ultrasound scan and strain-gauge plethysmographyJ H Haenen, H Wollersheim, M C Janssen, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 29, 1997
[Klippel-Trenaunay-type congenital angiodysplasia syndrome; medical and psychological aspects]C Boetes, A P Boll, P H Hartman, et al.
The British Journal of Dermatology|January 12, 2011
Linkage refinement of Bazex-Dupré-Christol syndrome to an 11·4-Mb interval on chromosome Xq25-27.1L J M T Parren, F Abuzahra, T Wagenvoort, et al.
The British Journal of Dermatology|February 19, 2010
Phenotypic variability associated with WNT10A nonsense mutationsM Van Geel, M Gattas, Y Kesler, et al.
The New England Journal of Medicine|October 20, 2001
A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiencyJ Schalkwijk, M C Zweers, P M Steijlen, et al.
The British Journal of Dermatology|December 22, 1999
Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1F J Smith, M Del Monaco, P M Steijlen, et al.
The British Journal of Dermatology|October 12, 2011
Clinically manifest X-linked recessive ichthyosis in a female due to a homozygous interstitial 1·6-Mb deletion of Xp22.31I F Nagtzaam, A P A Stegmann, P M Steijlen, et al.
Archives of Dermatological Research|January 1, 1993
Topical treatment of ichthyoses and Darier's disease with 13-cis-retinoic acid. A clinical and immunohistochemical studyP M Steijlen, D O Reifenschweiler, F C Ramaekers, et al.
The British Journal of Dermatology|September 22, 2010
A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndromeE A de Zwart-Storm, M van Geel, E Veysey, et al.
Pageof 15