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Browsing by Author Steijlen, P.M.

Full Text	Issue Date	Title	Author(s)
	2009	The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress.	Verstraeten, V.L.; Caputo, S.; Steensel, M.A.M. van; Duband-Goulet, I.; Zinn-Justin, S., et al
	2007	Novel EBP gene mutations in Conradi-Hunermann-Happle syndrome.	Steijlen, P.M.; Geel, M. van; Vreeburg, M.; Marcus-Soekarman, D.; Spaapen, L.J., et al
	2007	Oral R115866 in the treatment of moderate to severe plaque-type psoriasis.	Verfaille, C.J.; Thissen, C.A.; Bovenschen, H.J.; Mertens, J.; Steijlen, P.M., et al
	2006	The pathogenesis of hemangiomas: a review.	Bauland, C.G.; Steensel, M.A.M. van; Steijlen, P.M.; Rieu, P.N.M.A.; Spauwen, P.H.M.
	2006	Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation.	Verstraeten, V.L.; Broers, J.L.; Steensel, M.A.M. van; Zinn-Justin, S.; Ramaekers, F.C.S., et al
	2005	Further delineation of the hypotrichosis-deafness syndrome.	Steensel, M.A.M. van; Geel, M. van; Steijlen, P.M.
	2005	A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma.	Steensel, M.A.M. van; Spruijt, L.; Burgt, C.J.A. van der; Bladergroen, R.; Vermeer, M., et al
	2005	A missense mutation in the type II hair keratin hHb3 is associated with monilethrix.	Steensel, M.A.M. van; Steijlen, P.M.; Bladergroen, R.; Vermeer, M.; Geel, M. van
	2005	A new type of erythrokeratoderma.	Steensel, M.A.M. van; Geel, M. van; Steijlen, P.M.
	2004	Deficiency of tenascin-X causes abnormalities in dermal elastic fiber morphology.	Zweers, M.C.; Vlijmen-Willems, I.M.J.J. van; Kuppevelt, A.H.M.S.M. van; Mecham, R.P.; Steijlen, P.M., et al
	2004	New type of twin spot.	Steensel, M.A.M. van; Steijlen, P.M.; Maessen-Visch, M.B.
	2004	Cryptic splicing at a non-consensus splice-donor in a patient with a novel mutation in the plakophilin-1 gene.	Steijlen, P.M.; Steensel, M.A.M. van; Jansen, B.J.H.; Blokx, W.A.M.; Kerkhof, P.C.M. van de, et al
	2004	A phenotype resembling the Clouston syndrome with deafness is associated with a novel missense GJB2 mutation.	Steensel, M.A.M. van; Steijlen, P.M.; Bladergroen, R.; Hoefsloot, L.H.; Ravenswaaij-Arts, C.M.A. van, et al
	2004	Molecular genetics of hereditary hair and nail disease.	Steensel, M.A.M. van; Geel, M. van; Steijlen, P.M.
	2002	Genodermatologie : 'through the looking glass'	Steijlen, P.M.
	1998	Oral contraceptives in the treatment of Darier-White disease - a case report and review of the literature	Oostenbrink, J.H.; Cohen, E.B.; Steijlen, P.M.; Kerkhof, P.C.M. van de
	1997	Expression of filaggrin, involucrin and tenascin in monogenic disorders of keratinization	Gerritsen, M.J.P.; Kerkhof, P.C.M. van de; Vlijmen-Willems, I.M.J.J. van; Steijlen, P.M.
	1997	Patchy dermal hypoplasia as a characteristic feature of proteus syndrome	Happle, R.H.G.; Steijlen, P.M.; Theile, U.; Karitzky, D.; Tinschert, S., et al
	1997	Het congenitale angiodysplasiesyndroom van het type Klippel-Trenaunay; medische en psychologische aspecten	Boetes, C.; Boll, A.P.M.; Hartman, P.H.M.; Oostrom, C.G. van; Rieu, P.N.M.A., et al
	1997	De zweettest als diagnosticum op dragerschap van X-gebonden hypohidrotische ectodermale dysplasia (Christ-Siemens-Touraine-syndroom)	Lucker, G.P.H.; Steijlen, P.M.
	1997	Ehlers-Danlos-syndroom IV: variatie in fenotypen	Engels, C.H.A.M.; Dongen, P.W.J. van; Boers, G.H.J.; Steijlen, P.M.; Hamel, B.C.J.
	1997	The Huriez syndrome. Scleroatrophic palmoplantar keratoderma	Lucker, G.P.H.; Zeedijk, N.; Steijlen, P.M.
	1997	Molecular genetic approaches to skin disease : keratins and keratinisation	Steensel, M.A.M. van; Steijlen, P.M.; Rees, J.L.
	1997	Topical treatment of Darier's disease with 13-cis-retinoic acid. A clinical and immunohistochemical study.	Lucker, G.P.H.; Kerkhof, P.C.M. van de; Castelijns, F.A.; Steijlen, P.M.
	1997	Oral treatment of ichthyosis by the cytochrome P-450 inhibitor liarozole	Lucker, G.P.H.; Heremans, A.; Boegheim, P.J.; Kerkhof, P.C.M. van de; Steijlen, P.M.
	1997	Genetics of psoriasis	Steensel, M.A.M. van; Steijlen, P.M.
	1997	Sjogren-Larsson syndrome: clinical findings in eleven patients	Willemsen, M.A.A.P.; Domburg, P.H.M.F. van; Thijssen, H.O.M.; Cruysberg, J.R.M.; Steijlen, P.M., et al
	1997	Mapping of Papillon-Lefèvre syndrome to the chromosome 11q14 region	Fischer, J.; Blanchet-Bardon, C.; Prud'homme, J.-F.; Pavek, S.; Steijlen, P.M., et al
	1996	Ichthyosis	Steijlen, P.M.
	1996	Diphencyprone in the management of refractory palmoplantar and periungual warts : an open study	Rampen, F.H.J.; Steijlen, P.M.
	1996	Flow-cytometric investigation of epidermal cell characteristics in monogenic disorders of keratinization and their modulation by topical calcipotriol treatment	Lucker, G.P.H.; Steijlen, P.M.; Suykerbuyk, E.J.A.; Kragballe, K.; Brandrup, F., et al
	1996	Topical R-85355, a potent and selective 5-lipoxygenase inhibitor, fails to improve psoriasis	Kerkhof, P.C.M. van de; Pelt, J.P.A. van; Lucker, G.P.H.; Steijlen, P.M.; Heremans, A.
	1996	Acrodermatitis continua of Hallopeau in a patient with myelodysplastic syndrome	Kerkhof, P.C.M. van de; Steijlen, P.M.; Raymakers, R.A.P.
	1996	Possible indications for vitamin D3 analogues in conditions other than psoriasis vulgaris	Kerkhof, P.C.M. van de; Wittenhorst, M.; Gerritsen, M.J.P.; Jong, E.M.G.J. de; Lucker, G.P.H., et al
	1996	Toxic pustuloderma associated with clemastine therapy	Feind-Koopmans, A.G.; Valk, P.G.M. van der; Steijlen, P.M.; Kerkhof, P.C.M. van de
	1996	RET mutation screening in familial cutaneous lichen amyloidosis and in skin amyloidoses associated with multiple endocrine neoplasia	Hofstra, R.M.; Sijmons, R.H.; Stelwagen, T.; Stulp, R.P.; Kousseff, B.G, et al
	1996	A therapeutic approach to erythrodermic psoriasis: report of a case and a discussion of therapeutic options	Vleuten, C.J.M. van der; Gerritsen, M.J.P.; Steijlen, P.M.; Jong, E.M.G.J. de; Kerkhof, P.C.M. van de
	1996	Generalized atrophic benign epidermolysis bullosa : either 180-kd bullous pemphigoid antigen or laminin-5 deficiency	Jonkman, M.F.; Jong, M.C.J.M. de; Heeres, K.; Steijlen, P.M.; Owaribe, K., et al
	1996	Behandeling van dermatomycosen: lokaal of oraal	Steijlen, P.M.; Koopman, R.J.J.
	1996	Keratosis palmoplantaris varians et punctata	Lucker, G.P.H.; Steijlen, P.M.
	1996	Indikationen fur Vitamin-D3-Analoga bei nichtpsoriatischen Dermatosen	Kerkhof, P.C.M. van de; Wittenhorst, M.; Jong, E.M.G.J. de; Lucker, G.P.H.; Gerritsen, M.J.P., et al
	1996	Ichthyosis bullosa of Siemens : a distinct type of epidermolytic hyperkeratosis	Lenzner, U.; Happle, R.; Kremer, H.; Mensing, H.; Reinel, D., et al
	1995	Topical treatment of Sjögren-Larsson syndrome with calcipotriol	Lucker, G.P.H.; Kerkhof, P.C.M. van de; Cruysberg, J.R.M.; Kinderen, D.J. der; Steijlen, P.M.
	1995	Acrokeratosis paraneoplastica (Bazex syndrome) occuring with acquired ichthyosis in Hodgkin's disease	Lucker, G.P.H.; Steijlen, P.M.
	1995	Genodermatosen : keratinisatiestoornissen	Steijlen, P.M.
	1995	Topical treatment of ichthyoses with 13-cis retinoic acid : A clinical and immunohistochemical study	Lucker, G.P.H.; Kerkhof, P.C.M. van de; Castelijns, F.A.C.M.; Dijk, M.R. van; Schalkwijk, L.J.M., et al
	1995	Odonto-onycho-dermale dysplasie	Arnold, W.P.; Merkx, M.A.; Steijlen, P.M.
	1995	Efficacy, tolerability, and safety of calcipotriol ointment in disorders of keratinization	Kragballe, K.; Steijlen, P.M.; Henning Ibsen, H.; Kerkhof, P.C.M. van de; Esmann, J., et al
	1995	An unusual case of porokeratosis involving the natal cleft: porokeratosis ptychotropica?	Lucker, G.P.H.; Happle, R.H.G.; Steijlen, P.M.
	1995	Een aantal door geneesmiddelen veroorzaakte dermatosen : erythema exsudativum multiforme	Steijlen, P.M.