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Peter Steijlen

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Jennifer A Easton; Rudolf Happle; René Janssens; Miriam A F Kamps; Patricia E Martin; Peter M Steijlen; Gianluca Tadini; Michel van Geel; Steven Donnelly; Maurice A M van Steensel
Porokeratotic eccrine nevus may be caused by somatic connexin26 mutations.
A M van Tuyll van Serooskerken; Louise Warnich; Reno S Bladergroen; B I Drögemöller; Pamela Poblete Gutiérrez; Peter M Steijlen; K Te Velde; Michel van Geel; C J van Heerden; Jorge Frank
Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestry.
Anne Moniek van Tuyll van Serooskerken; J H Paul Wilson; Jens M Baron; Reno S Bladergroen; Felix W de Rooij; Annie Edixhoven; Sylvia Joussen; Rita H Koole; Hans F Merk; Pamela Poblete Gutiérrez; Peter M Steijlen; Kornelis te Velde; Michel van Geel; Jorge Frank
Digenic inheritance of mutations in the coproporphyrinogen oxidase and protoporphyrinogen oxidase genes in a unique type of porphyria.

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All Publications

2012: Jennifer A Easton; Rudolf Happle; René Janssens; Miriam A F Kamps; Patricia E Martin; Peter M Steijlen; Gianluca Tadini; Michel van Geel; Steven Donnelly; Maurice A M van Steensel
Porokeratotic eccrine nevus may be caused by somatic connexin26 mutations.
The Journal of investigative dermatology 2012;132(9):2184-91.
2012: A M van Tuyll van Serooskerken; Louise Warnich; Reno S Bladergroen; B I Drögemöller; Pamela Poblete Gutiérrez; Peter M Steijlen; K Te Velde; Michel van Geel; C J van Heerden; Jorge Frank
Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestry.
The British journal of dermatology 2012;166(2):261-5.
2011: Anne Moniek van Tuyll van Serooskerken; J H Paul Wilson; Jens M Baron; Reno S Bladergroen; Felix W de Rooij; Annie Edixhoven; Sylvia Joussen; Rita H Koole; Hans F Merk; Pamela Poblete Gutiérrez; Peter M Steijlen; Kornelis te Velde; Michel van Geel; Jorge Frank
Digenic inheritance of mutations in the coproporphyrinogen oxidase and protoporphyrinogen oxidase genes in a unique type of porphyria.
The Journal of investigative dermatology 2011;131(11):2249-54.
2011: Martin Glatz; Peter M Steijlen; Michel van Geel; Maurice A M van Steensel; Peter Wolf
An unusual missense mutation in the GJB3 gene resulting in severe erythrokeratodermia variabilis.
Acta dermato-venereologica 2011;91(6):714-5.
2011: L J M T Parren; Peter M Steijlen; Michel van Geel; Maurice A M van Steensel; T Wagenvoort; Faris Abuzahra; F Koene; Jorge Frank
Linkage refinement of Bazex-Dupré-Christol syndrome to an 11·4-Mb interval on chromosome Xq25-27.1.
The British journal of dermatology 2011;165(1):201-3.
2011: Valerie L R M Verstraeten; Johan Renes; Frans C S Ramaekers; Miriam Kamps; Helma J Kuijpers; Fons Verheyen; Martin Wabitsch; Peter M Steijlen; Maurice A M van Steensel; Jos L V Broers
Reorganization of the nuclear lamina and cytoskeleton in adipogenesis.
Histochemistry and cell biology 2011;135(3):251-61.
2011: Klara Mosterd; Monique R T M Thissen; Arienne M W van Marion; Patty J Nelemans; Bjorn G P M Lohman; Peter M Steijlen; Nicole W J Kelleners-Smeets
Correlation between histologic findings on punch biopsy specimens and subsequent excision specimens in recurrent basal cell carcinoma.
Journal of the American Academy of Dermatology 2011;64(2):323-7.
2011: E A de Zwart-Storm; M van Geel; E Veysey; Susan Burge; S Cooper; Peter M Steijlen; P E Martin; Maurice A M van Steensel
A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome.
The British journal of dermatology 2011;164(1):197-9.
2010: I F Nagtzaam; Michel van Geel; A Driessen; Peter M Steijlen; Maurice A M van Steensel
Bile duct paucity is part of the neonatal ichthyosis-sclerosing cholangitis phenotype.
The British journal of dermatology 2010;163(1):205-7.
2010: Michel van Geel; M Gattas; Y Kesler; P Tong; H Yan; K Tran; Peter M Steijlen; Dédée F Murrell; Maurice A M van Steensel
Phenotypic variability associated with WNT10A nonsense mutations.
The British journal of dermatology 2010;162(6):1403-6.
2009: Maurice A M van Steensel; R J Damstra; Martijn Heitink; R S Bladergroen; J Veraart; Peter M Steijlen; M van Geel
Novel missense mutations in the FOXC2 gene alter transcriptional activity.
Human mutation 2009;30(12):E1002-9.
2009: Valerie L R M Verstraeten; Sandrine Caputo; Maurice A M van Steensel; Isabelle Duband-Goulet; Sophie Zinn-Justin; Miriam Kamps; Helma J H Kuijpers; Cecilia Ostlund; Howard J Worman; Jacob J Briedé; Caroline Le Dour; Carlo L M Marcelis; Michel van Geel; Peter M Steijlen; Arthur van den Wijngaard; Frans C S Ramaekers; Jos L V Broers
The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress.
Journal of cellular and molecular medicine 2009;13(5):959-71.
2009: R G L Nellen; Michel van Geel; Peter M Steijlen; Maurice A M van Steensel
Compound heterozygosity for ARS component B mutations in a Dutch patient with mal de Meleda.
The British journal of dermatology 2009;160(4):878-80.
2009: Sadhanna Badeloe; K Y van Spaendonck-Zwarts; Maurice A M van Steensel; A M W van Marion; A J van Essen; Marcel F Jonkman; Peter M Steijlen; Pamela Poblete Gutiérrez; Michel van Geel; Jorge Frank
Wilms tumour as a possible early manifestation of hereditary leiomyomatosis and renal cell cancer?
The British journal of dermatology 2009;160(3):707-9.
2009: Valerie L R M Verstraeten; Wolfgang Holnthoner; Maurice A M van Steensel; Joep C J M Veraart; Reno S Bladergroen; Caroline A Heckman; Salla Keskitalo; Jorge Frank; Kari Alitalo; Michel van Geel; Peter M Steijlen
Functional analysis of FLT4 mutations associated with Nonne-Milroy lymphedema.
The Journal of investigative dermatology 2009;129(2):509-12.
2008: Klara Mosterd; G A M Krekels; Fred Hm Nieman; Judith U Ostertag; Brigitte A B Essers; Carmen D Dirksen; Peter M Steijlen; Anton Vermeulen; Ham Neumann; Nicole W J Kelleners-Smeets
Surgical excision versus Mohs' micrographic surgery for primary and recurrent basal-cell carcinoma of the face: a prospective randomised controlled trial with 5-years' follow-up.
The lancet oncology 2008;9(12):1149-56.
2008: Maurice A M van Steensel; Sadhanna Badeloe; V Winnepenninckx; M Vreeburg; Peter M Steijlen; Michel van Geel
Granulomatous rosacea and Crohn's disease in a patient homozygous for the Crohn-associated NOD2/CARD15 polymorphism R702W.
Experimental dermatology 2008;17(12):1057-8.
2008: Ruud G L Nellen; Ariënne M W van Marion; Jorge Frank; Pamela Poblete Gutiérrez; Peter M Steijlen
Eruption of lymphocyte recovery or autologous graft-versus-host disease?
International journal of dermatology 2008;47 Suppl 1():32-4.
2008: Eugene A de Zwart-Storm; Michel van Geel; Pierre A F A van Neer; Peter M Steijlen; Patricia E Martin; Maurice A M van Steensel
A novel missense mutation in the second extracellular domain of GJB2, p.Ser183Phe, causes a syndrome of focal palmoplantar keratoderma with deafness.
The American journal of pathology 2008;173(4):1113-9.
2008: K Mosterd; M R T M Thissen; Patricia J Nelemans; N W J Kelleners-Smeets; R L L T Janssen; K G M E Broekhof; H A M Neumann; Peter M Steijlen; D I M Kuijpers
Fractionated 5-aminolaevulinic acid-photodynamic therapy vs. surgical excision in the treatment of nodular basal cell carcinoma: results of a randomized controlled trial.
The British journal of dermatology 2008;159(4):864-70.
2008: Maurice A M van Steensel; V Winnepenninckx; Ivo F Nagtzaam; R Janssens; R De Vos; Peter M Steijlen
A case of Lelis syndrome with hystrix-like ichthyosis.
American journal of medical genetics. Part A 2008;146A(16):2155-8.
2008: Sadhanna Badeloe; Reno S Bladergroen; Marcel F Jonkman; Nigel P Burrows; Peter M Steijlen; Pamela Poblete Gutiérrez; Maurice A M van Steensel; Michel van Geel; Jorge Frank
Hereditary multiple cutaneous leiomyoma resulting from novel mutations in the fumarate hydratase gene.
Journal of dermatological science 2008;51(2):139-43.
2008: Roeland P M Ceulen; Ariënne M W van Marion; Peter M Steijlen; Jorge Frank; Pamela Poblete Gutiérrez
Multiple unilateral skin tumors suggest type 1 segmental manifestation of familial syringoma.
European journal of dermatology : EJD 2008;18(3):285-8.
2008: Janna Nousbeck; Ronen Spiegel; Akemi Ishida-Yamamoto; Margarita Indelman; Ayelet Shani-Adir; Noam Adir; Ehud Lipkin; Sivan Bercovici; Dan Geiger; Maurice A M van Steensel; Peter M Steijlen; Reuven Bergman; Albrecht Bindereif; Mordechai Choder; Stavit Shalev; Eli Sprecher
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesis.
American journal of human genetics 2008;82(5):1114-21.
2008: Laurent Parmentier; Peter M Steijlen; Maurice A M van Steensel
Recessive palmoplantar keratodermas: a fertile biological hunting ground.
Archives of dermatology 2008;144(3):384-5.
2007: Peter M Steijlen; Michel van Geel; M Vreeburg; Dominique Marcus-Soekarman; L J M Spaapen; F C M Castelijns; M Willemsen; Maurice A M van Steensel
Novel EBP gene mutations in Conradi-Hünermann-Happle syndrome.
The British journal of dermatology 2007;157(6):1225-9.
2007: Maurice A M van Steensel; Michel van Geel; C T R M Schrander-Stumpel; Peter M Steijlen; J C J M Veraart
Lymphedema, cardiac septal defects, and characteristic facies: possible new case of Irons-Bianchi syndrome.
American journal of medical genetics. Part A 2007;143A(20):2448-51.
2007: Aileen Sandilands; Ana Terron-Kwiatkowski; Peter R Hull; Gráinne M O'Regan; Timothy H Clayton; Rosemarie M Watson; Thomas Carrick; Alan T Evans; Haihui Liao; Yiwei Zhao; Linda E Campbell; Matthias Schmuth; Robert Gruber; Andreas R Janecke; Peter M Elias; Maurice A M van Steensel; Ivo Nagtzaam; Michel van Geel; Peter M Steijlen; Colin S Munro; Daniel G Bradley; Colin N A Palmer; Frances J D Smith; W H Irwin McLean; Alan D Irvine
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.
Nature genetics 2007;39(5):650-4.
2007: Maurice A M van Steensel; Valerie L R M Verstraeten; Jorge Frank; Nicole W J Kelleners-Smeets; Pamela Poblete Gutiérrez; Dominique Marcus-Soekarman; Reno S Bladergroen; Peter M Steijlen; Michel van Geel
Novel mutations in the BHD gene and absence of loss of heterozygosity in fibrofolliculomas of Birt-Hogg-Dubé patients.
The Journal of investigative dermatology 2007;127(3):588-93.
2007: Sadhanna Badeloe; Michel van Geel; Maurice A M van Steensel; Peter M Steijlen; Pamela Poblete Gutiérrez; J A Frank
[From gene to disease; cutaneous leiomyomatosis].
Nederlands tijdschrift voor geneeskunde 2007;151(5):300-4.
2006: Vinzenz Oji; Juliette Mazereeuw Hautier; Bijan Ahvazi; Ingrid Hausser; Karin Aufenvenne; Tatjana Walker; Natalia Seller; Peter M Steijlen; Wolfgang Küster; Alain Hovnanian; Hans Christian Hennies; Heiko Traupe
Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype.
Human molecular genetics 2006;15(21):3083-97.
2006: Sadhanna Badeloe; Michel van Geel; Maurice A M van Steensel; Jesús Bastida; Juan Ferrando; Peter M Steijlen; Jorge Frank; Pamela Poblete Gutiérrez
Diffuse and segmental variants of cutaneous leiomyomatosis: novel mutations in the fumarate hydratase gene and review of the literature.
Experimental dermatology 2006;15(9):735-41.
2006: Valerie L R M Verstraeten; Jos L V Broers; Maurice A M van Steensel; Sophie Zinn-Justin; Frans C S Ramaekers; Peter M Steijlen; Miriam Kamps; Helma J H Kuijpers; Diane Merckx; H J M Smeets; Raoul Hennekam; Carlo L M Marcelis; Arthur van den Wijngaard
Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation.
Human molecular genetics 2006;15(16):2509-22.
2006: Ana Terron-Kwiatkowski; Maurice A M van Steensel; Michel van Geel; E Birgitte Lane; W H Irwin McLean; Peter M Steijlen
Mutation S233L in the 1B domain of keratin 1 causes epidermolytic palmoplantar keratoderma with "tonotubular" keratin.
The Journal of investigative dermatology 2006;126(3):607-13.
2006: Constantijn G Bauland; Maurice A M van Steensel; Peter M Steijlen; Paul N M A Rieu; Paul H M Spauwen
The pathogenesis of hemangiomas: a review.
Plastic and reconstructive surgery 2006;117(2):29e-35e.
2005: Andrew J Cassidy; Maurice A M van Steensel; Peter M Steijlen; Michel van Geel; Jaap van der Velden; Susan M Morley; Alessandro Terrinoni; Gerry Melino; Eleonora Candi; W H Irwin McLean
A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome.
American journal of human genetics 2005;77(6):909-17.
2005: Maurice A M van Steensel; M Vreeburg; Peter M Steijlen; C E M de Die-Smulders
Myhre syndrome in a female with previously undescribed symptoms: further delineation of the phenotype.
American journal of medical genetics. Part A 2005;139A(2):127-30.
2005: Maurice A M van Steensel; Michel van Geel; Peter M Steijlen
Further delineation of the hypotrichosis-deafness syndrome.
European journal of dermatology : EJD 2005;15(6):437-8.
2005: Maurice A M van Steensel; Peter M Steijlen; Reno S Bladergroen; M Vermeer; Michel van Geel
A missense mutation in the type II hair keratin hHb3 is associated with monilethrix.
Journal of medical genetics 2005;42(3):e19.
2005: Maurice A M van Steensel; Liesbeth Spruijt; I van der Burgt; Reno S Bladergroen; M Vermeer; Peter M Steijlen; Michel van Geel
A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma.
American journal of medical genetics. Part A 2005;132A(2):171-4.
2005: Maurice A M van Steensel; Michel van Geel; Peter M Steijlen
A new type of erythrokeratoderma.
The British journal of dermatology 2005;152(1):155-8.
2004: Maurice A M van Steensel; Michel van Geel; Peter M Steijlen
Molecular genetics of hereditary hair and nail disease.
American journal of medical genetics. Part C, Seminars in medical genetics 2004;131C(1):52-60.
2004: Maurice A M van Steensel; Peter M Steijlen; Reno S Bladergroen; Lies Hoefsloot; Conny van Ravenswaaij-Arts; Michel van Geel
A phenotype resembling the Clouston syndrome with deafness is associated with a novel missense GJB2 mutation.
The Journal of investigative dermatology 2004;123(2):291-3.
2004: Peter M Steijlen; Maurice A M van Steensel; Bastiaan Jan Herman Jansen; Willeke A M Blokx; P C M van de Kerkhof; Rudolf Happle; Michel van Geel
Cryptic splicing at a non-consensus splice-donor in a patient with a novel mutation in the plakophilin-1 gene.
The Journal of investigative dermatology 2004;122(5):1321-4.
2004: Manon C Zweers; Ivonne M J J van Vlijmen-Willems; Toin H van Kuppevelt; Robert P Mecham; Peter M Steijlen; James Bristow; Joost Schalkwijk
Deficiency of tenascin-X causes abnormalities in dermal elastic fiber morphology.
The Journal of investigative dermatology 2004;122(4):885-91.
2003: Maurice A M van Steensel; Marcel F Jonkman; Michel van Geel; Peter M Steijlen; W H Irwin McLean; Frances J D Smith
Clouston syndrome can mimic pachyonychia congenita.
The Journal of investigative dermatology 2003;121(5):1035-8.
2003: Manon C Zweers; James Bristow; Peter M Steijlen; Willow B Dean; Ben C Hamel; Marisol Otero; Martina Kucharekova; Jan B M Boezeman; Joost Schalkwijk
Haploinsufficiency of TNXB is associated with hypermobility type of Ehlers-Danlos syndrome.
American journal of human genetics 2003;73(1):214-7.
2003: Alexandre Irrthum; koenraad devriendt; David Chitayat; Gert Matthijs; Conrad Glade; Peter M Steijlen; Jean-Pierre Fryns; Maurice A M van Steensel; Miikka Vikkula
Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.
American journal of human genetics 2003;72(6):1470-8.
2003: W H P M Vissers; Maurice A M van Steensel; Peter M Steijlen; Willy O Renier; P C M van de Kerkhof; Carine Van Der Vleuten
Klippel-Trenaunay syndrome and Sturge-Weber syndrome: variations on a theme?
European journal of dermatology : EJD 2003;13(3):238-41.
2002: Michel van Geel; Maurice A M van Steensel; Peter M Steijlen
Connexin 30.3 (GJB4) is not required for normal skin function in humans.
The British journal of dermatology 2002;147(6):1275-7.
2002: Maurice A M van Steensel; Michel van Geel; Peter M Steijlen
New syndrome of hypotrichosis, striate palmoplantar keratoderma, acro-osteolysis and periodontitis not due to mutations in cathepsin C.
The British journal of dermatology 2002;147(3):575-81.
2002: Johan Toonstra; Jan G Lier; Peter M Steijlen; P C M van de Kerkhof
Graft-versus-host disease-like eruption preceding a nodal CD30+ lymphoma.
European journal of dermatology : EJD 2002;12(4):364-6.
2002: H P Zweep; Paul N M A Rieu; CE van Die; A P M Boll; Peter M Steijlen; Paul H M Spauwen
[Haemangiomas and congenital vascular malformations: their classification and diagnosis].
Nederlands tijdschrift voor geneeskunde 2002;146(23):1072-7.
2002: Michel van Geel; Maurice A M van Steensel; Wolfgang Küster; Hans Christian Hennies; Rudolf Happle; Peter M Steijlen; A König
HID and KID syndromes are associated with the same connexin 26 mutation.
The British journal of dermatology 2002;146(6):938-42.
2002: Takahiro Hamada; W H Irwin McLean; Michele Ramsay; G H S Ashton; Arti Nanda; Trefor Jenkins; Isobel Edelstein; Andrew P South; Oliver Bleck; Vesarat Wessagowit; Rajeev Mallipeddi; Guy E Orchard; Hong Wan; Patricia Dopping-Hepenstal; Jemima E Mellerio; Neil Whittock; Colin S Munro; Maurice A M van Steensel; Peter M Steijlen; Jian Ni; Lurong Zhang; Takashi Hashimoto; Robin A J Eady; John A McGrath
Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1).
Human molecular genetics 2002;11(7):833-40.
2002: Maurice A M van Steensel; Michel van Geel; Marc Nahuys; J H Sillevis Smitt; Peter M Steijlen
A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome.
The Journal of investigative dermatology 2002;118(4):724-7.
2002: Maurice A M van Steensel; Michel van Geel; Peter M Steijlen
Mal de Meleda without mutations in the ARS coding sequence.
European journal of dermatology : EJD 2002;12(2):129-32.
2001: C Glade; Maurice A M van Steensel; Peter M Steijlen
Hypotrichosis, lymphedema of the legs and acral telangiectasias--new syndrome?
European journal of dermatology : EJD 2001;11(6):515-7.
2001: Joost Schalkwijk; Manon C Zweers; Peter M Steijlen; Willow B Dean; Glen Taylor; I M van Vlijmen; B van Haren; W L Miller; James Bristow
A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.
The New England journal of medicine 2001;345(16):1167-75.
2001: Maurice A M van Steensel; M I Koedam; O Q J Swinkels; F Rietveld; Peter M Steijlen
Woolly hair, premature loss of teeth, nail dystrophy, acral hyperkeratosis and facial abnormalities: possible new syndrome in a Dutch kindred.
The British journal of dermatology 2001;145(1):157-61.
2001: Maurice A M van Steensel; N G Jaspers; Peter M Steijlen
A case of Rombo syndrome.
The British journal of dermatology 2001;144(6):1215-8.
2001: Maurice A M van Steensel; Frances J D Smith; Peter M Steijlen
A new type of pachyonychia congenita.
European journal of dermatology : EJD 2001;11(3):188-90.
2000: Peter M Steijlen; HE Viëtor; Maurice A M van Steensel; Rudolf Happle
Sweat testing in hypomelanosis of Ito: divergent results reflecting genetic heterogeneity.
European journal of dermatology : EJD 2000;10(3):217-9.
2000: M J P Gerritsen; Peter M Steijlen; H G Brunner; P Rieu
Cutis marmorata telangiectatica congenita: report of 18 cases.
The British journal of dermatology 2000;142(2):366-9.
2000: Maurice A M van Steensel; Rudolf Happle; Peter M Steijlen
Molecular genetics of the hair follicle: the state of the art.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.) 2000;223(1):1-7.
1999: Frances J D Smith; M Del Monaco; Peter M Steijlen; Colin S Munro; M Morvay; CM Coleman; F J Rietveld; Jouni Uitto; W H Irwin McLean
Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1.
The British journal of dermatology 1999;141(6):1010-6.
1999: J A Alkemade; J H van Tongeren; U J van Haelst; A Smals; Peter M Steijlen; P C M van de Kerkhof
Delayed diagnosis of glucagonoma syndrome.
Clinical and experimental dermatology 1999;24(6):455-7.
1999: Peter M Steijlen; Maurice A M van Steensel
Paradominant inheritance, a hypothesis explaining occasional familial occurrence of sporadic syndromes.
American journal of medical genetics 1999;85(4):359-60.
1999: Maurice A M van Steensel; Frances J D Smith; Peter M Steijlen; Irma Kluijt; Howard P Stevens; AG Messenger; Hannie Kremer; M G Dunnill; C Kennedy; Colin S Munro; V R Doherty; John A McGrath; Seana P Covello; CM Coleman; Jouni Uitto; W H Irwin McLean
The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.
American journal of human genetics 1999;65(2):413-9.
1998: P C M van de Kerkhof; MJ de Rooij; Peter M Steijlen
Spontaneous course of hemangiomas: facts and speculations.
International journal of dermatology 1998;37(2):101-2.
1997: Carla Boetes; A P M Boll; P H Hartman; C G van Oostrom; Paul N M A Rieu; MJ de Rooij; Paul H M Spauwen; Peter M Steijlen
[Klippel-Trenaunay-type congenital angiodysplasia syndrome; medical and psychological aspects].
Nederlands tijdschrift voor geneeskunde 1997;141(13):650-1.
1997: G P Lucker; A M Heremans; P J Boegheim; P C M van de Kerkhof; Peter M Steijlen
Oral treatment of ichthyosis by the cytochrome P-450 inhibitor liarozole.
The British journal of dermatology 1997;136(1):71-5.