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    1. Glade, C; van Steensel, MAM; Steijlen, PM
      Hypotrichosis, lymphedema of the legs and acral telangiectasias - new syndrome?

      EUROPEAN JOURNAL OF DERMATOLOGY
    2. van Steensel, MAM; van Geel, M; Steijlen, PM
      The molecular basis of hair growth

      EUROPEAN JOURNAL OF DERMATOLOGY
    3. van Steensel, MAM; Smith, FJD; Steijlen, PM
      A new type of pachyonychia congenita

      EUROPEAN JOURNAL OF DERMATOLOGY
    4. Haenen, JH; Wollersheim, H; Janssen, MCH; Van 't Hof, MA; Steijlen, PM; van Langen, H; Skotnicki, SH; Thien, T
      Evolution of deep venous thrombosis: A 2-year follow-up using duplex ultrasound scan and strain-gauge plethysmography

      JOURNAL OF VASCULAR SURGERY
    5. Willemsen, MAAP; Lutt, MAJ; Steijlen, PM; Cruysberg, JRM; van der Graaf, M; Nijhuis-van der Sanden, MWG; Pasman, JW; Mayatepek, E; Rotteveel, JJ
      Clinical and biochemical effects of zileuton in patients with the Sjogren-Larsson syndrome

      EUROPEAN JOURNAL OF PEDIATRICS
    6. Schalkwijk, J; Zweers, MC; Steijlen, PM; Dean, WB; Taylor, G; van Vlijmen, IM; van Haren, B; Miller, WL; Bristow, J
      A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.

      NEW ENGLAND JOURNAL OF MEDICINE
    7. van Steensel, MAM; Koedam, MI; Swinkels, OQ; Rietveld, F; Steijlen, PM
      Woolly hair, premature loss of teeth, nail dystrophy, acral hyperkeratosisand facial abnormalities: possible new syndrome in a Dutch kindred

      BRITISH JOURNAL OF DERMATOLOGY
    8. Van Steensel, MAM; Jaspers, NGJ; Steijlen, PM
      A case of Rombo syndrome

      BRITISH JOURNAL OF DERMATOLOGY
    9. Willemsen, MAAP; Ijlst, L; Steijlen, PM; Rotteveel, JJ; de Jong, JGN; van Domburg, PHMF; Mayatepek, E; Gabreels, FJM; Wanders, RJA
      Clinical, biochemical and molecular genetic characteristics of 19 patientswith the Sjogren-Larsson syndrome

      BRAIN
    10. Steijlen, PM; Vietor, HE; van Steensel, MAM; Happle, R
      Sweat testing in hypomelanosis of Ito: divergent results reflecting genetic heterogeneity

      EUROPEAN JOURNAL OF DERMATOLOGY
    11. van den Berg, JSP; Hennekam, RCM; Cruysberg, JRM; Steijlen, PM; Swart, J; Tijmes, N; Limburg, M
      Prevalence of symptomatic intracranial aneurysm and ischaemic stroke in pseudoxanthoma elasticum

      CEREBROVASCULAR DISEASES
    12. Wijnberg, DS; Deutman, HC; Steijlen, PM; Spauwen, PHM
      CO2 laser treatment of benign juvenile acanthosis nigricans

      EUROPEAN JOURNAL OF PLASTIC SURGERY
    13. Willemsen, MAAP; Rotteveel, JJ; Steijlen, PM; Heerschap, A; Mayatepek, E
      5-lipoxygenase inhibition: A new treatment strategy for Sjogren-Larsson syndrome

      NEUROPEDIATRICS
    14. van Steensel, MAM; Happle, R; Steijlen, PM
      Molecular genetics of the hair follicle: The state of the art

      PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE
    15. Gerritsen, MJP; Steijlen, PM; Brunner, HG; Rieu, P
      Cutis marmorata telangiectatica congenita: report of 18 cases

      BRITISH JOURNAL OF DERMATOLOGY
    16. van Doorn, R; Van Haselen, CW; Vader, PCV; Geerts, ML; Heule, F; de Rie, M; Steijlen, PM; Dekker, SK; van Vloten, WA; Willemze, R
      Mycosis fungoides - Disease evolution and prognosis of 309 Dutch patients

      ARCHIVES OF DERMATOLOGY
    17. Steijlen, PM; van de Kerkhof, PCM
      Vitamin D analogs in ichthyosis and other disorders of keratinization

      VITAMIN D IN DERMATOLOGY
    18. Willemsen, MAAP; Rotteveel, JJ; Steijlen, PM; Wanders, RJA
      Incomplete Sjogren-Larsson syndrome in two Japanese siblings?

      DERMATOLOGY
    19. Ruiz-Perez, VL; Carter, SA; Healy, E; Todd, C; Rees, JL; Steijlen, PM; Carmichael, AJ; Lewis, HM; Hohl, D; Itin, P; Vahlquist, A; Gobello, T; Mazzanti, C; Reggazini, R; Nagy, G; Munro, CS; Strachan, T
      ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class

      HUMAN MOLECULAR GENETICS
    20. Alkemade, JAC; van Tongeren, JHM; van Haelst, UJGM; Smals, A; Steijlen, PM; van de Kerkhof, PCM
      Delayed diagnosis of glucagonoma syndrome

      CLINICAL AND EXPERIMENTAL DERMATOLOGY
    21. Bousema, MT; Kramer, MHH; Steijlen, PM
      Extensive capillary malformation with a compensated coagulopathy

      CLINICAL AND EXPERIMENTAL DERMATOLOGY
    22. Steijlen, PM; van Steensel, MAM
      Paradominant inheritance, a hypothesis explaining occasional familial occurrence of sporadic syndromes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    23. van Domburg, PHMF; Willemsen, MAAP; Rotteveel, JJ; de Jong, JGN; Thijssen, HOM; Heerschap, A; Cruysberg, JRM; Wanders, RJA; Gabreels, FJM; Steijlen, PM
      Sjogren-Larsson syndrome - Clinical and MRI/MRS findings in FALDH-deficient patients

      NEUROLOGY
    24. Willemsen, MAAP; Steijlen, PM; de Jong, JGN; Rotteveel, JJ; Ijlst, L; van Werkhoven, MA; Wanders, RJA
      A novel 4 bp deletion mutation in the FALDH gene segregating in a Turkish family with Sjogren-Larsson syndrome

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    25. Smith, FJD; Del Monaco, M; Steijlen, PM; Munro, CS; Morvay, M; Coleman, CM; Rietveld, FJR; Uitto, J; McLean, WH
      Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1

      BRITISH JOURNAL OF DERMATOLOGY
    26. van Steensel, M; Smith, FJD; Steijlen, PM; Kluijt, I; Stevens, HP; Messenger, A; Kremer, H; Dunnill, MGS; Kennedy, C; Munro, CS; Doherty, VR; McGrath, JA; Covello, SP; Coleman, CM; Uitto, J; McLean, WHI
      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
    27. van Steensel, MAM; Steijlen, PM
      Hypomelanosis of Ito: A symptom, not a syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    28. SMITH R; HEALY E; SIDDIQUI S; FLANAGAN N; STEIJLEN PM; ROSDAHL I; JACQUES JP; ROGERS S; TURNER R; JACKSON IJ; BIRCHMACHIN MA; REES JL
      MELANOCORTIN-1 RECEPTOR VARIANTS IN AN IRISH POPULATION

      Journal of investigative dermatology
    29. SMITH FJD; STEIJLEN PM; MCKENNA K; HEALY E; REES JL; FISHER MP; BONIFAS JM; EPSTEIN EH; MCKUSICK VA; TAN E; UITTO J; MCLEAN WHI
      CLONING OF MULTIPLE K16 GENES AND GENOTYPE-PHENOTYPE CORRELATION IN PACHYONYCHIA-CONGENITA TYPE-I AND FOCAL PPK

      Journal of investigative dermatology
    30. Kremer, H; Lavrijsen, APM; McLean, WHI; Lane, EB; Melchers, D; Ruiter, DJ; Mariman, ECM; Steijlen, PM
      An atypical form of bullous congenital ichthyosiform erythroderma is caused by a mutation in the L12 linker region of keratin 1

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    31. VANDEKERKHOF PCM; DEROOIJ M; STEIJLEN PM
      SPONTANEOUS COURSE OF HEMANGIOMAS - FACTS AND SPECULATIONS

      International journal of dermatology
    32. HAMEL BCJ; PALS G; ENGELS CHAM; VANDENAKKER E; BOERS GHJ; VANDONGEN PWJ; STEIJLEN PM
      EHLERS-DANLOS-SYNDROME AND TYPE-III COLLAGEN ABNORMALITIES - A VARIABLE CLINICAL SPECTRUM

      Clinical genetics
    33. SMITT JHS; VANASPEREN CJ; NIESSEN CM; BEEMER FA; VANESSEN AJ; HULSMANS RFHJ; ORANJE AP; STEIJLEN PM; WESBYVANSWAAY E; TAMMINGA P; BRESLAUSIDERIUS EJ
      RESTRICTIVE DERMOPATHY - REPORT OF 12 CASES

      Archives of dermatology
    34. LUCKER GPH; ZEEDIJK N; STEIJLEN PM
      THE HURIEZ-SYNDROME - SCLEROATROPHIC PALMOPLANTAR KERATODERMA

      EJD. European journal of dermatology
    35. GERRITSEN MJP; VANDEKERKHOF PCM; VANVLIJMENWILLEMS IMJJ; STEIJLEN PM
      EXPRESSION OF FILAGGRIN, INVOLUCRIN AND TENASCIN IN MONOGENIC DISORDERS OF KERATINIZATION

      EJD. European journal of dermatology
    36. FISCHER J; BLANCHETBARDON C; PRUDHOMME JF; PAVEK S; STEIJLEN PM; DUBERTRET L; WEISSENBACH J
      MAPPING OF PAPILLON-LEFEVRE-SYNDROME TO THE CHROMOSOME 11Q14 REGION

      European journal of human genetics
    37. VANSTEENSEL MAM; STEIJLEN PM
      GENETICS OF PSORIASIS

      Clinics in dermatology
    38. VANSTEENSEL MAM; STEIJLEN PM; REES JL
      MOLECULAR-GENETIC APPROACHES TO SKIN-DISEASE - KERATINS AND KERATINIZATION

      Journal of the Royal College of Physicians of London
    39. LUCKER GPH; HEREMANS AMC; BOEGHEIM PJ; VANDEKERKHOF PCM; STEIJLEN PM
      ORAL TREATMENT OF ICHTHYOSIS BY THE CYTOCHROME-P-450 INHIBITOR LIAROZOLE

      British journal of dermatology
    40. HAPPLE R; STEIJLEN PM; THEILE U; KARITZKY D; TINSCHERT S; ALBRECHTNEBE H; KUSTER W
      PATCHY DERMAL HYPOPLASIA AS A CHARACTERISTIC FEATURE OF PROTEUS SYNDROME

      Archives of dermatology
    41. LENZNER U; HAPPLE R; KREMER H; MENSING H; REINEL D; STEIJLEN PM; ULRICH R
      ICHTHYOSIS BULLOSA OF SIEMENS - A DISTINCT TYPE OF EPIDERMOLYTIC HYPERKERATOSIS

      EJD. European journal of dermatology
    42. RAMPEN FHJ; STEIJLEN PM
      DIPHENCYPRONE IN THE MANAGEMENT OF REFRACTORY PALMOPLANTAR AND PERIUNGUAL WARTS - AN OPEN STUDY

      Dermatology
    43. VANDEKERKHOF PCM; VANPELT H; LUCKER GPH; STEIJLEN PM; HEREMANS A
      TOPICAL R-85355, A POTENT AND SELECTIVE 5-LIPOXYGENASE INHIBITOR, FAILS TO IMPROVE PSORIASIS

      Skin pharmacology
    44. LUCKER GPH; VANDEKERKHOF PCM; CASTELIJNS FACM; STEIJLEN PM
      TOPICAL TREATMENT OF DARIERS-DISEASE WITH 13-CIS-RETINOIC ACID - A CLINICAL AND IMMUNOHISTOCHEMICAL STUDY

      Journal of dermatological treatment
    45. OOSTENBRINK JH; COHEN EB; STEIJLEN PM; VANDEKERKHOF PCM
      ORAL-CONTRACEPTIVES IN THE TREATMENT OF DARIER-WHITE-DISEASE - A CASE-REPORT AND REVIEW OF THE LITERATURE

      Clinical and experimental dermatology
    46. FEINDKOOPMANS A; VANDERVALK PGM; STEIJLEN PM; VANDEKERKHOF PCM
      TOXIC PUSTULODERMA ASSOCIATED WITH CLEMASTINE THERAPY

      Clinical and experimental dermatology
    47. HOFSTRA RMW; SIJMONS RH; STELWAGEN T; STULP RP; KOUSSEFF BG; LIPS CJM; STEIJLEN PM; VANVOORSTVADER PC; BUYS CHCM
      RET MUTATION SCREENING IN FAMILIAL CUTANEOUS LICHEN AMYLOIDOSIS AND IN SKIN AMYLOIDOSIS ASSOCIATED WITH MULTIPLE ENDOCRINE NEOPLASIA

      Journal of investigative dermatology
    48. LUCKER GPH; STEIJLEN PM
      KERATOSIS PALMOPLANTARIS VARIANS ET PUNCT ATA - CLINICAL VARIABILITY OF A SINGLE GENETIC-DEFECT

      Hautarzt
    49. VANDERKERKHOF PCM; STEIJLEN PM; RAYMAKERS RAP
      ACRODERMATITIS CONTINUA OF HALLOPEAU IN A PATIENT WITH MYELODYSPLASTIC SYNDROME

      British journal of dermatology
    50. JONKMAN MF; DEJONG MCJM; HEERES K; STEIJLEN PM; OWARIBE K; KUSTER W; MEURER M; GEDDEDAHL T; SONNENBERG A; BRUCKNERTUDERMAN L
      GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA - EITHER 180-KD BULLOUS PEMPHIGOID ANTIGEN OR LAMININ-5 DEFICIENCY

      Archives of dermatology
    51. LUCKER GPH; STEIJLEN PM; SUYKERBUYK EJA; KRAGBALLE K; BRANDRUP F; VANDEKERKHOF PCM
      FLOW-CYTOMETRIC INVESTIGATION OF EPIDERMAL-CELL CHARACTERISTICS IN MONOGENIC DISORDERS OF KERATINIZATION AND THEIR MODULATION BY TOPICAL CALCIPOTRIOL TREATMENT

      Acta dermato-venereologica
    52. VANDERVLEUTEN CJM; GERRITSEN MJP; STEIJLEN PM; DEJONG EMGJ; VANDEKERKHOF PCM
      A THERAPEUTIC APPROACH TO ERYTHRODERMIC PSORIASIS - REPORT OF A CASE AND A DISCUSSION OF THERAPEUTIC OPTIONS

      Acta dermato-venereologica
    53. LUCKER GPH; VANDEKERKHOF PCM; CASTELIJNS FACM; VANDIJK MR; SCHALKWIJK LJM; STEIJLEN PM
      TOPICAL TREATMENT OF ICHTHYOSES WITH 13-CIS RETINOIC ACID - A CLINICAL AND IMMUNOHISTOCHEMICAL STUDY

      EJD. European journal of dermatology
    54. VANDEKERKHOF PCM; STEIJLEN PM
      IGA DEFICIENCY AND PSORIASIS RELEVANCE OF IGA IN THE PATHOGENESIS OF PSORIASIS

      Dermatology
    55. LUCKER GPH; VANDEKERKHOF PCM; CRUYSBERG JRM; DERKINDEREN DJ; STEIJLEN PM
      TOPICAL TREATMENT OF SJOGREN-LARSSON SYNDROME WITH CALCIPOTRIOL

      Dermatology
    56. LUCKER GPH; STEIJLEN PM
      PACHYONYCHIA-CONGENITA TARDA

      Clinical and experimental dermatology
    57. ARNOLD WP; MERKX MAW; STEIJLEN PM
      VARIANT OF ODONTOONYCHODERMAL DYSPLASIA

      American journal of medical genetics
    58. JONKMAN MF; SCHEFFER H; SONNENBERG A; HEERES K; STEIJLEN PM; OWARIBE K; GEDDEDAHL T; KUSTER W; MEURER M; BRUCKNERTUDERMAN L
      GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA - EITHER 180-KD BULLOUS PEMPHIGOID ANTIGEN (BP180) OR LAMININ-5 IS DEFICIENT

      Journal of investigative dermatology
    59. MELCHERS D; KREMER H; BICHAKJIAN CK; STEIJLEN PM
      MUTATION ANALYSIS IN PATIENTS WITH BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA OF BROCQ

      Journal of investigative dermatology
    60. LUCKER GPH; HEREMANS A; BOEGHEIM JPJ; STEIJLEN PM
      TOPICAL LIAROZOLE TREATMENT OF ICHTHYOSIS - A DOUBLE-BLIND BILATERALLY PAIRED, CLINICAL AND IMMUNOHISTOCHEMICAL STUDY

      Journal of investigative dermatology
    61. EVERS MEJW; STEIJLEN PM; HAMEL BCJ
      APLASIA-CUTIS-CONGENITA AND ASSOCIATED DISORDERS - AN UPDATE

      Clinical genetics
    62. LUCKER GPH; STEIJLEN PM
      ACROKERATOSIS PARANEOPLASTICA (BAZEX SYNDROME) OCCURRING WITH ACQUIRED ICHTHYOSIS IN HODGKINS-DISEASE

      British journal of dermatology
    63. LUCKER GPH; STEIJLEN PM; VANDEKERKHOF PCM
      EFFECT OF TOPICAL CALCIPOTRIOL ON CONGENITAL ICHTHYOSES

      British journal of dermatology
    64. LUCKER GPH; HAPPLE R; STEIJLEN PM
      AN UNUSUAL CASE OF POROKERATOSIS INVOLVING THE NATAL CLEFT - POROKERATOSIS PTYCHOTROPICA

      British journal of dermatology
    65. KRAGBALLE K; STEIJLEN PM; IBSEN HH; VANDEKERKHOF PCM; ESMANN J; SORENSEN LH; AXELSEN MB
      EFFICACY, TOLERABILITY, AND SAFETY OF CALCIPOTRIOL OINTMENT IN DISORDERS OF KERATINIZATION - RESULTS OF A RANDOMIZED, DOUBLE-BLIND, VEHICLE-CONTROLLED, RIGHT-LEFT COMPARATIVE-STUDY

      Archives of dermatology
    66. LUCKER GPH; STEIJLEN PM
      THE COEXISTENCE OF LINEAR AND GIANT POROKERATOSIS ASSOCIATED WITH BOWENS-DISEASE

      Dermatology
    67. LUCKER GPH; STEIJLEN PM
      WIDESPREAD LEUCOKERATOSIS IN NOONANS-SYNDROME

      Clinical and experimental dermatology
    68. LUCKER GPH; STEIJLEN PM
      THE OLMSTED-SYNDROME - MUTILATING PALMOPLANTAR AND PERIORIFICIAL KERATODERMA

      Journal of the American Academy of Dermatology
    69. CHANG A; LUCKER GPH; VANDEKERKHOF PCM; STEIJLEN PM
      PACHYONYCHIA-CONGENITA IN THE ABSENCE OF OTHER SYNDROME ABNORMALITIES

      Journal of the American Academy of Dermatology
    70. STEIJLEN PM; NEUMANN HAM; DERKINDEREN DJ; SMEETS DFCM; VANDERKERKHOF PCM; HAPPLE R
      CONGENITAL ATRICHIA, PALMOPLANTAR HYPERKERATOSIS, MENTAL-RETARDATION,AND EARLY LOSS OF TEETH IN 4 SIBLINGS - A NEW SYNDROME

      Journal of the American Academy of Dermatology
    71. STEIJLEN PM; KREMER H; VAKILZADEH F; HAPPLE R; LAVRIJSEN APM; ROPERS HH; MARIMAN ECM
      GENETIC-LINKAGE OF THE KERATIN TYPE-II GENE-CLUSTER WITH ICHTHYOSIS BULLOSA OF SIEMENS AND WITH AUTOSOMAL-DOMINANT ICHTHYOSIS EXFOLIATIVA

      Journal of investigative dermatology
    72. KREMER H; ZEEUWEN P; MCLEAN WHI; MARIMAN ECM; LANE EB; VANDEKERKHOF PCM; ROPERS HH; STEIJLEN PM
      ICHTHYOSIS BULLOSA OF SIEMENS IS CAUSED BY MUTATIONS IN THE KERATIN 2E GENE

      Journal of investigative dermatology
    73. KREMER H; ZEEUWEN P; MCLEAN WHI; MARIMAN ECM; LANE EB; VANDEKERKHOF PCM; ROPERS HH; STEIJLEN PM
      ICHTHYOSIS BULLOSA OF SIEMENS IS CAUSED BY MUTATIONS IN THE KERATIN 2E GENE

      Journal of investigative dermatology
    74. LUCKER GPH; STEIJLEN PM
      ORAL LIAROZOLE TREATMENT OF HEREDITARY ICHTHYOSES - A CLINICAL AND IMMUNOHISTOCHEMICAL STUDY

      Journal of investigative dermatology
    75. LUCKER GPH; VANDEKERKHOF PCM; VANDIJK MR; STEIJLEN PM
      EFFECT OF TOPICAL CALCIPOTRIOL ON CONGENITAL ICHTHYOSES

      British journal of dermatology
    76. LUCKER GPH; VANDEKERKHOF PCM; STEIJLEN PM
      THE HEREDITARY PALMOPLANTAR KERATOSES - AN UPDATED REVIEW AND CLASSIFICATION

      British journal of dermatology
    77. LUCKER GPH; KOOPMAN RJJ; STEIJLEN PM; VALK PGM
      TREATMENT OF PALMOPLANTAR LICHEN NITIDUS WITH ACITRETIN

      British journal of dermatology
    78. STEIJLEN PM; MAESSEN E; KRESSE H; VANVLIJMEN IMJJ; VERSTRAETEN AA; TRAUPE H; SCHALKWIJK J
      EXPRESSION OF TENASCIN, BIGLYCAN AND DECORIN IN DISORDERS OF KERATINIZATION

      British journal of dermatology
    79. VANDEKERKHOF PCM; STEIJLEN PM
      TOPICAL TREATMENT OF PITYRIASIS-RUBRA-PILARIS WITH CALCIPOTRIOL

      British journal of dermatology
    80. LUCKER GPH; VANDEKERKHOF PCM; STEIJLEN PM
      TOPICAL CALCIPOTRIOL IN THE TREATMENT OF EPIDERMOLYTIC PALMOPLANTAR KERATODERMA OF VORNER

      British journal of dermatology
    81. STEIJLEN PM; VANDEKERKHOF PCM
      TOPICAL TREATMENT OF MONOGENIC DISORDERS OF KERATINIZATION

      British journal of dermatology
    82. STEIJLEN PM; VANDOORENGREEBE RJ; VANDEKERKHOF PCM
      ACITRETIN IN THE TREATMENT OF LAMELLAR ICHTHYOSIS

      British journal of dermatology
    83. BARTSTRA HLJ; HULSMANS RFHJ; STEIJLEN PM; RUIGE M; DEDIESMULDERS CEM; CASSIMAN JJ
      MOSAIC EXPRESSION OF HYPOHIDROTIC ECTODERMAL DYSPLASIA IN AN ISOLATEDAFFECTED FEMALE CHILD

      Archives of dermatology
    84. STEIJLEN PM; REIFENSCHWEILER DOH; RAMAEKERS FCS; VANMUIJEN GNP; HAPPLE R; LINK M; RUITER DJ; VANDEKERKHOF PCM
      TOPICAL TREATMENT OF ICHTHYOSES AND DARIERS DISEASE WITH 13-CIS-RETINOIC ACID - A CLINICAL AND IMMUNOHISTOCHEMICAL STUDY

      Archives of dermatological research
    85. BRUNNER HG; HULSEBOS T; STEIJLEN PM; DERKINDEREN DJ; VANDERSTEEN A; HAMEL BCJ
      EXCLUSION OF THE NEUROFIBROMATOSIS 1 LOCUS IN A FAMILY WITH INHERITEDCAFE-AU-LAIT SPOTS

      American journal of medical genetics
    86. DEMARE S; KOOPMAN RJJ; STEIJLEN PM
      ACQUIRED PERFORATING DERMATOSIS (KYRLES-DISEASE)

      British journal of dermatology
    87. VANGERWEN HJL; KOOPMAN RJJ; STEIJLEN PM; HAPPLE R
      BECKERS NEVUS WITH LOCALIZED LIPOATROPHY AND IPSILATERAL BREAST HYPOPLASIA

      British journal of dermatology
    88. KINDEREN DJD; CRUYSBERG JRM; STEIJLEN PM
      SJOGREN-LARSSON SYNDROME

      British journal of dermatology
    89. ARNOLD WP; STEIJLEN PM; HAPPLE R
      FOCAL DERMAL HYPOPLASIA (GOLTZ-GORLIN SYNDROME)

      British journal of dermatology
    90. VANDEKERKHOF PCM; STEIJLEN PM; HAPPLE R
      COOCCURRENCE OF LINEAR PSORIASIS AND POROKERATOTIC ECCRINE OSTIAL ANDDERMAL DUCT NEVUS

      Acta dermato-venereologica


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Documento generato il 25/05/20 alle ore 04:57:35