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Results: 1-13 |
Results: 13
Large melanocytic nevi in hereditary epidermolysis bullosa
Authors: Bauer, JW Schaeppi, H Kaserer, C Hantich, B Hintner, H
Citation: Jw. Bauer et al., Large melanocytic nevi in hereditary epidermolysis bullosa, J AM ACAD D, 44(4), 2001, pp. 577-584
Pathogenesis of the permeability barrier abnormality in epidermolytic hyperkeratosis
Authors: Schmuth, M Yosipovitch, G Williams, ML Weber, F Hintner, H Ortiz-Urda, S Rappersberger, K Crumrine, D Feingold, KR Elias, PM
Citation: M. Schmuth et al., Pathogenesis of the permeability barrier abnormality in epidermolytic hyperkeratosis, J INVES DER, 117(4), 2001, pp. 837-847
Is screening of the candidate gene necessary in unrelated partners of members of families with Herlitz junctional epidermolysis bullosa?
Authors: Klausegger, A Pulkkinen, L Pohla-Gubo, G Dallinger, G Puttinger, R Uitto, J Hintner, H Bauer, JW
Citation: A. Klausegger et al., Is screening of the candidate gene necessary in unrelated partners of members of families with Herlitz junctional epidermolysis bullosa?, J INVES DER, 116(3), 2001, pp. 474-475
A localized variant of paraneoplastic pemphigus: acantholysis associated with malignant melanoma
Authors: Schaeppi, H Bauer, JW Hametner, R Metze, D Ortiz-Urda, S Salmhofer, W Rappersberger, K Hintner, H
Citation: H. Schaeppi et al., A localized variant of paraneoplastic pemphigus: acantholysis associated with malignant melanoma, BR J DERM, 144(6), 2001, pp. 1249-1254
Human papillomavirus infection in Netherton's syndrome
Authors: Weber, F Fuchs, PG Pfister, HJ Hintner, H Fritsch, P Hoepfl, R
Citation: F. Weber et al., Human papillomavirus infection in Netherton's syndrome, BR J DERM, 144(5), 2001, pp. 1044-1049
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiency
Authors: Bauer, JW Rouan, F Kofler, B Rezniczek, GA Kornacker, I Muss, W Hametner, R Klausegger, A Huber, A Pohla-Gubo, G Wiche, G Uitto, J Hintner, H
Citation: Jw. Bauer et al., A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiency, AM J PATH, 158(2), 2001, pp. 617-625
Squamous cell carcinoma in junctional and dystrophic epidermolysis bullosa
Authors: Weber, F Bauer, JW Sepp, N Hogler, W Salmhofer, W Hintner, H Fritsch, P
Citation: F. Weber et al., Squamous cell carcinoma in junctional and dystrophic epidermolysis bullosa, ACT DER-VEN, 81(3), 2001, pp. 189-192
Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa
Authors: Fine, JD Eady, RAJ Bauer, EA Briggaman, RA Bruckner-Tuderman, L Christiano, A Heagerty, A Hintner, H Jonkman, MF McGrath, J McGuire, J Moshell, A Shimizu, H Tadini, G Uitto, J
Citation: Jd. Fine et al., Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa, J AM ACAD D, 42(6), 2000, pp. 1051-1066
Clinical testing of recombinant allergens of the mold Alternaria alternata
Authors: Unger, A Stoger, P Simon-Nobbe, B Susani, M Crameri, R Ebner, C Hintner, H Breitenbach, M
Citation: A. Unger et al., Clinical testing of recombinant allergens of the mold Alternaria alternata, INT A AL IM, 118(2-4), 1999, pp. 220-221
Revertant mosaicism: partial correction of a germ-line mutation in COL17A1by a frame-restoring mutation
Authors: Darling, TN Yee, C Bauer, JW Hintner, H Yancey, KB
Citation: Tn. Darling et al., Revertant mosaicism: partial correction of a germ-line mutation in COL17A1by a frame-restoring mutation, J CLIN INV, 103(10), 1999, pp. 1371-1377
Acatalasemia - Takahara's disease
Authors: Perner, H Krenkel, C Lackner, B Hintner, H Hawranek, T
Citation: H. Perner et al., Acatalasemia - Takahara's disease, HAUTARZT, 50(8), 1999, pp. 590-592
Prenatal diagnosis of recessive dystrophic epidermolysis bullosa in a family at risk for recurrence by haplotype analysis of the type VII collagen gene
Authors: Bauer, JW Ortiz, S Hengstschlager, M Pulkkinen, L Uitto, J Hintner, H Rappersberger, K
Citation: Jw. Bauer et al., Prenatal diagnosis of recessive dystrophic epidermolysis bullosa in a family at risk for recurrence by haplotype analysis of the type VII collagen gene, HAUTARZT, 50(2), 1999, pp. 121-126
Ocular involvement in IgA-epidermolysis bullosa acquisita
Authors: Bauer, JW Schaeppi, H Metze, D Muss, W Pohla-Gubo, G Hametner, R Ruckhofer, J Grabner, G Hintner, H
Citation: Jw. Bauer et al., Ocular involvement in IgA-epidermolysis bullosa acquisita, BR J DERM, 141(5), 1999, pp. 887-892
Risultati: 1-13 |