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Results: 1-22 |
Results: 22

Authors: van der Steege, G Schuilenga-Hut, PHL Buys, CHCM Scheffer, H Pas, HH Jonkman, MF
Citation: G. Van Der Steege et al., Persistent failures in gene repair, NAT BIOTECH, 19(4), 2001, pp. 305-306

Authors: Toth, GG Jonkman, MF
Citation: Gg. Toth et Mf. Jonkman, Therapy of pemphigus, CLIN DERMAT, 19(6), 2001, pp. 761-767

Authors: van der Meer, JB Schuttelaar, MLA Toth, GG Kardaun, SH Beerthuizen, G de Jong, MCJM Jonkman, MF Nieuwenhuis, P
Citation: Jb. Van Der Meer et al., Successful dexamethasone pulse therapy in a toxic epidermal necrolysis (TEN) patient featuring recurrent TEN to oxazepam, CLIN EXP D, 26(8), 2001, pp. 654-656

Authors: van Leusden, MR Pas, HH Gedde-Dahl, T Sonnenberg, A Jonkman, MF
Citation: Mr. Van Leusden et al., Truncated type XVII collagen expression in a patient with non-Herlitz junctional epidermolysis bullosa caused by a homozygous splice-site mutation, LAB INV, 81(6), 2001, pp. 887-894

Authors: Stouthamer, A Nieboer, C Van der Waal, RIF Jonkman, MF
Citation: A. Stouthamer et al., Normal expression of the 19-DEJ-1 epitope in two siblings with late-onset junctional epidermolysis bullosa, BR J DERM, 144(5), 2001, pp. 1054-1057

Authors: Van der Waal, RIF Van de Scheur, MR Pas, HH Jonkman, MF Van Groeningen, CJ Nieboer, C Starink, TM
Citation: Rif. Van Der Waal et al., Linear IgA bullous dermatosis in a patient with renal cell carcinoma, BR J DERM, 144(4), 2001, pp. 870-873

Authors: van der Waal, RIF Pas, HH Nousari, HC Schulten, EAJM Jonkman, MF Nieboer, C Stoof, TJ Starink, TM Anhalt, GJ
Citation: Rif. Van Der Waal et al., Paraneoplastic pemphigus caused by an epithelioid leiomyosarcoma and associated with fatal respiratory failure, ORAL ONCOL, 36(4), 2000, pp. 390-393

Authors: Molnar, K van der Steege, G Jonkman, MF Nijenhuis, M Husz, S van der Meer, JB Pas, HH
Citation: K. Molnar et al., Two type XVII collagen (BP180) mRNA transcripts in human keratinocytes: a long and a short form, CLIN EXP D, 25(1), 2000, pp. 71-76

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

Authors: Hut, PHL van der Vlies, P Jonkman, MF Verlind, E Shimizu, H Buys, CHCM Scheffer, H
Citation: Phl. Hut et al., Exempting homologous pseudogene sequences from polymerase chain reaction amplification allows genomic keratin 14 hotspot mutation analysis, J INVES DER, 114(4), 2000, pp. 616-619

Authors: Zillikens, D Ishiko, A Jonkman, MF Chimanovitch, I Shimizu, H Hashimoto, T Brocker, EB
Citation: D. Zillikens et al., Autoantibodies in anti-p200 pemphigoid stain skin lacking laminin 5 and type VII collagen, BR J DERM, 143(5), 2000, pp. 1043-1049

Authors: Jonkman, MF Schuur, J Dijk, F Heeres, K de Jong, MCJM van der Meer, JB Yancey, KB Pas, HH
Citation: Mf. Jonkman et al., Inflammatory variant of epidermolysis bullosa acquisita with IgG autoantibodies against type VII collagen and laminin alpha 3, ARCH DERMAT, 136(2), 2000, pp. 227-231

Authors: Jonkman, MF
Citation: Mf. Jonkman, Hereditary skin diseases of hemidesmosomes, J DERMA SCI, 20(2), 1999, pp. 103-121

Authors: Toth, GG Kloosterman, C Uges, DRA Jonkman, MF
Citation: Gg. Toth et al., Pharmacokinetics of high-dose oral and intravenous dexamethasone, THER DRUG M, 21(5), 1999, pp. 532-535

Authors: Moog, U de Die-Smulders, CEM Scheffer, H van der Vlies, P Henquet, CJM Jonkman, MF
Citation: U. Moog et al., Epidermolysis bullosa simplex with mottled pigmentation: Clinical aspects and confirmation of the P24L mutation in the KRT5 gene in further patients, AM J MED G, 86(4), 1999, pp. 376-379

Authors: Jonkman, MF
Citation: Mf. Jonkman, Revertant mosaicism in human genetic disorders, AM J MED G, 85(4), 1999, pp. 361-364

Authors: Jonkman, MF Moreno, G Rouan, F Oranje, AP Pulkkinen, L Uitto, J
Citation: Mf. Jonkman et al., Dominant dystrophic epidermolysis bullosa (Pasini) caused by a novel glycine substitution mutation in the type VII collagen gene (COL7A1), J INVES DER, 112(5), 1999, pp. 815-817

Authors: Pas, HH Kloosterhuis, GJ Nijenhuis, M de Jong, MCJM van der Meer, JB Jonkman, MF
Citation: Hh. Pas et al., Type XVII collagen (BP180) and LAD-1 are present as separate trimeric complexes, J INVES DER, 112(1), 1999, pp. 58-61

Authors: Van der Wal, VB Vader, PCV Mandema, JM Jonkman, MF
Citation: Vb. Van Der Wal et al., Crusted (Norwegian) scabies in a patient with dystrophic epidermolysis bullosa, BR J DERM, 141(5), 1999, pp. 918-921

Authors: Toth, GG Jonkman, MF
Citation: Gg. Toth et Mf. Jonkman, Successful treatment of recalcitrant penicillamine-induced pemphigus foliaceus by low-dose intravenous immunoglobulins, BR J DERM, 141(3), 1999, pp. 583-585

Authors: van der Waal, RIF Pas, HH Anhalt, GJ Schulten, EAJM Jonkman, MF Nieboer, C
Citation: Rif. Van Der Waal et al., Paraneoplastic pemphigus as the presenting symptom of a lymphoma of the tongue, ORAL ONCOL, 34(6), 1998, pp. 567-570

Authors: Rouan, F Pulkkinen, L Jonkman, MF Bauer, JW Cserhalmi-Friedman, PB Christiano, AM Uitto, J
Citation: F. Rouan et al., Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: Implications for geneticcounseling, J INVES DER, 111(6), 1998, pp. 1210-1213
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