Comparison of Two Diagnostic Assays for Anti-Laminin 332 Mucous Membrane Pemphigoid von Goletz, Stephanie, Giurdanella, Federica, Holtsche, Maike M., Nijenhuis, Miranda, Horvath, Barbara, Diercks, Gilles F. H., Zillikens, Detlef, Hashimoto, Takashi, Schmidt, Enno, Pas, Hendri H.

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Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplex von Gostyńska, Katarzyna B, Nijenhuis, Miranda, Lemmink, Henny, Pas, Hendri H, Pasmooij, Anna M G, Lang, Kristin Kernland, Castañón, Maria J, Wiche, Gerhard, Jonkman, Marcel F

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Revertant Mosaicism Due to a Second-Site Mutation in COL7A1 in a Patient with Recessive Dystrophic Epidermolysis Bullosa von Pasmooij, Anna M.G., Garcia, Marta, Escamez, Maria J., Miranda Nijenhuis, A., Azon, Antoni, Cuadrado-Corrales, Natividad, Jonkman, Marcel F., Del Rio, Marcela

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Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy von Gostyński, Antoni, Llames, Sara, García, Marta, Escamez, María J., Martinez-Santamaria, Lucía, Nijenhuis, Miranda, Meana, Alvaro, Pas, Hendri H., Larcher, Fernando, Pasmooij, Anna M.G., Jonkman, Marcel F., Del Rio, Marcela

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Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands: Expansion of the mutation database and unusual phenotype–genotype correlations von van den Akker, Peter C, van Essen, Anthonie J, Kraak, Marian M.J, Meijer, Rowdy, Nijenhuis, Miranda, Meijer, Gonnie, Hofstra, Robert M.W, Pas, Hendri H, Scheffer, Hans, Jonkman, Marcel F

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The Autoimmune IgG Subclass Response Defines the IgG Deposition Pattern in Pemphigus Patient Skin von Pas, Hendri H., van der Molen, Marije, van Nijen-Vos, Laura, Nijenhuis, Miranda, Bremer, Jeroen

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Revertant Mosaicism in Epidermolysis Bullosa Caused by Mitotic Gene Conversion von Jonkman, Marcel F, Scheffer, Hans, Stulp, Rein, Pas, Hendri H, Nijenhuis, Miranda, Heeres, Klaas, Owaribe, Katsushi, Pulkkinen, Leena, Uitto, Jouni

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Two major 5′-untranslated regions for type XVII collagen mRNA von van Zalen, Sebastiaan, Nijenhuis, Miranda, Jonkman, Marcel F., Pas, Hendri H.

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Natural Gene Therapy May Occur in All Patients with Generalized Non-Herlitz Junctional Epidermolysis Bullosa with COL17A1 Mutations von Pasmooij, Anna M.G., Nijenhuis, Miranda, Brander, Renske, Jonkman, Marcel F.

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Disruption of TUFT1, a Desmosome-Associated Protein, Causes Skin Fragility, Woolly Hair, and Palmoplantar Keratoderma von Verkerk, Annemieke J M H, Andrei, Daniela, Vermeer, Mathilde C S C, Kramer, Duco, Schouten, Marloes, Arp, Pascal, Verlouw, Joost A M, Pas, Hendri H, Meijer, Hillegonda J, van der Molen, Marije, Oberdorf-Maass, Silke, Nijenhuis, Miranda, Romero-Herrera, Pedro H, Hoes, Martijn F, Bremer, Jeroen, Slotman, Johan A, van den Akker, Peter C, Diercks, Gilles F H, Giepmans, Ben N G, Stoop, Hans, Saris, Jasper J, van den Ouweland, Ans M W, Willemsen, Rob, Hublin, Jean-Jacques, Dean, M Christopher, Hoogeboom, A Jeannette M, Silljé, Herman H W, Uitterlinden, André G, van der Meer, Peter, Bolling, Maria C

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A PLEC Isoform Identified in Skin, Muscle, and Heart von Gostyńska, Katarzyna B., Lemmink, Henny, Bremer, Jeroen, Pas, Hendri H., Nijenhuis, Miranda, van den Akker, Peter C., Sinke, Richard J., Jonkman, Marcel F., Pasmooij, Anna M.G.

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Particle Bombardment of Ex Vivo Skin to Deliver DNA and Express Proteins von Sokol, Ena, Nijenhuis, Miranda, Sjollema, Klaas A., Jonkman, Marcel F., Pas, Hendri H., Giepmans, Ben N. G.

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Deletion of a Cytoplasmic Domain of Integrin β4 Causes Epidermolysis Bullosa Simplex1 von Jonkman, Marcel F., Pas, Hendri H., Nijenhuis, Miranda, Kloosterhuis, Guus, Steege, Gerrit van der

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Multiple Correcting COL17A1 Mutations in Patients with Revertant Mosaicism of Epidermolysis Bullosa von Pasmooij, Anna M.G., Pas, Hendri H., Deviaene, Franciska C.L., Nijenhuis, Miranda, Jonkman, Marcel F.

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Deletion of a Cytoplasmic Domain of Integrin β4 Causes Epidermolysis Bullosa Simplex von JONKMAN, Marcel F, PAS, Hendri H, NIJENHUIS, Miranda, KLOOSTERHUIS, Guns, VAN DER STEEGE, Gerrit

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Partial Revertant Mosaicism of Keratin 14 in a Patient with Recessive Epidermolysis Bullosa Simplex von SCHUILENGA-HUT, Petra H. L, SCHEFFER, Hans, PAS, Hendri H, NIJENHUIS, Miranda, BUYS, Charles H. C. M, JONKMAN, Marcel F

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Disruption of tuftelin 1, a desmosome associated protein, causes skin fragility, woolly hair and palmoplantar keratoderma von Verkerk, Annemieke JMH, Andrei, Daniela, Vermeer, Mathilde CSC, Kramer, Duco, Schouten, Marloes, Arp, Pascal, Verlouw, Joost AM, Pas, Hendri H, Meijer, Hillegonda J, van der Molen, Marije, Oberdorf-Maass, Silke, Nijenhuis, Miranda, Romero-Herrera, Pedro H, Hoes, Martijn F, Bremer, Jeroen, Slotman, Johan A, van den Akker, Peter C, Diercks, Gilles FH, Giepmans, Ben NG, Stoop, Hans, Saris, Jasper, van den Ouweland, Ans MW, Willemsen, Rob, Hublin, Jean-Jacques, Dean, M Christopher, Hoogeboom, A Jeannette M, Silljé, Herman HW, Uitterlinden, André G, van der Meer, Peter, Bolling, Maria C

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Deletion of a cytoplasmic domain of integrin beta4 causes epidermolysis bullosa simplex von Jonkman, Marcel F, Pas, Hendri H, Nijenhuis, Miranda, Kloosterhuis, Guus, Steege, Gerritvander

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Deletion of a Cytoplasmic Domain of Integrin [beta]4 Causes Epidermolysis Bullosa Simplex1 von Jonkman, Marcel F, Pas, Hendri H, Nijenhuis, Miranda, Kloosterhuis, Guus, van der Steege, Gerrit

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Natural Gene Therapy in Dystrophic Epidermolysis Bullosa von van den Akker, Peter C, Nijenhuis, Miranda, Meijer, Gonnie, Hofstra, Robert M. W, Jonkman, Marcel F, Pasmooij, Anna M. G

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