Epidermolysis Bullosa Simplex due to a Novel BPAG1-e Homozygous Pathogenic Variant Revealed by Bullous Scabies by Nathalie Pironon, Anne Welfringer-Morin, Stéphanie Leclerc-Mercier, Emmanuelle Bourrat, Alain Hovnanian

Subjects: “…Epidermolysis Bullosa Simplex…”
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Keratin-associated epidermolysis bullosa simplex: phenotypes and challenges in clinical trials – a narrative review and systematic update by Verena Wally, Tobias Welponer, Hans-Peter Wiesinger, Anja Diem, Konstantin Thiel, Martin Geroldinger, Georg Zimmermann, Julia I. Hummel, Sonja Dorfer, Josefina Piñón Hofbauer, Johann W. Bauer, Martin Laimer

Subjects: “…Epidermolysis bullosa simplex…”
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Impaired Autophagic Flux in Skeletal Muscle of Plectin‐Related Epidermolysis Bullosa Simplex With Muscular Dystrophy by Michaela M. Zrelski, Margret Eckhard, Petra Fichtinger, Sabrina Hösele, Andy Sombke, Leonid Mill, Monika Kustermann, Wolfgang M. Schmidt, Fiona Norwood, Ursula Schlötzer‐Schrehardt, Gerhard Wiche, Rolf Schröder, Lilli Winter

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Autosomal recessive epidermolysis bullosa simplex due to compound heterozygous mutations in <i>DST</i> gene: first Italian case and literature review by Andrea Diociaiuti, Ruggiero Davide Zingarelli, Dario Francesco D'Urso, Giovanna Zambruno, May El Hachem

Subjects: “…Autosomal recessive epidermolysis bullosa simplex…”
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