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Seltene Varianten der Pemphigoiderkrankungen
Pemphigoid diseases comprise a heterogeneous group of subepidermal autoimmune blistering dermatoses characterized by autoantibodies against...
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A Review Comparing International Guidelines for the Management of Bullous Pemphigoid, Pemphigoid Gestationis, Mucous Membrane Pemphigoid, and Epidermolysis Bullosa Acquisita
Autoimmune blistering disease management can be challenging as treatment modalities vary greatly and no single standard of care exists. We...
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Thymosin β4: potential to treat epidermolysis bullosa and other severe dermal injuries
Thymosin β4 is a naturally-occurring regenerative protein present in almost all cells and body fluids, including wound fluid. In multiple preclinical...
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Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa
BackgroundEpidermolysis bullosa (EB) comprises inherited mechanobullous dermatoses with considerable morbidity and mortality. While current...
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A novel mutation in ITGB4 gene in a newborn with epidermolysis bullosa, pyloric atresia, and aplasia cutis congenita
BackgroundEpidermolysis bullosa with pyloric atresia (EB-PA), also known as Carmi syndrome, is an uncommon, autosomal recessive genodermatosis that...
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Spontaneous autoimmune subepidermal blistering diseases in animals: a comprehensive review
Autoimmune subepidermal blistering diseases (AISBDs) are rare skin disorders of animals that were first identified in dogs but several AISBDs are now...
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The Need of Differential Diagnosis Between Vulvar Lichen Sclerosus and Autoimmune Dermatoses in Adolescent Girls
IntroductionVulvar lichen sclerosus (VLS) is a chronic inflammatory condition affecting the anogenital region, which can manifest in prepubertal or...
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Dental implants in patients with epidermolysis bullosa: a systematic review
PurposeTo integrate the available data published on patients with epidermolysis bullosa (EB) rehabilitated with dental implants, as well as to review...
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Verbandsmaterial bei Kindern mit Epidermolysis bullosa
BackgroundEpidermolysis bullosa (EB) is a rare genetic disease that soon becomes apparent after a child’s birth. Mechanical stress in particular...
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EGFR inhibition for metastasized cutaneous squamous cell carcinoma in dystrophic epidermolysis bullosa
Dystrophic epidermolysis bullosa (DEB) is a hereditary skin fragility disorder, characterized by trauma-induced blistering followed by soft tissue...
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Esophageal dilation with EsoFLIP is faster than CRE balloon dilation combined with EndoFLIP in children
BackgroundControlled radial expansion (CRE) balloon dilators are traditionally used to dilate esophageal strictures during an...
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Esophageal Manifestations of Dermatological Diseases, Diagnosis, and Management
Purpose of ReviewThe purpose of this article is to discuss the diagnosis and treatment of diseases that affect both the skin and the esophagus.
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Occupational therapy for epidermolysis bullosa: clinical practice guidelines
The purpose of this article is to summarize the Dystrophic Epidermolysis Bullosa Research Association (DEBRA) International evidence-based Clinical...
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Efficacy and tolerability of the investigational topical cream SD-101 (6% allantoin) in patients with epidermolysis bullosa: a phase 3, randomized, double-blind, vehicle-controlled trial (ESSENCE study)
BackgroundEpidermolysis bullosa (EB) is a rare genetic disorder that manifests as blistering and/or skin erosion. There is no approved treatment for...
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Epidermolysis bullosa acquisita
Epidermolysis bullosa acquisita (EBA) is a rare acquired subepidermal bullous autoimmune dermatosis, associated with autoantibodies against collagen...
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Off-Label Uses of Rituximab in Dermatology
Purpose of ReviewRituximab has transformed the treatment of B-cell malignancies and rheumatoid arthritis in the past 2 decades. More recently, this...
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Statistical recommendations for count, binary, and ordinal data in rare disease cross-over trials
BackgroundRecommendations for statistical methods in rare disease trials are scarce, especially for cross-over designs. As a result various...
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Collagen XVII deficiency alters epidermal patterning
Vertebrates exhibit patterned epidermis, exemplified by scales/interscales in mice tails and grooves/ridges on the human skin surface...
