All Stories

  1. A systematic review and meta-analysis of Non-SCORTEN mortality predictors in Stevens Johnson syndrome and toxic epidermal necrolysis
  2. A systematic review and meta-analysis of case-control studies on cytokines in blister fluid and skin of patients with Stevens Johnson syndrome and toxic epidermal necrolysis
  3. Infectious complications of Stevens Johnson syndrome and toxic epidermal necrolysis
  4. Psychological complications of Stevens Johnson syndrome and toxic epidermal necrolysis
  5. Global consensus process to establish a core data set for hidradenitis suppurativa registries
  6. Human dermal fibroblast subpopulations and epithelial mesenchymal transition signals in hidradenitis suppurativa tunnels are normalized by spleen tyrosine kinase antagonism in vivo
  7. The Serum Proteome of Pyoderma Gangrenosum is More Expansive Than That of Hidradenitis Suppurativa
  8. Alterations to the Hidradenitis Suppurativa Serum Proteome with Spleen Tyrosine Kinase Antagonism: Proteomic Results from a Phase 2 Clinical Trial
  9. Clinical reports: the overarching home for case series and case reports in the BJD
  10. Resident cutaneous memory T-cells: A clinical review of their role in chronic inflammatory dermatoses and potential as therapeutic targets
  11. Rapid Attenuation of B-Cell and IFN-γ–Associated Chemokines in Clinical Responders to Jak Inhibition with Upadacitinib in Hidradenitis Suppurativa
  12. Mast cells are upregulated in hidradenitis suppurativa tissue, associated with epithelialized tunnels and normalized by spleen tyrosine kinase antagonism
  13. Maintenance of response to dupilumab in prurigo nodularis: A retrospective cohort study
  14. Obesity and Hidradenitis Suppurativa: Targeting meta-inflammation for therapeutic gain?
  15. Mast cells are upregulated in Hidradenitis Suppurativa Tissue, associated with epithelialized tunnels and normalised by Spleen Tyrosine Kinase Antagonism
  16. Academic dermatology in Australia and New Zealand between 2017 and 2022: A cross‐sectional bibliometric analysis
  17. Baseline clinical, hormonal and molecular markers associated with clinical response to IL ‐23 antagonism in hidradenitis suppurativa: A prospective cohort study
  18. The Impact of Psoriasis Biologic Therapy Upon HIV Viral Load and CD4+ cell counts in HIV Positive Individuals: A Real‐World Cohort Study
  19. Monkeypox: Cutaneous clues to clinical diagnosis
  20. Baseline Clinical, Hormonal and Molecular Markers Associated with Clinical Response to IL-23 Antagonism in Hidradenitis Suppurativa: A Prospective Cohort Study
  21. Human Dermal Fibroblast Subpopulations and Epithelial Mesenchymal Transition Signals in Hidradenitis Suppurativa Tunnels are Normalized by Spleen Tyrosine Kinase Antagonism in Vivo
  22. In Search of Therapeutic Biomarkers to IL-23 Antagonism in Hidradenitis Suppurativa
  23. Treatment of alopecia areata with the janus kinase inhibitor upadacitinib: A retrospective cohort study
  24. Dupilumab-associated head and neck dermatitis resolves temporarily with itraconazole therapy and rapidly with transition to upadacitinib, with Malassezia-specific immunoglobulin E levels mirroring clinical response
  25. Real-world safety and clinical response of Janus kinase inhibitor upadacitinib in the treatment of hidradenitis suppurativa: A retrospective cohort study
  26. Strongyloides screening prior to dupilumab therapy in atopic dermatitis: a retrospective cohort study evaluating screening utility
  27. The road to biologics in patients with hidradenitis suppurativa: a nationwide drug utilization study
  28. Adalimumab therapy is associated with increased faecal short chain fatty acids in hidradenitis suppurativa
  29. ACE2 Expression is Elevated in Tissue of Hidradenitis Suppurativa and Pyoderma Gangrenousm and Demonstrates a Different Pattern of Expression to Psoriasis Vulgaris
  30. Can we increase the drug survival time of biologic therapies in hidradenitis suppurativa?
  31. Interpretation of comorbidity risk in hidradenitis suppurativa: comparing odds ratio and ‘number needed to be exposed’
  32. Interleukin‐17RA blockade by brodalumab decreases inflammatory pathways in hidradenitis suppurativa skin and serum
  33. A case series of early biologic therapy in guttate psoriasis: Targeting resident memory T cell activity as a potential novel therapeutic modality
  34. Extramammary Paget’s disease: Harbinger of internal malignancy
  35. Dupilumab‐associated head and neck dermatitis is associated with elevated pretreatment serum Malassezia ‐specific IgE : a multicentre, prospective cohort study
  36. Amplicon sequencing demonstrates comparable follicular mycobiomes in patients with hidradenitis suppurativa compared with healthy controls
  37. Identification of Biomarkers and Critical Evaluation of Biomarker Validation in Hidradenitis Suppurativa
  38. Pyoderma gangrenosum: A systematic review of the molecular characteristics of disease
  39. The inflammatory proteome of hidradenitis suppurativa skin is more expansive than that of psoriasis vulgaris
  40. The pathogenesis of hidradenitis suppurativa: Evolving paradigms in a complex disease
  41. Guidance on COVID-19 Vaccination in Hidradenitis Suppurativa Patients: A Modified Delphi Consensus of Experts
  42. Biologic therapy is not associated with increased COVID-19 severity in patients with hidradenitis suppurativa: Initial findings from the Global Hidradenitis Suppurativa COVID-19 Registry
  43. High inflammation in hidradenitis suppurativa extends to perilesional skin and can be subdivided by lipocalin-2 expression
  44. Antimicrobial peptides in hidradenitis suppurativa: a systematic review*
  45. Large‐scale serum analysis identifies unique systemic biomarkers in psoriasis and hidradenitis suppurativa*
  46. Autoantibody-Mediated Macrophage Responses Provide the Missing Link between Innate and Adaptive Immune Dysfunction in Hidradenitis Suppurativa
  47. Clinical Considerations in the Management of Hidradenitis Suppurativa in Women:
  48. An Abscess Is Not a Descriptive Term but an Entity With a Universally Accepted Definition—A Clarification on Semantics—Reply
  49. Metabolic syndrome and hidradenitis suppurativa: epidemiological, molecular, and therapeutic aspects
  50. Rapid and sustained remission of synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome with IL-23p19 antagonist (risankizumab)
  51. Assessing the Responsiveness of Sonographic Biomarkers to Brodalumab Therapy in Hidradenitis Suppurativa
  52. Cellular Neurothekeoma
  53. The Impact of Body Mass Index Upon the Efficacy of Adalimumab in Hidradenitis Suppurativa
  54. Therapeutic biomarkers in hidradenitis suppurativa: one step closer to the clinic
  55. Target molecules for future hidradenitis suppurativa treatment
  56. Epithelialized tunnels are a source of inflammation in hidradenitis suppurativa
  57. Ultrasound‐guided de‐roofing of epithelialised tunnels of hidradenitis suppurativa
  58. Global Harmonization of Morphological Definitions in Hidradenitis Suppurativa for a Proposed Glossary
  59. Cover Image
  60. In-Depth Analysis of the Hidradenitis Suppurativa Serum Proteome Identifies Distinct Inflammatory Subtypes
  61. Differential Profiles of Gamma‐Secretase‐Notch Signaling in Hidradenitis Suppurativa: The Need for Genotype‐Endotype‐Phenotype Analysis
  62. Quantifying the natural variation in lesion counts over time in untreated hidradenitis suppurativa: Implications for outcome measures and trial design
  63. The value of case reports in pharmacovigilance
  64. Rapid resolution of pyoderma gangrenosum with brodalumab therapy
  65. The effect of subcutaneous brodalumab on clinical disease activity in hidradenitis suppurativa: An open-label cohort study
  66. The Erythema Q‐score, an Imaging Biomarker for Redness in Skin Inflammation
  67. What causes hidradenitis suppurativa ? – 15 years after
  68. Dermal Tunnels Influence Time to Clinical Response and Family History Influences Time to Loss of Clinical Response in Hidradenitis Suppurativa Patients Treated with Adalimumab
  69. A Systematic Review of Promising Therapeutic Targets in Hidradenitis Suppurativa: A Critical Evaluation of Mechanistic and Clinical Relevance
  70. Weekly Administration of Brodalumab in Hidradenitis Suppurativa: An Open Label Cohort Study
  71. Global Hidradenitis Suppurativa COVID‐19 Registry: a registry to inform data‐driven management practices
  72. Anti–Saccharomyces cervisiae antibodies in hidradenitis suppurativa: More than a gut feeling
  73. Primary imputation methods impact efficacy results in hidradenitis suppurativa clinical trials
  74. A Systematic Review andCritical Appraisal of Metagenomic and Culture Studies in Hidradenitis Suppurativa
  75. Ex Vivo Models and Interpretation of Mechanistic Studies in Hidradenitis Suppurativa
  76. Hidradenitis suppurativa is an autoinflammatory keratinization disease: A review of the clinical, histologic, and molecular evidence
  77. Doppler Ultrasound‐Based Non‐Invasive Biomarkers in Hidradenitis Suppurativa: Evaluation of Analytical and Clinical Validity
  78. The Importance of Methodological Rigor in Proof-of-Concept Clinical Trials: A Lesson from Hidradenitis Suppurativa
  79. Malignancy and infection risk during adalimumab therapy in hidradenitis suppurativa
  80. The Asia Pacific Hidradenitis Suppurativa (APHiS) foundation: promoting hidradenitis suppurativa research in the Asia Pacific
  81. COVID-19 and immunomodulator/immunosuppressant use in dermatology
  82. Clinical response rates, placebo response rates, and significantly associated covariates are dependent on choice of outcome measure in hidradenitis suppurativa: A post hoc analysis of PIONEER 1 and 2 individual patient data
  83. Beyond antibodies: B cells in Hidradenitis Suppurativa: Bystanders, contributors or therapeutic targets?
  84. Interleukin 17C is elevated in lesional tissue of hidradenitis suppurativa
  85. Integrating complement into the molecular pathogenesis of Hidradenitis Suppurativa
  86. No evidence that impaired Notch signalling differentiates hidradenitis suppurativa from other inflammatory skin diseases
  87. A Scoping Review of Non-invasive Imaging Modalities in Dermatological Disease: Potential Novel Biomarkers in Hidradenitis Suppurativa
  88. Prevalence of inflammatory bowel disease (IBD) in hidradenitis suppurativa (HS): systematic review and adjusted meta‐analysis
  89. Consensus definitions of disease activity in hidradenitis suppurativa: crossing the semantic gap
  90. Epidermolizis bülloza yaşam kalitesi puanlarının klinik uygulamalarının geliştirilmesi: QOLEB anketinde klinik olarak anlamlı sonuçların tanımlanması
  91. In silico Analysis of Gamma-Secretase-Complex Mutations in Hidradenitis Suppurativa Demonstrates Disease-Specific Substrate Recognition and Cleavage Alterations
  92. Putting nodule counts behind us: hidradenitis suppurativa outcome measures independent of descriptive semantics
  93. Defining lesional, perilesional and unaffected skin in hidradenitis suppurativa: proposed recommendations for clinical trials and translational research studies
  94. Specimen Collection for Translational Studies in Hidradenitis Suppurativa
  95. Into the (gluteal) fold: pilonidal disease and hidradenitis suppurativa – association or continuum?
  96. Contribution of fibroblasts to tunnel formation and inflammation in hidradenitis suppurativa/ acne inversa
  97. A systematic review and critical evaluation of immunohistochemical associations in hidradenitis suppurativa
  98. A systematic review of reported cases of pachyonychia congenita tarda
  99. Lack of photographic documentation undermines assessment of hidradenitis suppurativa phenotypes: reply from the author
  100. Inter‐rater reliability of phenotypes and exploratory genotype–phenotype analysis in inherited hidradenitis suppurativa
  101. The contradictory inefficacy of methotrexate in hidradenitis suppurativa: a need to revise pathogenesis or acknowledge disease heterogeneity?
  102. Assessing the efficacy of new biologic therapies in hidradenitis suppurativa: consistency vs. bias in outcome measures in moderate and severe disease
  103. Hidradenitis suppurativa and diabetes: big data bias masks a true association
  104. The Hygiene Hypothesis, Old Friends, and New Genes
  105. Commentary: Hidradenitis Suppurativa: A Systematic Review Integrating Inflammatory Pathways Into a Cohesive Pathogenic Model
  106. Cutaneous neonatal Langerhans cell histiocytosis: a systematic review of case reports
  107. Topical, systemic and biologic therapies in hidradenitis suppurativa: pathogenic insights by examining therapeutic mechanisms
  108. Proceeding report of the Second Symposium on Hidradenitis Suppurativa Advances (SHSA) 2017
  109. A systematic review and critical evaluation of inflammatory cytokine associations in hidradenitis suppurativa
  110. A systematic review and critical evaluation of immunohistochemical associations in hidradenitis suppurativa
  111. Complement, Hidradenitis Suppurativa and Pathogen-Driven Positive Selection
  112. We Need to Talk About Notch:Notch Dysregulation as an Epiphenomenon in Inflammatory Skin Disease
  113. A Retrospective Cohort Study of Melanoma Prevalence Stratified by Body Site in a Regional Australian Population 1994-2017: Site-Specific Protective Mechanisms
  114. New therapeutics for itch in dermatomyositis
  115. Secukinumab in pityriasis rubra pilaris: A case series demonstrating variable response and the need for minimal clinical datasets
  116. Quality-of-Life Measures in Hidradenitis Suppurativa: The Importance of High-Quality Methodology and Standards
  117. BJD research letters: concise, thought provoking and of general interest
  118. Hidradenitis suppurativa, a review of pathogenesis, associations and management. Part 1
  119. Drug-associated hidradenitis suppurativa: A systematic review of case reports
  120. Pharmaceutical Benefits Scheme listing of adalimumab for hidradenitis suppurativa: Is hidradenitis suppurativa a life-changing drug or does lifestyle change the drug?
  121. HLA-B*1502 haplotype screening prior to carbamazepine administration in individuals of south-east Asian ancestry nears cost-effectiveness in preventing severe cutaneous adverse drug reactions
  122. Disease-specific health related quality of life patient reported outcome measures in Genodermatoses: a systematic review and critical evaluation
  123. A systematic review and critical evaluation of reported pathogenic sequence variants in hidradenitis suppurativa
  124. Lichen amyloidosis involving the scalp
  125. Psoriasis in those planning a family, pregnant or breast-feeding. The Australasian Psoriasis Collaboration
  126. Highly Resistant Acrodermatitis Continua of Hallopeau and Pustular Psoriasis
  127. Beyond the tip of the iceberg: the role of phosphoinositide 3-kinase/AKT in acne inversa/hidradenitis suppurativa
  128. The early bird and the worm: a case of cercarial dermatitis
  129. Adopting the orphan: The importance of recognising hidradenitis suppurativa as a systemic auto-inflammatory disease
  130. Tattoo-associated mycobacterial infections: an emerging public health issue
  131. Fifty shades of yellow: a review of the xanthodermatoses
  132. Adalimumab-induced porokeratosis
  133. Chlorophyll‐induced pseudoporphyria with ongoing photosensitivity after cessation – a case series of four patients
  134. Phenotypic heterogeneity implies heterogeneous pathogenic pathways in hidradenitis suppurativa
  135. Multinucleate Cell Angiohistiocytoma
  136. Autoimmune Blistering Diseases and Corticosteroid Use: A Review of the Evidence
  137. Cyclophosphamide in Autoimmune Blistering Diseases: Safety, Efficacy and Evidence Base
  138. Living with Epidermolysis Bullosa: Reviewing the Impact on Individuals’ Quality of Life
  139. The clinical significance of drug interactions between dermatological and psychoactive medications
  140. Health-related Quality of Life in Epidermolysis Bullosa: Validation of the Dutch QOLEB Questionnaire and Assessment in the Dutch Population
  141. A phase II randomized vehicle-controlled trial of intradermal allogeneic fibroblasts for recessive dystrophic epidermolysis bullosa
  142. The development and validation of the Treatment of Autoimmune Bullous Disease Quality of Life questionnaire, a tool to measure the quality of life impacts of treatments used in patients with autoimmune blistering disease
  143. Measuring quality of life in epidermolysis bullosa in Mexico: Cross-cultural validation of the Hispanic version of the Quality of Life in Epidermolysis Bullosa questionnaire
  144. Development of a Quality-of-Life Instrument for Autoimmune Bullous Disease
  145. Diffuse melanosis cutis: A systematic review of the literature
  146. Corticosteroid Use in Autoimmune Blistering Diseases
  147. Quality-of-Life Measurement in Blistering Diseases
  148. Corticosteroid Use in Autoimmune Blistering Diseases
  149. Evidence-Based Treatments in Pemphigus Vulgaris and Pemphigus Foliaceus
  150. Current Management Strategies in Paraneoplastic Pemphigus (Paraneoplastic Autoimmune Multiorgan Syndrome)
  151. Paraneoplastic Pemphigus (Paraneoplastic Autoimmune Multiorgan Syndrome): Clinical Presentations and Pathogenesis
  152. No Evidence That Human Papillomavirus Is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma
  153. Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagen
  154. Categorizing immunofluorescence mapping in epidermolysis bullosa with pyloric atresia: Use as a broad prognostic indicator
  155. Erratum
  156. Quality of Life Measurements in Epidermolysis Bullosa: Tools for Clinical Research and Patient Care
  157. Quality of life evaluation in epidermolysis bullosa (EB) through the development of the QOLEB questionnaire: an EB-specific quality of life instrument
  158. Performing surgery with a single electron: electrosurgery and quantum mechanics
  159. A ski and adventure camp for young patients with severe forms of epidermolysis bullosa