All Stories

  1. Pyoderma Gangrenosum: A Retrospective Cohort Study of Comorbidities and Therapies in Over 65,000 Patients in the TriNetX Database
  2. Efficacy of Biologics for Hidradenitis Suppurativa: A Network Meta Analysis and Meta Regression for Baseline Disease Severity
  3. Predictors of Survival and Length of Stay in Steven Johnson syndrome and toxic epidermal necrolysis: A single centre retrospective study of 111 patients
  4. Real‐World Efficacy and Drug Survival of Adalimumab in Australian Patients With Psoriasis
  5. Psychological Complications of Stevens‐Johnson Syndrome and Toxic Epidermal Necrolysis: A Systematic Review and Meta‐Analysis
  6. Time to Recognise Psoriasis as a Cardiovascular Risk Modifier in National Guidance
  7. Prevalence and predictors of posttraumatic stress disorder in Stevens Johnson syndrome and toxic epidermal necrolysis
  8. The effects of isotretinoin on serum thyroid parameters: A systematic review and meta-analysis
  9. Sequencing of Biologic Therapy in Hidradenitis Suppurativa: A Real‐World Analysis of Treatment in Over 15,000 Patients
  10. Unravelling the complex pathogenesis of hidradenitis suppurativa
  11. Malignancy Risk Differs Between Hidradenitis Suppurativa and Pilonidal Sinus Disease:
  12. Quantifying time to medical and/or surgical therapy after diagnosis of hidradenitis suppurativa and pilonidal sinus disease: A propensity‐matched real‐world cohort analysis
  13. Intrinsic factors in the pathogenesis of hidradenitis suppurativa: Genetics, hormones, and the microbiome
  14. Australasian hidradenitis suppurativa management guidelines
  15. The Clinical and Molecular Response of Pyoderma Gangrenosum to IL-23 Blockade: Result from a Proof-of-Concept Open-Label Clinical Trial
  16. Systematic review and meta‐analysis of non‐SCORTEN predictors of mortality in Stevens‐Johnson syndrome and toxic epidermal necrolysis
  17. Infectious complications of Stevens‐Johnson syndrome and toxic epidermal necrolysis: A systematic review and meta‐analysis
  18. A systematic review of case–control studies of cytokines in blister fluid and skin tissue of patients with Stevens Johnson syndrome and toxic epidermal necrolysis
  19. Tissue comparability and bias in hidradenitis suppurativa transcriptomic studies
  20. A systematic review and meta-analysis of Non-SCORTEN mortality predictors in Stevens Johnson syndrome and toxic epidermal necrolysis
  21. 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
  22. Infectious complications of Stevens Johnson syndrome and toxic epidermal necrolysis
  23. Psychological complications of Stevens Johnson syndrome and toxic epidermal necrolysis
  24. Global consensus process to establish a core data set for hidradenitis suppurativa registries
  25. Human dermal fibroblast subpopulations and epithelial mesenchymal transition signals in hidradenitis suppurativa tunnels are normalized by spleen tyrosine kinase antagonism in vivo
  26. The Serum Proteome of Pyoderma Gangrenosum is More Expansive Than That of Hidradenitis Suppurativa
  27. Alterations to the Hidradenitis Suppurativa Serum Proteome with Spleen Tyrosine Kinase Antagonism: Proteomic Results from a Phase 2 Clinical Trial
  28. Clinical reports: the overarching home for case series and case reports in the BJD
  29. Resident cutaneous memory T-cells: A clinical review of their role in chronic inflammatory dermatoses and potential as therapeutic targets
  30. Rapid Attenuation of B-Cell and IFN-γ–Associated Chemokines in Clinical Responders to Jak Inhibition with Upadacitinib in Hidradenitis Suppurativa
  31. Mast cells are upregulated in hidradenitis suppurativa tissue, associated with epithelialized tunnels and normalized by spleen tyrosine kinase antagonism
  32. Maintenance of response to dupilumab in prurigo nodularis: A retrospective cohort study
  33. Obesity and Hidradenitis Suppurativa: Targeting meta-inflammation for therapeutic gain?
  34. Mast cells are upregulated in Hidradenitis Suppurativa Tissue, associated with epithelialized tunnels and normalised by Spleen Tyrosine Kinase Antagonism
  35. Academic dermatology in Australia and New Zealand between 2017 and 2022: A cross‐sectional bibliometric analysis
  36. Baseline clinical, hormonal and molecular markers associated with clinical response to IL ‐23 antagonism in hidradenitis suppurativa: A prospective cohort study
  37. The Impact of Psoriasis Biologic Therapy Upon HIV Viral Load and CD4+ cell counts in HIV Positive Individuals: A Real‐World Cohort Study
  38. Monkeypox: Cutaneous clues to clinical diagnosis
  39. Baseline Clinical, Hormonal and Molecular Markers Associated with Clinical Response to IL-23 Antagonism in Hidradenitis Suppurativa: A Prospective Cohort Study
  40. Human Dermal Fibroblast Subpopulations and Epithelial Mesenchymal Transition Signals in Hidradenitis Suppurativa Tunnels are Normalized by Spleen Tyrosine Kinase Antagonism in Vivo
  41. In Search of Therapeutic Biomarkers to IL-23 Antagonism in Hidradenitis Suppurativa
  42. Treatment of alopecia areata with the janus kinase inhibitor upadacitinib: A retrospective cohort study
  43. 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
  44. Real-world safety and clinical response of Janus kinase inhibitor upadacitinib in the treatment of hidradenitis suppurativa: A retrospective cohort study
  45. Strongyloides screening prior to dupilumab therapy in atopic dermatitis: a retrospective cohort study evaluating screening utility
  46. The road to biologics in patients with hidradenitis suppurativa: a nationwide drug utilization study
  47. Adalimumab therapy is associated with increased faecal short chain fatty acids in hidradenitis suppurativa
  48. ACE2 Expression is Elevated in Tissue of Hidradenitis Suppurativa and Pyoderma Gangrenousm and Demonstrates a Different Pattern of Expression to Psoriasis Vulgaris
  49. Can we increase the drug survival time of biologic therapies in hidradenitis suppurativa?
  50. Interpretation of comorbidity risk in hidradenitis suppurativa: comparing odds ratio and ‘number needed to be exposed’
  51. Interleukin‐17RA blockade by brodalumab decreases inflammatory pathways in hidradenitis suppurativa skin and serum
  52. A case series of early biologic therapy in guttate psoriasis: Targeting resident memory T cell activity as a potential novel therapeutic modality
  53. Extramammary Paget’s disease: Harbinger of internal malignancy
  54. Dupilumab‐associated head and neck dermatitis is associated with elevated pretreatment serum Malassezia ‐specific IgE : a multicentre, prospective cohort study
  55. Amplicon sequencing demonstrates comparable follicular mycobiomes in patients with hidradenitis suppurativa compared with healthy controls
  56. Identification of Biomarkers and Critical Evaluation of Biomarker Validation in Hidradenitis Suppurativa
  57. Pyoderma gangrenosum: A systematic review of the molecular characteristics of disease
  58. The inflammatory proteome of hidradenitis suppurativa skin is more expansive than that of psoriasis vulgaris
  59. The pathogenesis of hidradenitis suppurativa: Evolving paradigms in a complex disease
  60. Guidance on COVID-19 Vaccination in Hidradenitis Suppurativa Patients: A Modified Delphi Consensus of Experts
  61. 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
  62. High inflammation in hidradenitis suppurativa extends to perilesional skin and can be subdivided by lipocalin-2 expression
  63. Antimicrobial peptides in hidradenitis suppurativa: a systematic review*
  64. Large‐scale serum analysis identifies unique systemic biomarkers in psoriasis and hidradenitis suppurativa*
  65. Autoantibody-Mediated Macrophage Responses Provide the Missing Link between Innate and Adaptive Immune Dysfunction in Hidradenitis Suppurativa
  66. Clinical Considerations in the Management of Hidradenitis Suppurativa in Women:
  67. An Abscess Is Not a Descriptive Term but an Entity With a Universally Accepted Definition—A Clarification on Semantics—Reply
  68. Metabolic syndrome and hidradenitis suppurativa: epidemiological, molecular, and therapeutic aspects
  69. Rapid and sustained remission of synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome with IL-23p19 antagonist (risankizumab)
  70. Assessing the Responsiveness of Sonographic Biomarkers to Brodalumab Therapy in Hidradenitis Suppurativa
  71. Cellular Neurothekeoma
  72. The Impact of Body Mass Index Upon the Efficacy of Adalimumab in Hidradenitis Suppurativa
  73. Therapeutic biomarkers in hidradenitis suppurativa: one step closer to the clinic
  74. Target molecules for future hidradenitis suppurativa treatment
  75. Epithelialized tunnels are a source of inflammation in hidradenitis suppurativa
  76. Ultrasound‐guided de‐roofing of epithelialised tunnels of hidradenitis suppurativa
  77. Global Harmonization of Morphological Definitions in Hidradenitis Suppurativa for a Proposed Glossary
  78. Cover Image
  79. In-Depth Analysis of the Hidradenitis Suppurativa Serum Proteome Identifies Distinct Inflammatory Subtypes
  80. Differential Profiles of Gamma‐Secretase‐Notch Signaling in Hidradenitis Suppurativa: The Need for Genotype‐Endotype‐Phenotype Analysis
  81. Quantifying the natural variation in lesion counts over time in untreated hidradenitis suppurativa: Implications for outcome measures and trial design
  82. The value of case reports in pharmacovigilance
  83. Rapid resolution of pyoderma gangrenosum with brodalumab therapy
  84. The effect of subcutaneous brodalumab on clinical disease activity in hidradenitis suppurativa: An open-label cohort study
  85. The Erythema Q‐score, an Imaging Biomarker for Redness in Skin Inflammation
  86. What causes hidradenitis suppurativa ? – 15 years after
  87. Dermal Tunnels Influence Time to Clinical Response and Family History Influences Time to Loss of Clinical Response in Hidradenitis Suppurativa Patients Treated with Adalimumab
  88. A Systematic Review of Promising Therapeutic Targets in Hidradenitis Suppurativa: A Critical Evaluation of Mechanistic and Clinical Relevance
  89. Weekly Administration of Brodalumab in Hidradenitis Suppurativa: An Open Label Cohort Study
  90. Global Hidradenitis Suppurativa COVID‐19 Registry: a registry to inform data‐driven management practices
  91. Anti–Saccharomyces cervisiae antibodies in hidradenitis suppurativa: More than a gut feeling
  92. Primary imputation methods impact efficacy results in hidradenitis suppurativa clinical trials
  93. A Systematic Review andCritical Appraisal of Metagenomic and Culture Studies in Hidradenitis Suppurativa
  94. Ex Vivo Models and Interpretation of Mechanistic Studies in Hidradenitis Suppurativa
  95. Hidradenitis suppurativa is an autoinflammatory keratinization disease: A review of the clinical, histologic, and molecular evidence
  96. Doppler Ultrasound‐Based Non‐Invasive Biomarkers in Hidradenitis Suppurativa: Evaluation of Analytical and Clinical Validity
  97. The Importance of Methodological Rigor in Proof-of-Concept Clinical Trials: A Lesson from Hidradenitis Suppurativa
  98. Malignancy and infection risk during adalimumab therapy in hidradenitis suppurativa
  99. The Asia Pacific Hidradenitis Suppurativa (APHiS) foundation: promoting hidradenitis suppurativa research in the Asia Pacific
  100. COVID-19 and immunomodulator/immunosuppressant use in dermatology
  101. 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
  102. Beyond antibodies: B cells in Hidradenitis Suppurativa: Bystanders, contributors or therapeutic targets?
  103. Interleukin 17C is elevated in lesional tissue of hidradenitis suppurativa
  104. Integrating complement into the molecular pathogenesis of Hidradenitis Suppurativa
  105. No evidence that impaired Notch signalling differentiates hidradenitis suppurativa from other inflammatory skin diseases
  106. A Scoping Review of Non-invasive Imaging Modalities in Dermatological Disease: Potential Novel Biomarkers in Hidradenitis Suppurativa
  107. Prevalence of inflammatory bowel disease (IBD) in hidradenitis suppurativa (HS): systematic review and adjusted meta‐analysis
  108. Consensus definitions of disease activity in hidradenitis suppurativa: crossing the semantic gap
  109. Epidermolizis bülloza yaşam kalitesi puanlarının klinik uygulamalarının geliştirilmesi: QOLEB anketinde klinik olarak anlamlı sonuçların tanımlanması
  110. In silico Analysis of Gamma-Secretase-Complex Mutations in Hidradenitis Suppurativa Demonstrates Disease-Specific Substrate Recognition and Cleavage Alterations
  111. Putting nodule counts behind us: hidradenitis suppurativa outcome measures independent of descriptive semantics
  112. Defining lesional, perilesional and unaffected skin in hidradenitis suppurativa: proposed recommendations for clinical trials and translational research studies
  113. Specimen Collection for Translational Studies in Hidradenitis Suppurativa
  114. Into the (gluteal) fold: pilonidal disease and hidradenitis suppurativa – association or continuum?
  115. Contribution of fibroblasts to tunnel formation and inflammation in hidradenitis suppurativa/ acne inversa
  116. A systematic review and critical evaluation of immunohistochemical associations in hidradenitis suppurativa
  117. A systematic review of reported cases of pachyonychia congenita tarda
  118. Lack of photographic documentation undermines assessment of hidradenitis suppurativa phenotypes: reply from the author
  119. Inter‐rater reliability of phenotypes and exploratory genotype–phenotype analysis in inherited hidradenitis suppurativa
  120. The contradictory inefficacy of methotrexate in hidradenitis suppurativa: a need to revise pathogenesis or acknowledge disease heterogeneity?
  121. Assessing the efficacy of new biologic therapies in hidradenitis suppurativa: consistency vs. bias in outcome measures in moderate and severe disease
  122. Hidradenitis suppurativa and diabetes: big data bias masks a true association
  123. The Hygiene Hypothesis, Old Friends, and New Genes
  124. Commentary: Hidradenitis Suppurativa: A Systematic Review Integrating Inflammatory Pathways Into a Cohesive Pathogenic Model
  125. Cutaneous neonatal Langerhans cell histiocytosis: a systematic review of case reports
  126. Topical, systemic and biologic therapies in hidradenitis suppurativa: pathogenic insights by examining therapeutic mechanisms
  127. Proceeding report of the Second Symposium on Hidradenitis Suppurativa Advances (SHSA) 2017
  128. A systematic review and critical evaluation of inflammatory cytokine associations in hidradenitis suppurativa
  129. A systematic review and critical evaluation of immunohistochemical associations in hidradenitis suppurativa
  130. Complement, Hidradenitis Suppurativa and Pathogen-Driven Positive Selection
  131. We Need to Talk About Notch:Notch Dysregulation as an Epiphenomenon in Inflammatory Skin Disease
  132. A Retrospective Cohort Study of Melanoma Prevalence Stratified by Body Site in a Regional Australian Population 1994-2017: Site-Specific Protective Mechanisms
  133. New therapeutics for itch in dermatomyositis
  134. Secukinumab in pityriasis rubra pilaris: A case series demonstrating variable response and the need for minimal clinical datasets
  135. Quality-of-Life Measures in Hidradenitis Suppurativa: The Importance of High-Quality Methodology and Standards
  136. BJD research letters: concise, thought provoking and of general interest
  137. Hidradenitis suppurativa, a review of pathogenesis, associations and management. Part 1
  138. Drug-associated hidradenitis suppurativa: A systematic review of case reports
  139. Pharmaceutical Benefits Scheme listing of adalimumab for hidradenitis suppurativa: Is hidradenitis suppurativa a life-changing drug or does lifestyle change the drug?
  140. 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
  141. Disease-specific health related quality of life patient reported outcome measures in Genodermatoses: a systematic review and critical evaluation
  142. A systematic review and critical evaluation of reported pathogenic sequence variants in hidradenitis suppurativa
  143. Lichen amyloidosis involving the scalp
  144. Psoriasis in those planning a family, pregnant or breast-feeding. The Australasian Psoriasis Collaboration
  145. Highly Resistant Acrodermatitis Continua of Hallopeau and Pustular Psoriasis
  146. Beyond the tip of the iceberg: the role of phosphoinositide 3-kinase/AKT in acne inversa/hidradenitis suppurativa
  147. The early bird and the worm: a case of cercarial dermatitis
  148. Adopting the orphan: The importance of recognising hidradenitis suppurativa as a systemic auto-inflammatory disease
  149. Tattoo-associated mycobacterial infections: an emerging public health issue
  150. Fifty shades of yellow: a review of the xanthodermatoses
  151. Adalimumab-induced porokeratosis
  152. Chlorophyll‐induced pseudoporphyria with ongoing photosensitivity after cessation – a case series of four patients
  153. Phenotypic heterogeneity implies heterogeneous pathogenic pathways in hidradenitis suppurativa
  154. Multinucleate Cell Angiohistiocytoma
  155. Autoimmune Blistering Diseases and Corticosteroid Use: A Review of the Evidence
  156. Cyclophosphamide in Autoimmune Blistering Diseases: Safety, Efficacy and Evidence Base
  157. Living with Epidermolysis Bullosa: Reviewing the Impact on Individuals’ Quality of Life
  158. The clinical significance of drug interactions between dermatological and psychoactive medications
  159. Health-related Quality of Life in Epidermolysis Bullosa: Validation of the Dutch QOLEB Questionnaire and Assessment in the Dutch Population
  160. A phase II randomized vehicle-controlled trial of intradermal allogeneic fibroblasts for recessive dystrophic epidermolysis bullosa
  161. 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
  162. 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
  163. Development of a Quality-of-Life Instrument for Autoimmune Bullous Disease
  164. Diffuse melanosis cutis: A systematic review of the literature
  165. Corticosteroid Use in Autoimmune Blistering Diseases
  166. Quality-of-Life Measurement in Blistering Diseases
  167. Corticosteroid Use in Autoimmune Blistering Diseases
  168. Evidence-Based Treatments in Pemphigus Vulgaris and Pemphigus Foliaceus
  169. Current Management Strategies in Paraneoplastic Pemphigus (Paraneoplastic Autoimmune Multiorgan Syndrome)
  170. Paraneoplastic Pemphigus (Paraneoplastic Autoimmune Multiorgan Syndrome): Clinical Presentations and Pathogenesis
  171. No Evidence That Human Papillomavirus Is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma
  172. Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagen
  173. Categorizing immunofluorescence mapping in epidermolysis bullosa with pyloric atresia: Use as a broad prognostic indicator
  174. Erratum
  175. Quality of Life Measurements in Epidermolysis Bullosa: Tools for Clinical Research and Patient Care
  176. Quality of life evaluation in epidermolysis bullosa (EB) through the development of the QOLEB questionnaire: an EB-specific quality of life instrument
  177. Performing surgery with a single electron: electrosurgery and quantum mechanics
  178. A ski and adventure camp for young patients with severe forms of epidermolysis bullosa