• <em>Staphylococcus aureus</em> proteases trigger eosinophil-mediated skin inflammation
• A CASE OF ALLERGIC RHINITIS WHO HAS DEVELOPED EOSINOPHILIC PNEUMONIA, FOLLOWED BY EOSINOPHILIC CELLULITIS
• A case of cryopyrin-associated periodic syndrome due to somatic mosaic mutation complicated with recurrent circinate erythematous psoriasis
• A Case of Well Leg Compartment Syndrome After Robot-assisted Laparoscopic Prostatectomy:With Review
• A novel Nlrp3 knock-in mouse model with hyperactive inflammasome in development of lethal inflammation
• A population-scale temporal case-control evaluation of COVID-19 disease phenotype and related outcome rates in patients with cancer in England (UKCCP)
• A Quadruplex Ultrasensitive Immunoassay for Simultaneous Assessment of Human Reproductive Hormone Proteins in Multiple Biofluid Samples
• A spectrum of TP63-related disorders with eight affected individuals in five unrelated families
• A three-generation Muckle-Wells syndrome family: Detailed family history, physical examination, and inter-departmental collaboration
• A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy
• AA amyloidosis complicating cryopyrin-associated periodic syndrome: a study of 86 cases including 23 French patients and systematic review
• Adult patient diagnosed with Muckle-Wells syndrome, antiphospholipid syndrome and glomerular haematuria
• AMPK activation improves recovery from pneumonia-induced lung injury via reduction of er-stress and apoptosis in alveolar epithelial cells
• An orange peel-like nodule on the back: A case of Wells syndrome
• Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
• Annular pustular crusted plaques as unusual cutaneous presentation of systemic lupus erythematosus
• Atypical Wells syndrome successfully treated with dupilumab
• Azathioprine combined with corticosteroids for recurrent cutaneous necrotizing eosinophilic vasculitis secondary to eosinophilic dermatitis
• Bilateral buttock eosinophilic cellulitis after intramuscular benzathine penicillin injection
• Bilateral Optic Disc Swelling as a Plausible Common Ocular Sign of Autoinflammatory Diseases: Report of Three Patients with Blau Syndrome or Cryopyrin-Associated Periodic Syndrome
• Bullous Wells Syndrome Induced by Ustekinumab
• Case report: The altered rate of monocytic cell death in a patient of Muckle-Wells syndrome with atypical clinical course
• Clinical Characteristics of Cryopyrin-Associated Periodic Syndrome and Long-Term Real-World Efficacy and Tolerability of Canakinumab in Japan: Results of a Nationwide Survey
• Clinical Entity Mimicking Infectious Cellulitis: Eosinophilic Cellulitis (Wells' Syndrome)
• Clinical outcomes and safety of anakinra in the treatment of multisystem inflammatory syndrome in children: a single center observational study
• Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulation
• Diagnostic difficulties in pediatric annular dermatoses
• Dimethyl fumarate induced Wells syndrome. A case report
• Discovery and characterization of a specific inhibitor of serine-threonine kinase cyclin-dependent kinase-like 5 (CDKL5) demonstrates role in hippocampal CA1 physiology
• Dupilumab in eosinophilic cellulitis (Wells' syndrome) - case report of a potential new treatment option
• Edematous Plaque on the Elbow of an Infant
• Effectiveness of a comprehensive tele-empowerment programme on self-care behaviours, uncertainty and readmission of patients with heart failure: protocol for a randomised controlled trial
• Effects of TP63 mutations on keratinocyte adhesion and migration
• Efficacy of canakinumab on AA amyloidosis in late-onset NLRP3-associated autoinflammatory disease with an I574F somatic mosaic mutation
• Eosinophilic Annular Erythema: A New Entity of Eosinophilic Dermatosis
• Eosinophilic cellulitis (Wells' syndrome) in a female pediatric patient
• Eosinophilic cellulitis in response to BNT162b2 COVID-19 vaccination
• Eosinophilic Dermatitis due to Triptorelin Pamoate in a Patient with Prostate Cancer Confirmed by Patch Testing
• Eosinophilic Dermatosis of Hematologic Malignancy: Emerging Evidence for the Role of Insect Bites-A Retrospective Clinico-Pathological Study of 35 Cases
• Equally potent: Nlrp3 mutation in macrophages or neutrophils is sufficient to drive autoinflammation
• Equine bronchial epithelial cells are susceptible to cell entry with a SARS-CoV-2 pseudovirus but reveal low replication efficiency
• Evaluation of the inpatient use of inotuzumab ozogamicin and creation of appropriate use guidelines
• Fever, abdominal pain, serositis, arthralgia, hearing loss, proteinuria, and a family history: Muckle Wells syndrome
• Flame figures-eosinophils setting the skin on fire
• Glucose-oxygen deprivation constrains HMGCR function and Rac1 prenylation and activates the NLRP3 inflammasome in human monocytes
• Hay-Wells Syndrome: the challenges of a nine-year follow-up
• Hyperactivation of the JAK2/STAT5 Signaling Pathway and Evaluation of Baricitinib Treatment Among Patients With Eosinophilic Cellulitis
• Identification of a variant in NLRP3 gene in a patient with Muckle-Wells syndrome: a case report and review of literature
• Idiopathic hypereosinophilic syndrome with eosinophilic cellulitis-like cutaneous involvement treated with mepolizumab and dapsone
• In-vitro NLRP3 functional test assists the diagnosis of cryopyrin-associated periodic syndrome (CAPS) patients: A Brazilian cooperation
• Individual life histories: neither slow nor fast, just diverse
• Inflammasome activity is controlled by ZBTB16-dependent SUMOylation of ASC
• Intraoperative pressure monitoring of the lower leg for preventing compression-related complications associated with the lithotomy position
• JT002, a small molecule inhibitor of the NLRP3 inflammasome for the treatment of autoinflammatory disorders
• Lower leg blood pressure decreases while calf external pressure increases with the angulation of the Trendelenburg position in the lithotomy position with calf- and foot-supported leg holders
• LY6E is a pan-coronavirus restriction factor in the respiratory tract
• Megakaryocyte NLRP3 hyperactivation induces mild anemia and potentiates inflammatory response in mice
• Mepolizumab is highly effective in a rare case of Wells syndrome: Eosinophilic granulomatosis with polyangiitis overlap
• Molecular Modeling Analysis Provides Genotype-Phenotype Correlation Insights in a Patient with Ankyloblepharon-Ectodermal Dysplasia-Clefting Syndrome
• Multiple molecular diagnoses in the field of intellectual disability and congenital anomalies: 3.5% of all positive cases
• Myocardial hypertrophy in a patient with eosinophilic dermatitis
• Neutrophilic and eosinophilic dermatoses associated with hematological malignancy
• Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-up
• Ocular involvement in adult and paediatric patients with monogenic autoinflammatory diseases: a Spanish multicentre retrospective study
• Overlap between EEC and AEC syndrome and immunodeficiency in a preterm infant with a TP63 variant
• Pharmacology of a Potent and Novel Inhibitor of the NOD-Like Receptor Pyrin Domain-Containing Protein 3 (NLRP3) Inflammasome that Attenuates Development of Nonalcoholic Steatohepatitis and Liver Fibrosis
• Preventing well leg compartment syndrome among patients in the lithotomy position-Operating room nurses' perspectives: A qualitative study
• Protracted febrile myalgia as a first and challenging manifestation of familial Mediterranean fever
• PU.1 is required to restrain myelopoiesis during chronic inflammatory stress
• Rare Clinical Case of Cryopyrin-associated Periodic Syndrome Presented with Ankylosing Spondylitis: A Case Report
• Rare presentation of Wells syndrome mimicking angioedema: a case report
• Reactogenicity and immunogenicity of the second COVID-19 vaccination in patients with inborn errors of immunity or mannan-binding lectin deficiency
• Real-world safety and effectiveness of canakinumab in patients with cryopyrin-associated periodic fever syndrome: a long-term observational study in Japan
• Recent Advances in Methods for Analyzing Lipids and Fatty Acids
• Relationships between self-perceived and clinical expression of pain and function differ based on the underlying pathology of the human hip
• Revolutionizing Dupilumab Treatment in Refractory Eosinophilic Cellulitis: A Case Report and Comprehensive Literature Review
• RUNX1 mutations mitigate quiescence to promote transformation of hematopoietic progenitors in Fanconi anemia
• Socio-professional impact and quality of life of cryopyrin-associated periodic syndromes in 54 patients in adulthood
• Spectrum of auto-inflammatory diseases in Morocco: a monocentric experience
• Successful Treatment of Minocycline-Induced Facial Hyperpigmentation with a Combination of Chemical Peels and Intense Pulsed Light
• Sweet and Wells syndrome: One disease with different cellular infiltrates?
• Systemic autoinflammatory diseases in pediatric population
• The mismatch negativity as an index of cognitive abilities in adults with Down syndrome
• Toxocariasis and Strongyloidiasis as Triggering Factors for Wells' Syndrome
• TP63-related disorders: two case reports and a brief review of the literature
• Treatment of Eosinophilic Annular Erythema: Retrospective multicenter study and literature review
• Unusual manifestations of adrenal insufficiency: A case report of hypopituitarism and Well's syndrome after apoplexy of a silent pituitary gonadotropic adenoma
• Urticarial vasculitis: Clinical and laboratory findings with a particular emphasis on differential diagnosis
• Wells Syndrome
• Wells syndrome and acquired cutis laxa: An atypical association
• Wells syndrome as a presenting sign of COVID-19 in the setting of allergic rhinitis and iron deficiency anemia
• Wells syndrome confined to the back of the hands mimicking contact dermatitis
• Wells syndrome following vaccination: A pediatric case with positive patch test to gelatin
• Wells Syndrome Presenting as Atypical Periorbital Cellulitis
• Wells syndrome successfully treated with dupilumab
• Wells Syndrome with Generalized Oedema
• Wells Syndrome-Like Histologic Pattern Caused by a Permanent Tattoo
• Wells' Syndrome associated with COVID-19 vaccination
• Wells' syndrome following Oxford-AstraZeneca COVID-19 vaccination
• Wells' syndrome possibly caused by hematologic malignancy, influenza vaccination or ibrutinib: A case report