Search
for
Sort by
Research 31–60 of 47
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside
- Hair follicle immune privilege and its collapse in alopecia areata
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Alopecia areata
- How Our Microbiome Influences the Pathogenesis of Alopecia Areata
- Serum-Based Assessment of Alopecia Areata Response to Treatment Using ATR-FTIR Spectroscopy
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Alopecia areata
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- Multiomic Characterization of Treatment Response to JAK Inhibition in Patients with APECED
- APECED: JAK Inhibition in an Adult Case with Long-Term Follow-up
- Overcoming genetic drivers in alopecia areata: hair regrowth in a patient with <i>AIRE</i> gene mutation (autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy, APECED syndrome) treated with ruxolitinib
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Varicella Recurrence Complicated by Pneumonia After Liver Transplantation for APECED
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- BH02 Overcoming genetic drivers in alopecia areata: hair regrowth in a patient with the <i>AIRE</i> gene mutation treated with ruxolitinib
- Clinical case of alopecia totalis in pediatric practice
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- A Comparative study of Regulations of Cell and Gene therapy in US, EU and India