Disease: Autoimmune polyglandular syndrome type 1
- A 20-year study of autoimmune polyendocrine syndrome type II and III in Taiwan
- A Case of Autoimmune Poly Glandular Glandular Syndrome Type 2 (Schmidt's Syndrome)
- A case of multiple endocrine neoplasia syndrome type 2A combined with autoimmune polyendocrine syndrome type
- A case of multiple endocrine neoplasia syndrome type 2A combined with autoimmune polyendocrine syndrome type Ⅲ
- A case report of anti-GAD65 antibody-positive autoimmune encephalitis in children associated with autoimmune polyendocrine syndrome type-II and literature review
- A non-classical presentation of APECED in a family with heterozygous R203X AIRE gene mutation
- A novel missense mutation in the AIRE gene underlying autoimmune polyglandular syndrome type 1
- A partial form of AIRE deficiency underlies a mild form of autoimmune polyendocrine syndrome type 1
- A Rare Case of Autoimmune Enteropathy Associated with Autoimmune Hepatitis
- A Systematic Review of Autoimmune Oophoritis Therapies
- Adolescent onset of autoimmune polyglandular syndrome type 2
- Adrenal crisis prompted by SARS-CoV-2 infection in a patient with autoimmune polyglandular syndrome type 1 (APS type 1)
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Alopecia areata and occurrence of vitiligo and hypothyroidism in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients
- An 11-year-old girl with Autoimmune Polyglandular Syndrome (APS) type 2: a case report and review of literature
- An uncommon presentation of autoimmune polyglandular syndrome type 1 (APS-1)-A case report
- Analysis of a series of Italian APECED patients with autoimmune hepatitis and gastro-enteropathies
- Analysis of the AIRE Gene Promoter in Patients Affected by Autoimmune Polyendocrine Syndromes
- APECED and the place of AIRE in the puzzle of the immune network associated with autoimmunity
- APECED Rash as the First Manifestation of APECED Syndrome
- Association of latent autoimmune diabetes of adults with type 3 polyglandular autoimmune syndrome-a diagnostic challenge
- Autoantibody repertoire characterization provides insight into the pathogenesis of monogenic and polygenic autoimmune diseases
- Autoimmune adrenal insufficiency in children: a hint for polyglandular syndrome type 2?
- Autoimmune amelogenesis imperfecta in patients with APS-1 and coeliac disease
- Autoimmune enteropathy complicated with primary biliary cholangitis
- Autoimmune polyendocrine syndrome in adults. Focus on rheumatological aspects of the problem: A review
- Autoimmune polyendocrine syndrome type 1: Clinical manifestations, pathogenetic features, and management approach
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) and esophageal rupture by candida infection: A case report and review
- Autoimmune Polyglandular Syndrome Type 1: A Report of Rare Case of a 16-Year-Old Asian Female Patient With Respiratory Manifestations
- Autoimmune Polyglandular Syndrome Type 3 Complicated with IgG4-related Disease
- Autoimmune polyglandular syndrome type 3 diagnosed with cerebral venous sinus thrombosis: a case report
- Autoimmune polyglandular syndrome type 4: experience from a single reference center
- Autoimmune Polyglandular Syndrome Type II: A Case Report
- Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance
- Autoimmune polyglandular syndrome with shock and high anion gap metabolic acidosis
- Autoimmune regulator (Aire) deficiency results in reduced memory CD8(+) T cells after Listeria monocytogenes infection in a murine model
- Autoimmune regulator (Aire) deficiency results in reduced memory CD8<sup>+</sup> T cells after Listeria monocytogenes infection in a murine model
- Autoimmune regulator (AIRE): Takes a hypoxia-inducing factor 1A (HIF1A) route to regulate FOXP3 expression in PCOS
- Bone Tissue Evaluation Indicates Abnormal Mineralization in Patients with Autoimmune Polyendocrine Syndrome Type I: Report on Three Cases
- Case 29-2022: A 33-Year-Old Man with Chronic Diarrhea and Autoimmune Enteropathy
- Case report: Discovery of a <em>de novo FAM111B</em> pathogenic variant in a patient with an APECED-like clinical phenotype
- Case report: Virus-induced hemophagocytic lymphohistiocytosis in a patient with APECED
- Challenges in autoimmune polyendocrine syndrome type 2 with the full triad induced by anti-programmed cell death 1: a case report and review of the literature
- Characterisation of APS-1 Experimental Models Is Crucial for Development of Novel Therapies
- Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China-expanding the atypical phenotypes
- Clinical characteristics and management of autoimmune enteropathy in children: case reports and literature review
- Clinical manifestations, diagnosis and long-term prognosis of adult autoimmune enteropathy: Experience from Peking Union Medical College Hospital
- Cone dystrophy associated with autoimmune polyglandular syndrome type 1
- Decreased T-cell response against latent cytomegalovirus infection does not correlate with anti-IFN autoantibodies in patients with APECED
- Differentiation of Pluripotent Stem Cells Into Thymic Epithelial Cells and Generation of Thymic Organoids: Applications for Therapeutic Strategies Against APECED
- Dysregulated germinal center reaction with expanded T follicular helper cells in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy lymph nodes
- Endogenous ocular nocardiosis in an immunosupressed patient with autoimmune enteropathy
- Epigenetic and immunological indicators of IPEX disease in subjects with FOXP3 gene mutation
- Evaluation of a large set of patients with Autoimmune Polyglandular Syndrome from a single reference centre in context of different classifications
- Exploring Chronic Hypocalcemia: Insights into Autoimmune Polyglandular Syndrome Type 1-A Case Study and Literature Review
- Extrathymic expression of Aire controls the induction of effective T<sub>H</sub>17 cell-mediated immune response to Candida albicans
- FOXP3 deficiency, from the mechanisms of the disease to curative strategies
- Genetic Diagnosis Guides Treatment of Autoimmune Enteropathy
- Human autoantibodies neutralizing type I IFNs: From 1981 to 2023
- Identification of <em>AIRE</em> pathogenic variants ends diagnostic odyssey for Saudi child with infantile-onset keratoconjunctivitis as an early sign of autoimmune polyglandular syndrome type1; a case report
- Identification of AIRE pathogenic variants ends diagnostic odyssey for Saudi child with infantile-onset keratoconjunctivitis as an early sign of autoimmune polyglandular syndrome type1; a case report
- Identification of unstable regulatory and autoreactive effector T cells that are expanded in patients with <em>FOXP3</em> mutations
- Immune dysregulation, polyendocrinopathy and enteropathy, X-linked (IPEX) syndrome due to a mutation in FOXP3, modified by a pathogenic variant in SON (SON DNA-binding protein)
- Immunological Evaluation of Pediatric Patients with Polyautoimmunity
- Increased frequency of microalbuminuria in patients with type 3 autoimmune polyglandular syndrome (APS) compared to isolated autoimmune type 1 diabetes mellitus: A real-life study
- Increased type 1 inflammation in gynecologic cervicovaginal samples in patients with APS-1
- Initiation of Continuous rhPTH Infusion With Insulin Pump in an Inpatient Setting
- Interleukin (IL)-23, IL-31, and IL-33 Play a Role in the Course of Autoimmune Endocrine Diseases
- IPEX syndrome from diagnosis to cure, learning along the way
- JAK Inhibition Immunotherapy for APS-1
- Just Anorexia?
- Learning the Autoimmune Pathogenesis Through the Study of Aire
- Leber congenital amaurosis as the initial and essential manifestation in a Chinese patient with autoimmune polyglandular syndrome Type 1
- Long-term remission of candidiasis with fermented lingonberry mouth rinse in an adult patient with APECED
- Multiple endocrine neoplasia type 2 and autoimmune polyendocrine syndromes (type 1 diabetes mellitus and Graves' disease) in a 16-year-old male with Kabuki syndrome
- Neurological Diseases and Prevalence of Antineuronal Antibodies in Patients with Autoimmune Polyendocrine Syndrome Type 1 - A National Cohort Study
- Non-infectious gastrointestinal manifestations of Good syndrome
- Novel Insights into the Autoimmunity from the Genetic Approach of the Human Disease
- Ocular features of autoimmune polyendocrinopathy candidiasis ectodermal dystrophy
- Ocular Sarcoidosis and Autoimmune Polyglandular Syndrome Type 2: A Case Report
- P450 Side-Chain Cleavage Enzyme (P450-SCC) Is an Ovarian Autoantigen in a Mouse Model for Autoimmune Oophoritis
- Polyendocrine syndromes in dogs
- Polyglandular Autoimmune Syndrome Type I
- Polyglandular Autoimmune Syndrome Type I
- Progressive Impairment of Prepubertal Growth in Children With APECED
- Pubertal development and hypogonadism in males with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: a retrospective study
- Recurrent Hypokalemia and Adrenal Steroids in Patients With APECED
- Recurrent venous thrombosis - an unusual first presentation of autoimmune polyendocrinopathy syndrome type 3B
- Revisiting Genetic Testing for Patients with Negative Results: IPEX and FOXP3
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- SARS-CoV-2-induced adrenal crisis in a patient with autoimmune polyglandular syndrome type 1: case report
- Secondary membranous nephropathy associated to autoimmune polyglandular syndrome Type II
- Successful live birth following a short course of glucocorticoid suppression in a patient with autoimmune polyglandular syndrome type 2 and premature ovarian insufficiency: A case report
- Systemic interferon type I and B cell responses are impaired in autoimmune polyendocrine syndrome type 1
- T-cell receptor repertoire analysis of CD4-positive T cells from blood and an affected organ in an autoimmune mouse model
- The Role of Interferon-gamma in Autoimmune Polyendocrine Syndrome Type 1
- Two children of autoimmune enteropathy
- Type 3 autoimmune polyglandular syndrome (APS-3) or type 3 multiple autoimmune syndrome (MAS-3): an expanding galaxy
- Unusual Manifestations of APECED
- VKH with APECED in a Two-Year-Old Child: A Rare Concomitant Diagnosis in an Unprecedented Age