Works matching DE "AUTOINFLAMMATORY diseases"
Results: 552
Include rare, treatable IL-1-mediated autoinflammatory diseases in differential diagnosis of chronic or periodic inflammation.
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- Drugs & Therapy Perspectives, 2024, v. 40, n. 9, p. 353, doi. 10.1007/s40267-024-01096-3
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- Article
A Tailored Artificial DNase Blocks Sensor Activation and Prevents Autoimmune and Autoinflammatory Diseases.
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- Advanced Functional Materials, 2023, v. 33, n. 19, p. 1, doi. 10.1002/adfm.202213465
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- Article
Structural impacts of two disease-linked ADAR1 mutants: a molecular dynamics study.
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- Journal of Computer-Aided Molecular Design, 2024, v. 38, n. 1, p. 1, doi. 10.1007/s10822-024-00565-1
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- Article
Spiculated lung infiltrate mimicking actinomycosis in adult-onset Still's disease complicated by macrophage activation syndrome.
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- Rheumatology Forum, 2023, v. 9, n. 1, p. 36, doi. 10.5603/RF.2023.0007
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Gastrointestinal endoscopic findings of autoimmune and autoinflammatory diseases in pediatric rheumatology patients.
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- Northern Clinics of Istanbul, 2023, v. 10, n. 2, p. 228, doi. 10.14744/nci.2021.62713
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Course of COVID-19 in patients carrying different MEFV mutations of familial Mediterranean fever.
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- Medicine Science, 2024, v. 13, n. 2, p. 250, doi. 10.5455/medscience.2023.11.217
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- Article
The Clinical Characteristics and Prognosis of Exon 2 Mutations in Familial Mediterranean Fever.
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- European Journal of Therapeutics, 2023, v. 29, n. 3, p. 450, doi. 10.58600/eurjther1739
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- Article
Factors affecting patient-acceptable symptom states and treatment decision in familial Mediterranean fever.
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- Turkish Journal of Medical Sciences, 2022, v. 52, n. 6, p. 1991, doi. 10.55730/1300-0144.5547
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- Article
Non-adherence to colchicine treatment is a common misevaluation in familial Mediterranean fever.
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- Turkish Journal of Medical Sciences, 2021, v. 51, n. 5, p. 2357, doi. 10.3906/sag-2102-328
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- Article
MEFV mutation frequencies in a Turkish cohort with low prevalence of familial Mediterranean fever.
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- Turkish Journal of Medical Sciences, 2021, v. 51, n. 4, p. 1702, doi. 10.3906/sag-2009-119
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Phenotypic characterization of Familial Mediterranean Fever patients harboring variants of uncertain significance.
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- Turkish Journal of Medical Sciences, 2021, v. 51, n. 4, p. 1694, doi. 10.3906/sag-2011-273
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- Article
Autoinflammation in Syndromic Hidradenitis Suppurativa: The Role of AIM2.
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- Vaccines, 2023, v. 11, n. 1, p. 162, doi. 10.3390/vaccines11010162
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- Article
Current Evidence on Vaccinations in Pediatric and Adult Patients with Systemic Autoinflammatory Diseases.
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- Vaccines, 2023, v. 11, n. 1, p. 151, doi. 10.3390/vaccines11010151
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Evaluation of fetal cardiac morphology and functions in pregnant women with familial Mediterranean fever.
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- Echocardiography, 2022, v. 39, n. 4, p. 606, doi. 10.1111/echo.15336
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MVK, NLRP3, TNFRSF1A and MEFV gene mutation distributions in childhood autoinflammatory diseases: Experiences in North Anatolia.
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- Journal of Experimental & Clinical Medicine / Deneysel ve Klinik Tip Dergisi, 2023, v. 40, n. 4, p. 681, doi. 10.52142/omujecm.40.4.3
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- Article
Schnitzler Syndrome: Insights into Its Pathogenesis, Clinical Manifestations, and Current Management.
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- Biomolecules (2218-273X), 2024, v. 14, n. 6, p. 646, doi. 10.3390/biom14060646
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- Article
Patients with Systemic Juvenile Idiopathic Arthritis (SJIA) Show Differences in Autoantibody Signatures Based on Disease Activity.
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- Biomolecules (2218-273X), 2023, v. 13, n. 9, p. 1392, doi. 10.3390/biom13091392
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Activation and Pharmacological Regulation of Inflammasomes.
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- Biomolecules (2218-273X), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/biom12071005
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Platelets-related signature based diagnostic model in rheumatoid arthritis using WGCNA and machine learning.
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1204652
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- Article
Editorial: Women in autoimmune and autoinflammatory disorders.
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1222776
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- Article
Crosstalk between cholesterol metabolism and psoriatic inflammation.
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1124786
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The first successful bone marrow transplantation in Vietnam for a young Vietnamese boy with chronic granulomatous disease: a case report.
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1134852
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- Article
Case report: Schnitzler-like syndrome without monoclonal gammopathy.
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- Frontiers in Immunology, 2023, v. 14, p. 1, doi. 10.3389/fimmu.2023.1166620
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- Article
Single-cell transcriptomic analysis in two patients with rare systemic autoinflammatory diseases treated with anti-TNF therapy.
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- Frontiers in Immunology, 2023, v. 14, p. 1, doi. 10.3389/fimmu.2023.1091336
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Editorial: A new frontier in translational research on autoinflammatory diseases - various aspects of innate immunity on human diseases.
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- Frontiers in Immunology, 2023, v. 14, p. 1, doi. 10.3389/fimmu.2023.1147202
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Molecular interactions of adaptor protein PSTPIP2 control neutrophil-mediated responses leading to autoinflammation.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.1035226
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NLRP3 inflammasome and NLRP3-related autoinflammatory diseases: From cryopyrin function to targeted therapies.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.1007705
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Safety and efficacy of fecal microbiota transplantation for autoimmune diseases and autoinflammatory diseases: A systematic review and meta-analysis.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.944387
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A rapid turnaround gene panel for severe autoinflammation: Genetic results within 48 hours.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.998967
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Blau syndrome: Lessons learned in a tertiary care centre at Chandigarh, North India.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.932919
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Three Chinese pedigrees of A20 haploinsufficiency: clinical, cytokine and molecular characterization.
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- Frontiers in Immunology, 2022, v. 13, p. 01, doi. 10.3389/fimmu.2022.955079
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Interleukin-6 inhibition in the treatment of autoinflammatory diseases.
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- Frontiers in Immunology, 2022, v. 13, p. 01, doi. 10.3389/fimmu.2022.956795
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UVB-Induced Skin Autoinflammation Due to Nlrp1b Mutation and Its Inhibition by Anti-IL-1β Antibody.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.876390
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Case Report: Tocilizumab Treatment for VEXAS Syndrome With Relapsing Polychondritis: A Single-Center, 1-Year Longitudinal Observational Study In Japan.
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- 2022
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- Case Study
Modulation of Autoimmune and Autoinflammatory Diseases by Gasdermins.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.841729
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Nutcracker syndrome: a potentially underdiagnosed cause of proteinuria in children with familial Mediterranean fever.
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- Pediatric Nephrology, 2022, v. 37, n. 7, p. 1615, doi. 10.1007/s00467-021-05337-9
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- Article
Are autoimmune diseases autoinflammatory: Is it time to change the paradigm?
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- Lupus, 2021, v. 30, n. 11, p. 1722, doi. 10.1177/09612033211038931
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Hearing loss as the main clinical presentation in NLRP3-associated autoinflammatory disease.
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- Journal of Hearing Science, 2024, v. 14, n. 3, p. 128
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Biomaterials Functionalized with Inflammasome Inhibitors—Premises and Perspectives.
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- Journal of Functional Biomaterials, 2024, v. 15, n. 2, p. 32, doi. 10.3390/jfb15020032
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- Article
Constitutively active Lyn kinase causes a cutaneous small vessel vasculitis and liver fibrosis syndrome.
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- Nature Communications, 2023, v. 14, p. 1, doi. 10.1038/s41467-023-36941-y
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- Article
Erysipelas-like Erythema: A Pathognomonic Rash in Children with Familial Mediterranean Fever.
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- Medical Journal of Bakirkoy, 2023, v. 19, n. 2, p. 217, doi. 10.4274/BMJ.galenos.2023.2023.3-23
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- Article
Erysipelas-like Erythema: A Pathognomonic Rash in Children with Familial Mediterranean Fever.
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- Medical Journal of Bakirkoy, 2023, v. 19, n. 2, p. 217, doi. 10.4274/BMJ.galenos.2023.2023.3-23
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- Article
Analysis of Endotheal Nitric Oxide Synthase Gene VNTR Variant in Turkish FMF Patients.
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- Medical Journal of Bakirkoy, 2022, v. 18, n. 4, p. 433, doi. 10.4274/BMJ.galenos.2022.2022.5-7
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Clinical Characteristics and Short-term Outcomes of Paediatric Patients with Chronic Recurrent Multifocal Osteomyelitis.
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- Journal of the Child / Çocuk Dergisi, 2023, v. 23, n. 4, p. 334, doi. 10.26650/jchild.2023.1253446
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- Article
Blau Syndrome: Challenging Molecular Genetic Diagnostics of Autoinflammatory Disease.
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- Genes, 2024, v. 15, n. 6, p. 799, doi. 10.3390/genes15060799
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Predictive Clinical and Biological Criteria for Gene Panel Positivity in Suspected Inherited Autoinflammatory Diseases: Insights from a Case–Control Study.
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- Genes, 2023, v. 14, n. 10, p. 1939, doi. 10.3390/genes14101939
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Genetics of Generalized Pustular Psoriasis: Current Understanding and Implications for Future Therapeutics.
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- Genes, 2023, v. 14, n. 6, p. 1297, doi. 10.3390/genes14061297
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IN MEMORIAM PROFESSOR ANNAMARI RANKI.
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- Acta Dermato-Venereologica, 2024, v. 104, p. 1, doi. 10.2340/actadv.v104.40151
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- Article
ILSpectrum of Genetic Autoinflammatory Diseases Presenting with Cutaneous Symptoms.
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- Acta Dermato-Venereologica, 2020, v. 100, p. 140, doi. 10.2340/00015555-3427
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Acquired Cold Urticaria vs. Autoinflammatory Diseases, Genetic and Clinical Profile and Differential Diagnosis: Study of a Cohort of Patients in a Tertiary Reference Centre.
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- Acta Dermato-Venereologica, 2019, v. 99, n. 12, p. 1071, doi. 10.2340/00015555-3292
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- Article