Found: 29
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Autoantibodies Neutralizing GM-CSF in HIV-Negative Colombian Patients Infected with Cryptococcus gattii and C. neoformans.
- Published in:
- Journal of Clinical Immunology, 2024, v. 44, n. 7, p. 1, doi. 10.1007/s10875-024-01757-y
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- Publication type:
- Article
Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency.
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- Journal of Clinical Immunology, 2024, v. 44, n. 3, p. 1, doi. 10.1007/s10875-024-01661-5
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- Publication type:
- Article
Autoantibodies Neutralizing Type I IFNs in the Bronchoalveolar Lavage of at Least 10% of Patients During Life-Threatening COVID-19 Pneumonia.
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- Journal of Clinical Immunology, 2023, v. 43, n. 6, p. 1093, doi. 10.1007/s10875-023-01512-9
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- Publication type:
- Article
Genetic inhibition of CARD9 accelerates the development of atherosclerosis in mice through CD36 dependent-defective autophagy.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40216-x
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- Publication type:
- Article
Anti-GM-CSF Neutralizing Autoantibodies in Colombian Patients with Disseminated Cryptococcosis.
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- Journal of Clinical Immunology, 2023, v. 43, n. 5, p. 921, doi. 10.1007/s10875-023-01451-5
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- Publication type:
- Article
Invasive Rhinosinusitis Caused by Alternaria infectoria in a Patient with Autosomal Recessive CARD9 Deficiency and a Review of the Literature.
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- Journal of Fungi, 2022, v. 8, n. 5, p. 446, doi. 10.3390/jof8050446
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- Article
Case Report: Invasive Cryptococcosis in French Guiana: Immune and Genetic Investigation in Six Non-HIV Patients.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.881352
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- Publication type:
- Article
CARD9 Expression Pattern, Gene Dosage, and Immunodeficiency Phenotype Revisited.
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- Journal of Clinical Immunology, 2022, v. 42, n. 2, p. 336, doi. 10.1007/s10875-021-01173-6
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- Publication type:
- Article
Case Report: A New Gain-of-Function Mutation of STAT1 Identified in a Patient With Chronic Mucocutaneous Candidiasis and Rosacea-Like Demodicosis: An Emerging Association.
- Published in:
- 2021
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- Publication type:
- Case Study
Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths.
- Published in:
- Science Immunology, 2021, v. 6, n. 62, p. 1, doi. 10.1126/sciimmunol.abl4340
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- Article
Case Report: Interleukin-2 Receptor Common Gamma Chain Defect Presented as a Hyper-IgE Syndrome.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.696350
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- Publication type:
- Article
Pediatric Demodicosis Associated with Gain-of-Function Variant in STAT1 Presenting as Rosacea-Type Rash.
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- 2021
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- Publication type:
- Letter
Functional analysis of two STAT1 gain-of-function mutations in two Iranian families with autosomal dominant chronic mucocutaneous candidiasis.
- Published in:
- Medical Mycology, 2021, v. 59, n. 2, p. 180, doi. 10.1093/mmy/myaa043
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- Publication type:
- Article
Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome.
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- Journal of Clinical Immunology, 2020, v. 40, n. 6, p. 807, doi. 10.1007/s10875-020-00803-9
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- Publication type:
- Article
Inherited CARD9 Deficiency in a Patient with Both Exophiala spinifera and Aspergillus nomius Severe Infections.
- Published in:
- Journal of Clinical Immunology, 2020, v. 40, n. 2, p. 359, doi. 10.1007/s10875-019-00740-2
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- Publication type:
- Article
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β.
- Published in:
- Science Immunology, 2019, v. 4, n. 41, p. 1, doi. 10.1126/sciimmunol.aax7965
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- Publication type:
- Article
Deficiency of Interleukin-1 Receptor Antagonist: A Case with Late Onset Severe Inflammatory Arthritis, Nail Psoriasis with Onychomycosis and Well Responsive to Adalimumab Therapy.
- Published in:
- Case Reports in Immunology, 2019, p. 1, doi. 10.1155/2019/1902817
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- Publication type:
- Article
A CARD9 Founder Mutation Disrupts NF-κB Signaling by Inhibiting BCL10 and MALT1 Recruitment and Signalosome Formation.
- Published in:
- Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.02366
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- Publication type:
- Article
Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies.
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- 2017
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- Publication type:
- Case Study
Visceral leishmaniasis in two patients with IL-12p40 and IL-12Rβ1 deficiencies.
- Published in:
- 2017
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- Publication type:
- journal article
Erratum to: Chronic and Invasive Fungal Infections in a Family with CARD9 Deficiency.
- Published in:
- 2016
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- Publication type:
- Erratum
Infectious diseases, autoimmunity and midline defect in a patient with a novel bi-allelic mutation in IL12RB1 gene.
- Published in:
- Turkish Journal of Pediatrics, 2016, v. 58, n. 3, p. 331
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- Publication type:
- Article
Chronic and Invasive Fungal Infections in a Family with CARD9 Deficiency.
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- Journal of Clinical Immunology, 2016, v. 36, n. 3, p. 204, doi. 10.1007/s10875-016-0255-8
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- Publication type:
- Article
A Homozygous CARD9 Mutation in a Brazilian Patient with Deep Dermatophytosis.
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- Journal of Clinical Immunology, 2015, v. 35, n. 5, p. 486, doi. 10.1007/s10875-015-0170-4
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- Publication type:
- Article
Inherited CARD9 Deficiency in 2 Unrelated Patients With Invasive Exophiala Infection.
- Published in:
- 2015
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- Publication type:
- Case Study
Tuberculin skin test negativity is under tight genetic control of chromosomal region 11p14-15 in settings with different tuberculosis endemicities.
- Published in:
- 2015
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- Publication type:
- journal article
Mycobacterium simiae Infection in Two Unrelated Patients with Different Forms of Inherited IFN-γR2 Deficiency.
- Published in:
- Journal of Clinical Immunology, 2014, v. 34, n. 8, p. 904, doi. 10.1007/s10875-014-0085-5
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- Publication type:
- Article
Association Study of Genes Controlling IL-12-dependent IFN-γ Immunity: STAT4 Alleles Increase Risk of Pulmonary Tuberculosis in Morocco.
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- Journal of Infectious Diseases, 2014, v. 210, n. 4, p. 611, doi. 10.1093/infdis/jiu140
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- Publication type:
- Article
Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease.
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- Human Molecular Genetics, 2013, v. 22, n. 4, p. 769, doi. 10.1093/hmg/dds484
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- Publication type:
- Article