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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
Inherited CARD9 Deficiency Due to a Founder Effect in East Asia.
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- Journal of Clinical Immunology, 2024, v. 44, n. 5, p. 1, doi. 10.1007/s10875-024-01724-7
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- Publication type:
- Article
Human autoantibodies neutralizing type I IFNs: From 1981 to 2023.
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- Immunological Reviews, 2024, v. 322, n. 1, p. 98, doi. 10.1111/imr.13304
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- Publication type:
- Article
Isolated Chronic Mucocutaneous Candidiasis due to a Novel Duplication Variant of IL17RC.
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- Journal of Clinical Immunology, 2024, v. 44, n. 1, p. 1, doi. 10.1007/s10875-023-01601-9
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- Publication type:
- Article
Severe acute herpes virus type 2 primo-infection and its association with anti-type 1 interferon autoantibodies.
- Published in:
- 2023
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- Publication type:
- Case Study
Inborn Errors of Immunity—the Sri Lankan Experience 2010–2022.
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- Journal of Clinical Immunology, 2023, v. 43, n. 8, p. 1858, doi. 10.1007/s10875-023-01542-3
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- Publication type:
- Article
Interventional pulmonary procedures and their outcomes in patients with STAT3 hyper IgE syndrome.
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- BMC Surgery, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12893-023-02193-2
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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
No increased prevalence of autoantibodies neutralizing type I IFNs in idiopathic pulmonary fibrosis patients.
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- Respiratory Research, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12931-023-02396-4
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- Publication type:
- Article
Immunocompromised Host Pneumonia: Definitions and Diagnostic Criteria: An Official American Thoracic Society Workshop Report.
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- Annals of the American Thoracic Society, 2023, v. 20, n. 3, p. 341, doi. 10.1513/AnnalsATS.202212-1019ST
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- Publication type:
- Article
IRAK1 Duplication in MECP2 Duplication Syndrome Does Not Increase Canonical NF-κB–Induced Inflammation.
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- Journal of Clinical Immunology, 2023, v. 43, n. 2, p. 421, doi. 10.1007/s10875-022-01390-7
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- Publication type:
- Article
Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1473, doi. 10.1007/s10875-022-01289-3
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- Publication type:
- Article
The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1508, doi. 10.1007/s10875-022-01352-z
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- Publication type:
- Article
Chronic Granulomatous Disease-Like Presentation of a Child with Autosomal Recessive PKCδ Deficiency.
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- Journal of Clinical Immunology, 2022, v. 42, n. 6, p. 1244, doi. 10.1007/s10875-022-01268-8
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- Publication type:
- Article
Notch, RORC and IL-23 signals cooperate to promote multi-lineage human innate lymphoid cell differentiation.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32089-3
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- Publication type:
- Article
Human T-bet governs the generation of a distinct subset of CD11c<sup>high</sup>CD21<sup>low</sup> B cells.
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- Science Immunology, 2022, v. 7, n. 73, p. 1, doi. 10.1126/sciimmunol.abq3277
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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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- Publication type:
- Article
Case Report: Invasive Cryptococcosis in French Guiana: Immune and Genetic Investigation in Six Non-HIV Patients.
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- 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
Biallelic TRAF3IP2 variants causing chronic mucocutaneous candidiasis in a child harboring a STAT1 variant.
- Published in:
- Pediatric Allergy & Immunology, 2021, v. 32, n. 8, p. 1804, doi. 10.1111/pai.13603
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- Publication type:
- Article
A Novel TRAF3IP2 Mutation Causing Chronic Mucocutaneous Candidiasis.
- Published in:
- 2021
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- Publication type:
- Letter
Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 5, p. 975, doi. 10.1007/s10875-021-00988-7
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- Publication type:
- 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
The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee.
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- Journal of Clinical Immunology, 2021, v. 41, n. 3, p. 666, doi. 10.1007/s10875-021-00980-1
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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
A new case of deep dermatophytic disease with inherited CARD9 deficiency.
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- International Journal of Dermatology, 2021, v. 60, n. 1, p. e15, doi. 10.1111/ijd.15294
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- Publication type:
- Article
IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation.
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- Journal of Clinical Immunology, 2021, v. 41, n. 1, p. 125, doi. 10.1007/s10875-020-00885-5
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- Publication type:
- Article
Human STAT1 Gain-of-Function Heterozygous Mutations: Chronic Mucocutaneous Candidiasis and Type I Interferonopathy.
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- Journal of Clinical Immunology, 2020, v. 40, n. 8, p. 1065, doi. 10.1007/s10875-020-00847-x
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- Publication type:
- Article
Disseminated Infectious Disease Caused by Histoplasma capsulatum in an Adult Patient as First Manifestation of Inherited IL-12Rβ1 Deficiency.
- Published in:
- 2020
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- Publication type:
- Letter
Anti-GM-CSF Autoantibodies and Cryptococcus neoformans var. grubii CNS Vasculitis.
- Published in:
- 2020
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- Publication type:
- Letter
Human inborn errors of immunity underlying superficial or invasive candidiasis.
- Published in:
- Human Genetics, 2020, v. 139, n. 6/7, p. 1011, doi. 10.1007/s00439-020-02141-7
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- Publication type:
- Article
The IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation.
- Published in:
- 2020
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- Publication type:
- Letter
Correction to: the IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic because of a Reinitiation of Translation.
- Published in:
- 2020
- By:
- Publication type:
- Correction Notice
Large-scale genome mining allows identification of neutral polymorphisms and novel resistance mutations in genes involved in Candida albicans resistance to azoles and echinocandins.
- Published in:
- 2020
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- Publication type:
- journal 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
Human BCL10 Deficiency due to Homozygosity for a Rare Allele.
- Published in:
- Journal of Clinical Immunology, 2020, v. 40, n. 2, p. 388, doi. 10.1007/s10875-020-00760-3
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- Publication type:
- Article
Efficacy of Dupilumab for Controlling Severe Atopic Dermatitis in a Patient with Hyper-IgE Syndrome.
- Published in:
- 2020
- By:
- Publication type:
- Letter
Aspergillus fumigatus Infection in Humans With STAT3-Deficiency Is Associated With Defective Interferon-Gamma and Th17 Responses.
- Published in:
- Frontiers in Immunology, 2020, p. 1, doi. 10.3389/fimmu.2020.00038
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- Publication type:
- Article
A 7-Year-Old Child With Headaches and Prolonged Fever Associated With Oral and Nail Lesions.
- Published in:
- Open Forum Infectious Diseases, 2019, v. 6, n. 11, p. N.PAG, doi. 10.1093/ofid/ofz229
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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
Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-34953-z
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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
Arid5a makes the IL-17A/F-responsive pathway less arid.
- Published in:
- Science Signaling, 2018, v. 11, n. 551, p. 1, doi. 10.1126/scisignal.aau8876
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- Publication type:
- Article
Inherited CARD9 Deficiency: Invasive Disease Caused by Ascomycete Fungi in Previously Healthy Children and Adults.
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 6, p. 656, doi. 10.1007/s10875-018-0539-2
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- Publication type:
- Article
Human hyper-IgE syndrome: singular or plural?
- Published in:
- Mammalian Genome, 2018, v. 29, n. 7/8, p. 603, doi. 10.1007/s00335-018-9767-2
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- Publication type:
- Article
A Clinical Presentation of IRAK-4 Deficiency.
- Published in:
- 2018
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- Publication type:
- Abstract
Exome sequencing reveals gain-offunction mutations in STAT1 conferring predisposition to chronic mucocutaneous candidiasis and tuberculosis in six Colombian patients.
- Published in:
- Revista Alergia de Mexico, 2018, v. 65, p. 114
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- Publication type:
- Article