Works matching DE "PRIMARY immunodeficiency diseases"
Results: 892
Cross-talk between immune cells and tumor cells in non-Hodgkin lymphomas arising in common variable immunodeficiency.
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- Expert Review of Clinical Immunology, 2024, v. 20, n. 12, p. 1461, doi. 10.1080/1744666X.2024.2398546
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- Article
Epstein–Barr virus-driven lymphoproliferation in inborn errors of immunity: a diagnostic and therapeutic challenge.
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- Expert Review of Clinical Immunology, 2024, v. 20, n. 11, p. 1331, doi. 10.1080/1744666X.2024.2386427
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- Article
The multidisciplinary approach to diagnosing inborn errors of immunity: a comprehensive review of discipline-based manifestations.
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- Expert Review of Clinical Immunology, 2024, v. 20, n. 10, p. 1237, doi. 10.1080/1744666X.2024.2372335
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- Article
The examination of family functioning in immunodeficiency patients in the context of McMaster family therapy in Turkey.
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- Asia Pacific Journal of Social Work & Development (Taylor & Francis Ltd), 2024, v. 34, n. 1, p. 51, doi. 10.1080/02185385.2022.2155232
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- Article
Predominantly antibody deficiencies: An important underlying cause of recurrent pneumonia in adults.
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- Canadian Journal of Respiratory, Critical Care, & Sleep Medicine, 2024, v. 8, n. 6, p. 270, doi. 10.1080/24745332.2024.2407787
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- Article
Safety and efficacy of a novel mini‐pool intravenous immunoglobulin therapy in children with primary immunodeficiency.
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- Vox Sanguinis, 2025, v. 120, n. 2, p. 140, doi. 10.1111/vox.13769
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- Article
I just hurt myself out in the garden... right?
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- Breathe, 2025, v. 21, n. 1, p. 1, doi. 10.1183/20734735.0179-2024
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- Article
Clinical Characterization and Mutation Analysis of 13 Iranian Ataxia Telangiectasia Patients: Introducing Two Novel Mutations.
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- Iranian Journal of Allergy, Asthma & Immunology, 2025, v. 24, n. 2, p. 187, doi. 10.18502/ijaai.v24i2.18147
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- Article
Comparación de las manifestaciones cutáneas de pacientes pediátricos con dermatitis atópica con las de pacientes con inmunodeficiencias primarias.
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- Revista Mexicana de Pediatria, 2024, v. 91, n. 3, p. 92, doi. 10.35366/119372
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- Article
Tests diagnostiques de la malabsorption digestive : indications et interprétations.
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- Hépato-Gastro & Oncologie Digestive, 2025, v. 32, n. 2, p. 161, doi. 10.1684/hpg.2025.2935
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- Article
Errores innatos de la inmunidad.
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- Acta Médica del Centro, 2024, v. 18, n. 4, p. 1
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- Article
DR SPUR'S MYSTERY CASE: The case of the chicken or is it the egg?
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- Current Allergy & Clinical Immunology, 2025, v. 38, n. 1, p. 60
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- Article
Editorial: Community series in primary immunodeficiencies worldwide, volume II.
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- Frontiers in Immunology, 2025, p. 1, doi. 10.3389/fimmu.2025.1564959
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The genetics of hyper IgE syndromes.
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- Frontiers in Immunology, 2025, p. 1, doi. 10.3389/fimmu.2025.1516068
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- Article
Living with primary immunodeficiency disease during the Covid-19 pandemic.
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- Journal of Public Health: From Theory to Practice (2198-1833), 2022, v. 30, n. 12, p. 2753, doi. 10.1007/s10389-021-01545-7
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- Article
Patient-centered outcomes with subcutaneous immunoglobulin use for infection control in primary and secondary immunodeficiencies: data of a GEIE Spanish Registry.
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- Frontiers in Immunology, 2025, p. 1, doi. 10.3389/fimmu.2025.1532367
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- Article
Integrated Metabolomic and Transcriptomic Analysis Revealed the Mechanism of BHPF Exposure in Endometrium.
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- Toxics, 2025, v. 13, n. 2, p. 100, doi. 10.3390/toxics13020100
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X-Linked CGD Chorioretinitis in Two Young Girls.
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- Biomedicines, 2025, v. 13, n. 2, p. 323, doi. 10.3390/biomedicines13020323
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Childhood-onset Takayasu arteritis and immunodeficiency: case-based review.
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- 2022
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- Case Study
Reducing Delays in Diagnosing Primary Immunodeficiency Through the Development and Implementation of a Clinical Decision Support Tool: Protocol for a Quality Improvement Project.
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- JMIR Research Protocols, 2022, v. 11, n. 1, p. 1, doi. 10.2196/32635
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- Article
Hypersensitivity Pneumonia Due to Lentil Aspiration: A Rare but Painstaking Pulmonary Illness.
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- Global Pediatric Health, 2024, p. 1, doi. 10.1177/2333794X241304580
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- Article
Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylation.
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- Human Genetics, 2022, v. 141, n. 7, p. 1279, doi. 10.1007/s00439-021-02400-1
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- Article
HDAC inhibition delays photoreceptor loss in Pde6b mutant mice of retinitis pigmentosa: insights from scRNA-seq and CUT&Tag.
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- PeerJ, 2023, p. 1, doi. 10.7717/peerj.15659
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- Article
Pulmonary Complications of Monogenic Patients with Common Variable Immunodeficiency: COVID-19 Perspectives.
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- Turkish Journal of Immunology, 2024, v. 12, p. 71, doi. 10.4274/tji.galenos.2023.08860
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- Article
Tracing the Spectrum of Inborn Errors of Immunity from Past to Present.
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- Turkish Journal of Immunology, 2024, v. 12, p. 1, doi. 10.4274/tji.galenos.2024.00001
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- Article
Primer İmmün Yetersizliklerde Western Blot Yönteminin Önemi: İki Aile Olgusundan Örnekler.
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- Turkish Journal of Immunology, 2019, v. 7, n. 3, p. 120, doi. 10.25002/tji.2019.1178
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- Article
Clinical Manifestations in the Patients with Primary Immunodeficiencies: Data from One Regional Center.
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- Turkish Journal of Immunology, 2019, v. 7, n. 3, p. 113, doi. 10.25002/tji.2019.1168
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- Article
Inmunodeficiencias primarias por déficit de IgA. Heterogeneidad clínica y reto diagnóstico.
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- Revista de Ciencias Médicas de Pinar del Río, 2023, v. 27, p. 1
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- Article
Severe Combined Immunodeficiency in Malaysia: It's Time to Shape a Future with No-One Left Behind.
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- Malaysian Journal of Medicine & Health Sciences, 2023, v. 19, n. 6, p. 1, doi. 10.47836/mjmhs.19.6.1
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- Article
Severe Combined Immunodeficiency Disease with Features of Haemophagocytic Lymphohistiocytosis: A Case Report.
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- 2021
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- Case Study
Salt Losing Crisis, Deep-seated Abscess and BCG Lymphadenitis in an Infant with Chronic Granulomatous Disease.
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- 2021
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- Case Study
Diagnostic Approach and Treatment of Severe Combined Immunodeficiency.
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- Malaysian Journal of Medicine & Health Sciences, 2021, v. 17, p. 176
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- Article
IgG replacement in multiple myeloma.
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- Blood Cancer Journal, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41408-024-01107-6
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- Article
A new-disease-causing dominant-negative variant in CARD11 gene in a Chinese case with recurrent fever.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-71673-z
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- Article
Revealing disease subtypes and heterogeneity in common variable immunodeficiency through transcriptomic analysis.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-74728-3
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- Article
Rare Variants in Primary Immunodeficiency Genes and Their Functional Partners in Severe COVID-19.
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- Biomolecules (2218-273X), 2023, v. 13, n. 9, p. 1380, doi. 10.3390/biom13091380
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- Article
Co-Stimulatory Molecules during Immune Control of Epstein Barr Virus Infection.
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- Biomolecules (2218-273X), 2022, v. 12, n. 1, p. 38, doi. 10.3390/biom12010038
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- Article
Genomic testing identifies monogenic causes in patients with very early-onset inflammatory bowel disease: a multicenter survey in an Iranian cohort.
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- Clinical & Experimental Immunology, 2024, v. 217, n. 1, p. 1, doi. 10.1093/cei/uxae037
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- Article
Clinical and experimental treatment of primary humoral immunodeficiencies.
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- Clinical & Experimental Immunology, 2024, v. 216, n. 2, p. 120, doi. 10.1093/cei/uxae008
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- Article
X-linked chronic granulomatous disease secondary to skewed X-chromosome inactivation in female patients.
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- Clinical & Experimental Immunology, 2024, v. 215, n. 3, p. 261, doi. 10.1093/cei/uxad129
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- Article
Not too little, not too much: the impact of mutation types in Wiskott-Aldrich syndrome and RAC2 patients.
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- Clinical & Experimental Immunology, 2023, v. 212, n. 2, p. 137, doi. 10.1093/cei/uxad001
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- Article
Inborn errors of human IKAROS: LOF and GOF variants associated with primary immunodeficiency.
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- Clinical & Experimental Immunology, 2023, v. 212, n. 2, p. 129, doi. 10.1093/cei/uxac109
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- Article
Identification of novel NFKB1 and ICOS frameshift variants in patients with CVID.
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- Clinical & Experimental Immunology, 2023, v. 211, n. 1, p. 68, doi. 10.1093/cei/uxac121
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- Article
Long-term efficacy, safety, and tolerability of a subcutaneous immunoglobulin 16.5% (cutaquig<sup>®</sup>) in the treatment of patients with primary immunodeficiencies.
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- Clinical & Experimental Immunology, 2022, v. 210, n. 2, p. 91, doi. 10.1093/cei/uxac092
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- Article
British Society for Immunology and United Kingdom Primary Immunodeficiency Network (UKPIN) consensus guideline for the management of immunoglobulin replacement therapy.
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- Clinical & Experimental Immunology, 2022, v. 210, n. 1, p. 1, doi. 10.1093/cei/uxac070
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Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK.
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- Clinical & Experimental Immunology, 2022, v. 209, n. 3, p. 247, doi. 10.1093/cei/uxac008
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Droplet digital PCR for identifying copy number variations in patients with primary immunodeficiency disorders.
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- Clinical & Experimental Immunology, 2022, v. 207, n. 3, p. 329, doi. 10.1093/cei/uxab034
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Diagnosis of HLH: two siblings, two distinct genetic causes.
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- Clinical & Experimental Immunology, 2022, v. 207, n. 2, p. 205, doi. 10.1093/cei/uxab019
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- Article
A single‐center pilot study in Malaysia on the clinical utility of whole‐exome sequencing for inborn errors of immunity.
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- Clinical & Experimental Immunology, 2021, v. 206, n. 2, p. 119, doi. 10.1111/cei.13626
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Clinical and laboratory findings in patients with leukocyte adhesion deficiency type I: A multicenter study in Turkey.
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- Clinical & Experimental Immunology, 2021, v. 206, n. 1, p. 47, doi. 10.1111/cei.13645
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- Article