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Trough Concentrations of Specific Antibodies in Primary Immunodeficiency Patients Receiving Intravenous Immunoglobulin Replacement Therapy.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 4, p. 592, doi. 10.3390/jcm10040592
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- Publication type:
- Article
RIPK1 mutations causing infantile-onset IBD with inflammatory and fistulizing features.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.1041315
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- Publication type:
- Article
GATA2 Deficiency in Adult Life Is Characterized by Phenotypic Diversity and Delayed Diagnosis.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.886117
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- Publication type:
- Article
Genetic workup as a complementary tool for the diagnosis of primary complement component deficiencies: a multicenter experience.
- Published in:
- European Journal of Pediatrics, 2022, v. 181, n. 5, p. 1997, doi. 10.1007/s00431-022-04397-9
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- Publication type:
- Article
Correlation between ' ACKR1/ DARC null' polymorphism and benign neutropenia in Yemenite Jews.
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- British Journal of Haematology, 2015, v. 170, n. 6, p. 892, doi. 10.1111/bjh.13345
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- Publication type:
- Article
B cell repertoire in patients with a novel BTK mutation: expanding the spectrum of atypical X-linked agammaglobulinemia.
- Published in:
- Immunologic Research, 2022, v. 70, n. 2, p. 216, doi. 10.1007/s12026-022-09263-2
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- Publication type:
- Article
Exploring genetic defects in adults who were clinically diagnosed as severe combined immune deficiency during infancy.
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- Immunologic Research, 2021, v. 69, n. 2, p. 145, doi. 10.1007/s12026-021-09179-3
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- Publication type:
- Article
A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia.
- Published in:
- Immunologic Research, 2021, v. 69, n. 1, p. 100, doi. 10.1007/s12026-021-09172-w
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- Publication type:
- Article
Immune reconstitution after HSCT in SCID—a cohort of conditioned and unconditioned patients.
- Published in:
- Immunologic Research, 2019, v. 67, n. 2/3, p. 166, doi. 10.1007/s12026-019-09081-z
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- Publication type:
- Article
MHC II deficient infant identified by newborn screening program for SCID.
- Published in:
- Immunologic Research, 2018, v. 66, n. 4, p. 537, doi. 10.1007/s12026-018-9019-2
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- Publication type:
- Article
Co-appearance of OPV and BCG vaccine-derived complications in two infants with severe combined immunodeficiency.
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- Immunologic Research, 2018, v. 66, n. 3, p. 437, doi. 10.1007/s12026-018-9007-6
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- Publication type:
- Article
First Year of Israeli Newborn Screening for Severe Combined Immunodeficiency-Clinical Achievements and Insights.
- Published in:
- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01448
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- Publication type:
- Article
The Kinetics of Early T and B Cell Immune Recovery after Bone Marrow Transplantation in RAG-2-Deficient SCID Patients.
- Published in:
- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0030494
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- Publication type:
- Article
The Effect of Gentamicin-Induced Readthrough on a Novel Premature Termination Codon of CD18 Leukocyte Adhesion Deficiency Patients.
- Published in:
- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0013659
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- Publication type:
- Article
G23D: Online tool for mapping and visualization of genomic variants on 3D protein structures.
- Published in:
- BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-3028-0
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- Publication type:
- Article
Alterations in T and B Cell Receptor Repertoires Patterns in Patients With IL10 Signaling Defects and History of Infantile-Onset IBD.
- Published in:
- Frontiers in Immunology, 2020, p. 1, doi. 10.3389/fimmu.2020.00109
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- Publication type:
- Article
Reduced Function and Diversity of T Cell Repertoire and Distinct Clinical Course in Patients With IL7RA Mutation.
- Published in:
- Frontiers in Immunology, 2019, p. 1, doi. 10.3389/fimmu.2019.01672
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- Publication type:
- Article
SARS-CoV-2 spike antibody concentration in gamma globulin products from high-prevalence COVID-19 countries are transmitted to X-linked agammaglobulinemia patients.
- Published in:
- Frontiers in Immunology, 2023, v. 14, p. 01, doi. 10.3389/fimmu.2023.1156823
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- Publication type:
- Article
Treatment options for DOCK8 deficiency‐related severe dermatitis.
- Published in:
- Journal of Dermatology, 2021, v. 48, n. 9, p. 1386, doi. 10.1111/1346-8138.15955
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- Publication type:
- Article
Chronic demodicosis in patients with immune dysregulation: An unexpected infectious manifestation of Signal transducer and activator of transcription (STAT)1 gain‐of‐function.
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- Clinical & Experimental Immunology, 2021, v. 206, n. 1, p. 56, doi. 10.1111/cei.13636
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- Publication type:
- Article
Timely and spatially regulated maturation of B and T cell repertoire during human fetal development.
- Published in:
- Science Translational Medicine, 2015, v. 7, n. 276, p. 1, doi. 10.1126/scitranslmed.aaa0072
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- Publication type:
- Article
Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK.
- Published in:
- Journal of Clinical Immunology, 2024, v. 44, n. 1, p. 1, doi. 10.1007/s10875-023-01614-4
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- Publication type:
- Article
SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related Lymphoma.
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- Journal of Clinical Immunology, 2023, v. 43, n. 3, p. 625, doi. 10.1007/s10875-022-01412-4
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- Publication type:
- Article
Inadequate Activation of γδT- and B-cells in Patient with Wiskott-Aldrich Syndrome (WAS) Portrayed by TRG and IGH Repertoire Analyses.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 1, p. 109, doi. 10.1007/s10875-022-01349-8
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- Publication type:
- Article
A Large Cohort of RAG1/2-Deficient SCID Patients—Clinical, Immunological, and Prognostic Analysis.
- Published in:
- Journal of Clinical Immunology, 2020, v. 40, n. 1, p. 211, doi. 10.1007/s10875-019-00717-1
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- Publication type:
- Article
Novel MALT1 Mutation Linked to Immunodeficiency, Immune Dysregulation, and an Abnormal T Cell Receptor Repertoire.
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- Journal of Clinical Immunology, 2019, v. 39, n. 4, p. 401, doi. 10.1007/s10875-019-00629-0
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- Publication type:
- Article
Correction to: Novel Mutations in RASGRP1 Are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma.
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- 2018
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- Publication type:
- Correction Notice
Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma.
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 6, p. 699, doi. 10.1007/s10875-018-0533-8
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- Publication type:
- Article
A Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF).
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 8, p. 801, doi. 10.1007/s10875-016-0340-z
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- Publication type:
- Article
Disturbed B and T cell homeostasis and neogenesis in patients with ataxia telangiectasia.
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- Journal of Clinical Immunology, 2014, v. 34, n. 5, p. 561, doi. 10.1007/s10875-014-0044-1
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- Publication type:
- Article
Novel SMARCAL1 Bi-allelic Mutations Associated with a Chromosomal Breakage Phenotype in a Severe SIOD Patient.
- Published in:
- Journal of Clinical Immunology, 2014, v. 34, n. 1, p. 76, doi. 10.1007/s10875-013-9957-3
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- Publication type:
- Article
T-Cell Compartment in Synovial Fluid of Pediatric Patients with JIA Correlates with Disease Phenotype.
- Published in:
- Journal of Clinical Immunology, 2011, v. 31, n. 6, p. 1021, doi. 10.1007/s10875-011-9580-0
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- Publication type:
- Article
The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation.
- Published in:
- Immunologic Research, 2017, v. 65, n. 3, p. 651, doi. 10.1007/s12026-016-8883-x
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- Publication type:
- Article
Combined immunodeficiency in a patient with mosaic monosomy 21.
- Published in:
- Immunologic Research, 2016, v. 64, n. 4, p. 841, doi. 10.1007/s12026-016-8803-0
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- Publication type:
- Article
Highlighting the problematic reliance on CD18 for diagnosing leukocyte adhesion deficiency type 1.
- Published in:
- Immunologic Research, 2016, v. 64, n. 2, p. 476, doi. 10.1007/s12026-015-8706-5
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- Publication type:
- Article
Insight into normal thymic activity by assessment of peripheral blood samples.
- Published in:
- Immunologic Research, 2015, v. 61, n. 3, p. 198, doi. 10.1007/s12026-014-8558-4
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- Publication type:
- Article
Purine nucleoside phosphorylase deficiency presenting as severe combined immune deficiency.
- Published in:
- Immunologic Research, 2013, v. 56, n. 1, p. 150, doi. 10.1007/s12026-012-8380-9
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- Publication type:
- Article
Congenital neutropenia with variable clinical presentation in novel mutation of the SRP54 gene.
- Published in:
- 2020
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- Publication type:
- journal article
Quantification of specific T and B cells immunological markers in children with chronic and transient ITP.
- Published in:
- 2017
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- Publication type:
- journal article
Characterizing T Cells in SCID Patients Presenting with Reactive or Residual T Lymphocytes.
- Published in:
- Clinical & Developmental Immunology, 2012, p. 1, doi. 10.1155/2012/261470
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- Publication type:
- Article
Thymus Activity, Vitamin D, and Respiratory Infections in Adolescent Swimmers.
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- Israel Medical Association Journal, 2015, v. 17, n. 9, p. 571
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- Publication type:
- Article
Newborn Screening for Severe T and B cell Immunodeficiency in Israel: a Pilot Study.
- Published in:
- Israel Medical Association Journal, 2013, v. 15, n. 8, p. 404
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- Publication type:
- Article
Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells.
- Published in:
- 2020
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- Publication type:
- Correction Notice
Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-14809-9
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- Publication type:
- Article