80 results on '"Sullivan, Kathleen"'
Search Results
2. Kagami Ogata syndrome: a small deletion refines critical region for imprinting
3. Immune urinary biomarkers predict infant cardiac surgery-associated acute kidney injury
4. COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report
5. Respiratory Comorbidities Associated with Bronchiectasis in Patients with Common Variable Immunodeficiency in the USIDNET Registry
6. Inflammatory Proteomic Analysis of 22q11.2 Deletion Syndrome
7. Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development
8. A Registry Study of 240 Patients with X-Linked Agammaglobulinemia Living in the USA
9. Urine biomarker score captures response to induction therapy with lupus nephritis
10. Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 Duplications
11. Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development
12. Impact of medications on salivary flow rate in patients with xerostomia: a retrospective study by the Xeromeds Consortium
13. SGPL1 Deficiency: Nephrotic Syndrome with Lymphopenia
14. The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity
15. Risk Factors of Pneumonia in Primary Antibody Deficiency Patients Receiving Immunoglobulin Therapy: Data from the US Immunodeficiency Network (USIDNET)
16. Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee
17. X-Linked Agammaglobulinemia: Infection Frequency and Infection-Related Mortality in the USIDNET Registry
18. Implicating effector genes at COVID-19 GWAS loci using promoter-focused Capture-C in disease-relevant immune cell types
19. Single-cell analysis reveals heterogeneity of juvenile idiopathic arthritis fibroblast-like synoviocytes with implications for disease subtype
20. 22q11.2 Deletion and Duplication Syndromes and COVID-19
21. Chromatin Modifications in 22q11.2 Deletion Syndrome
22. Diagnostic Challenges in Pediatric Hemophagocytic Lymphohistiocytosis
23. The variable impact of the overdose crisis on organ donation among five Canadian provinces: a retrospective study
24. Infectious Complications Predict Premature CD8+ T-cell Senescence in CD40 Ligand-Deficient Patients
25. Self-Limited COVID-19 in a Patient with Artemis Hypomorphic SCID
26. The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee
27. Infection Phenotypes Among Patients with Primary Antibody Deficiency Mined from a US Patient Registry
28. PROMIS-29 survey confirms major impact of fatigue on health-related quality of life in common variable immunodeficiency
29. Adenosine Deaminase (ADA)–Deficient Severe Combined Immune Deficiency (SCID) in the US Immunodeficiency Network (USIDNet) Registry
30. The culture microenvironment of juvenile idiopathic arthritis synovial fibroblasts is favorable for endochondral bone formation through BMP4 and repressed by chondrocytes
31. Proteomic profiling of MIS-C patients indicates heterogeneity relating to interferon gamma dysregulation and vascular endothelial dysfunction
32. European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management
33. Lymphoproliferative Disease in CVID: a Report of Types and Frequencies from a US Patient Registry
34. Prophylactic Antibiotics Versus Immunoglobulin Replacement in Specific Antibody Deficiency
35. Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification
36. Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
37. The Association of Fetal Thymus Size with Subsequent T Cell Counts in 22q11.2 Deletion Syndrome
38. Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders
39. Outcomes for Nitazoxanide Treatment in a Case Series of Patients with Primary Immunodeficiencies and Rubella Virus-Associated Granuloma
40. Juvenile idiopathic arthritis fibroblast-like synoviocytes influence chondrocytes to alter BMP antagonist expression demonstrating an interaction between the two prominent cell types involved in endochondral bone formation
41. Prevalence of Granulomas in Patients With Primary Immunodeficiency Disorders, United States: Data From National Health Care Claims and the US Immunodeficiency Network Registry
42. Low Rates of Poliovirus Antibodies in Primary Immunodeficiency Patients on Regular Intravenous Immunoglobulin Treatment
43. Low Serum IgE Is a Sensitive and Specific Marker for Common Variable Immunodeficiency (CVID)
44. Complications Associated with Underweight Primary Immunodeficiency Patients: Prevalence and Associations Within the USIDNET Registry
45. The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies
46. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity
47. Nitazoxanide May Modify the Course of Progressive Multifocal Leukoencephalopathy
48. Autoimmune Cytopenias and Associated Conditions in CVID: a Report From the USIDNET Registry
49. Emerging Infections and Pertinent Infections Related to Travel for Patients with Primary Immunodeficiencies
50. Inflammatory Bowel Disease in Primary Immunodeficiencies
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