267 results on '"Lawrence, Monica G."'
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2. Impaired Response to Polysaccharide Vaccine in Selective IgE Deficiency
3. Disparities in Diagnosis, Access to Specialist Care, and Treatment for Inborn Errors of Immunity
4. PLCG2-associated immune dysregulation (PLAID) comprises broad and distinct clinical presentations related to functional classes of genetic variants
5. Further evidence of a type 2 inflammatory signature in chronic obstructive pulmonary disease or emphysema
6. Use of Vaccines in Patients Receiving Dupilumab, A Systematic Review and Expert Delphi Consensus Recommendation: A position paper of the American College of Allergy, Asthma and Immunology
7. Natural history of infants with non-SCID T cell lymphopenia identified on newborn screen
8. Specific antibody deficiency: pearls and pitfalls for diagnosis
9. Lower viral loads in subjects with rhinovirus-challenged allergy despite reduced innate immunity
10. Interleukin-5 receptor alpha (CD125) expression on human blood and lung neutrophils
11. IgE deficiency is not associated with hypogammaglobulinemia in a large cohort of military recruits
12. A Toolkit and Framework for Optimal Laboratory Evaluation of Individuals with Suspected Primary Immunodeficiency
13. Novel Treatment-Refractory Preschool Wheeze Phenotypes Identified by Cluster Analysis of Lung Lavage Constituents
14. Yao syndrome in a child with C2 deficiency
15. Rash and Diarrhea
16. Shortness of Breath
17. Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & Immunology
18. Persistent Unexplained Transaminitis in COPA Syndrome
19. Lung Lavage Granulocyte Patterns and Clinical Phenotypes in Children with Severe, Therapy-Resistant Asthma
20. Disparities in Diagnosis, Access to Specialist Care and Treatment for Inborn Errors of Immunity
21. Novel Pathogenic C2 Variant Associated with Disseminated GBS Infection
22. 2019 Clinical Immunology Society Compensation Survey
23. Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism
24. Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation–polyendocrinopathy–enteropathy–X-linked–like syndrome
25. Half-life of IgE in serum and skin: Consequences for anti-IgE therapy in patients with allergic disease
26. Use of Genetic Testing for Primary Immunodeficiency Patients
27. Low Serum IgE Is a Sensitive and Specific Marker for Common Variable Immunodeficiency (CVID)
28. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome
29. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome
30. Basic science for the clinician: Mechanisms of sublingual and subcutaneous immunotherapy
31. 6-Year-Old Boy with Recurrent Sinopulmonary Infections and Lymphadenopathy
32. Gastrointestinal Manifestations of STAT3-Deficient Hyper-IgE Syndrome
33. Over-expression of CRTH2 indicates eosinophilic inflammation and poor prognosis in recurrent nasal polyps
34. Navigating diagnostic options for inborn errors of immunity in children: a case-based illustration
35. T-cell biology in immunotherapy
36. Pathogenic CD4+ T cells in patients with asthma
37. Tregs require WASP to restrain Th2-mediated food allergy
38. The continuum of Allergy-Immunology Fellowship Training and continuing certification embraces competency based medical education
39. Low IgG trough and lymphocyte subset counts are associated with hospitalization for COVID-19 in patients with primary antibody deficiency
40. Correction to: Use of Genetic Testing for Primary Immunodeficiency Patients
41. Loss of B Cells in Patients with Heterozygous Mutations in IKAROS
42. Patterns of Allergic Sensitization in High IgE Syndromes
43. Over-expression of CRTH2 indicates eosinophilic inflammation and poor prognosis in recurrent nasal polyps.
44. Racial, Ethnic, and Socioeconomic Disparities in the Diagnosis and Management of Primary Immunodeficiencies
45. GATA3 haploinsufficiency does not block allergic sensitization or atopic disease
46. Characteristic CD45RA / CD45RO maturation pattern by flow cytometry associated with the CD45 C77G polymorphism
47. Bronchoalveolar lavage cytokine patterns in children with severe neutrophilic and paucigranulocytic asthma
48. Gain-of-function STAT1 mutations are associated with PD-L1 overexpression and a defect in B-cell survival
49. Dominant Gain-of-Function Mutations in STAT1 and FOXP3+ IPEX-Like Disease
50. Lymphopenia is Associated with a TH2 Phenotype and Specific Allergen Sensitivity in Patients with ADA-SCID
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