187 results on '"Renner, Ellen D."'
Search Results
2. Inborn Error of Immunity or Atopic Dermatitis: When to be Concerned and How to Investigate
3. A patient empowerment program for primary immunodeficiency improves quality of life in children and adolescents.
4. Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency
5. Reduced Immunoglobulin (Ig) G Response to Staphylococcus aureus in STAT3 Hyper-IgE Syndrome
6. Retained primary teeth in STAT3 hyper-IgE syndrome: early intervention in childhood is essential
7. Atopic dermatitis: Correlation of distinct risk factors with age of onset in adulthood compared to childhood
8. Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
9. Atopic dermatitis: factors associated with age of onset in adulthood versus childhood [Abstract]
10. Atopic dermatitis: correlation of distinct risk factors with age of onset in adulthood compared to childhood
11. Atopic dermatitis: Correlation of distinct risk factors with age of onset in adulthood compared to childhood
12. Targeted next-generation sequencing: A novel diagnostic tool for primary immunodeficiencies
13. Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation
14. Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency
15. Lung function improvement and airways inflammation reduction in asthmatic children after a rehabilitation program at moderate altitude
16. IL‐13, periostin and dipeptidyl‐peptidase‐4 reveal endotype‐phenotype associations in atopic dermatitis.
17. DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
18. Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children
19. Diagnostic approach to the hyper-IgE syndromes: Immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis
20. Class Switch Recombination Defects: impact on B cell maturation and antibody responses
21. Comèl-Netherton syndrome defined as primary immunodeficiency
22. A Novel Gain-of-Function IKBA Mutation Underlies Ectodermal Dysplasia with Immunodeficiency and Polyendocrinopathy
23. Lung Parenchyma Surgery in Autosomal Dominant Hyper-IgE Syndrome
24. Commensal bacteria-derived signals regulate basophil hematopoiesis and allergic inflammation
25. Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced TH17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome
26. Beneficial IFN-α treatment of tumorous herpes simplex blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency
27. Electrical impedance spectroscopy for the characterization of skin barrier in atopic dermatitis
28. Rescue of STAT3 Function in Hyper-IgE Syndrome Using Adenine Base Editing
29. Rituximab-induced long-term remission in two children with SLE
30. Additional file 2 of Retained primary teeth in STAT3 hyper-IgE syndrome: early intervention in childhood is essential
31. Additional file 3 of Retained primary teeth in STAT3 hyper-IgE syndrome: early intervention in childhood is essential
32. Additional file 1 of Retained primary teeth in STAT3 hyper-IgE syndrome: early intervention in childhood is essential
33. Challenges of genetic counseling in patients with autosomal dominant diseases, such as the hyper-IgE syndrome (STAT3-HIES)
34. Retained primary teeth in STAT3 hyper-IgE syndrome: early intervention in childhood is essential
35. STAT3 Mutation in the Original Patient with Job's Syndrome
36. Molecular Analysis of the MVK and TNFRSF1A Genes in Patients With a Clinical Presentation Typical of the Hyperimmunoglobulinemia D With Periodic Fever Syndrome: A Low-Penetrance TNFRSF1A Variant in a Heterozygous MVK Carrier Possibly Influences the Phenotype of Hyperimmunoglobulinemia D With Periodic Fever Syndrome or Vice Versa
37. STAT1 Gain-of-Function and Dominant Negative STAT3 Mutations Impair IL-17 and IL-22 Immunity Associated with CMC
38. Heterozygous signal transducer and activator of transcription 3 mutations in hyper-IgE syndrome result in altered B-cell maturation
39. Impact of high‐altitude therapy on type‐2 immune responses in asthma patients
40. Impaired memory B‐cell development and antibody maturation with a skewing toward IgE in patients with STAT3 hyper‐IgE syndrome
41. Retained primary teeth in STAT3 hyper-IgE syndrome: Early intervention in childhood is essential
42. Lung disease inSTAT3 hyper‐IgE syndrome requires intense therapy
43. Somatic alterations compromised molecular diagnosis of DOCK8 hyper-IgE syndrome caused by a novel intronic splice site mutation
44. Impact of high‐altitude therapy on type‐2 immune responses in asthma patients.
45. Perception of climate change in patients with chronic lung disease
46. Lung disease in STAT3 hyper‐IgE syndrome requires intense therapy.
47. Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
48. Outcome of HSCT in Adolescents and Young Adults with Non-SCID Primary Immunodeficiencies
49. DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
50. Targeted next-generation sequencing: a novel diagnostic tool for primary immunodeficiencies
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