295 results on '"Deutsch, Gail H."'
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2. Congenital and Developmental Causes of Cystic Lung Disease
3. Mast cell surfaceome characterization reveals CD98 heavy chain is critical for optimal cell function
4. Islet Interleukin-1β Immunoreactivity Is an Early Feature of Cystic Fibrosis That May Contribute to β-Cell Failure
5. Bulk RNA sequencing of human pediatric lung cell populations reveals unique transcriptomic signature associated with postnatal pulmonary development
6. The US national registry for childhood interstitial and diffuse lung disease: Report of study design and initial enrollment cohort.
7. Lung biopsy in the diagnosis and management of chILD.
8. Pediatric Cystic Lung Lesions: Where Are We Now?
9. The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children
10. Congenital and Developmental Causes of Cystic Lung Disease
11. 5 - Acquired and Idiopathic Disorders in Neonates and Young Children
12. A novel non‐recurrent CNV deletion involving TBX4 and leaving TBX2 intact causes congenital alveolar dysplasia
13. New insights into the natural history of bronchopulmonary dysplasia from proteomics and multiplexed immunohistochemistry
14. Pathology of the Lung Through Childhood
15. List of Contributors
16. Histologic Phenotypes of Bronchopulmonary Dysplasia and Childhood Interstitial and Diffuse Lung Disease
17. Proteome analysis of mast cell releasates reveals a role for chymase in the regulation of coagulation factor XIIIA levels via proteolytic degradation
18. A novel non‐recurrent CNV deletion involving TBX4 and leaving TBX2 intact causes congenital alveolar dysplasia.
19. 47 - Childhood Interstitial Lung Disease More Prevalent in Infancy
20. Childhood Interstitial Lung Disease Disorders More Prevalent in Infancy
21. Contributors
22. Lung biopsy in the diagnosis and management of chILD
23. Dedicator of cytokinesis 8 (DOCK8) is a negative regulator of skin mast cell function
24. Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia and Neuroendocrine Hyperplasia of Infancy
25. Epithelial-Derived Inflammation Disrupts Elastin Assembly and Alters Saccular Stage Lung Development
26. Pulmonary fibrosis may begin in infancy: from childhood to adult interstitial lung disease
27. Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis
28. FGF18 promotes human lung branching morphogenesis through regulating mesenchymal progenitor cells
29. Idiopathic and Familial Pulmonary Arterial Hypertension
30. Contributors
31. A Mutation in TTF1/NKX2.1 Is Associated With Familial Neuroendocrine Cell Hyperplasia of Infancy
32. Serum proteome analysis of systemic JIA and related lung disease identifies distinct inflammatory programs and biomarkers
33. Tyrosine kinase‐altered spindle cell neoplasms with EGFR internal tandem duplications
34. Identification of Distinct Inflammatory Programs and Biomarkers in Systemic Juvenile Idiopathic Arthritis and Related Lung Disease by Serum Proteome Analysis
35. Neonatal Hyperoxia Activates Activating Transcription Factor 4 to Stimulate Folate Metabolism and Alveolar Epithelial Type 2 Cell Proliferation
36. Neuroendocrine Cell Distribution and Frequency Distinguish Neuroendocrine Cell Hyperplasia of Infancy From Other Pulmonary Disorders
37. Proteomic Analysis of Human Lung Development
38. Imaging Review of Obstetric Sequelae of Maternal Diabetes Mellitus
39. Lipofibroblast Phenotype in Pulmonary Interstitial Glycogenosis
40. List of Contributors
41. Multimodality Imaging Evaluation of Fetal Spine Anomalies with Postnatal Correlation
42. Lung disease manifestations in Down syndrome
43. Diffuse Lung Disease in Biopsied Children 2 to 18 Years of Age. Application of the chILD Classification Scheme
44. Interstitial Lung Disease in Children with Rubinstein‐Taybi Syndrome
45. Pulmonary interstitial glycogenosis: words of caution
46. Chapter 2 - Histologic Phenotypes of Bronchopulmonary Dysplasia and Childhood Interstitial and Diffuse Lung Disease
47. A Kindred of Children With Interstitial Lung Disease
48. Perinatal increases in TGF-[alpha] disrupt the saccular phase of lung morphogenesis and cause remodeling: microarray analysis
49. Molecular Insights into Congenital Disorders of the Digestive System
50. Childhood Interstitial Lung Disease Disorders More Prevalent in Infancy
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