Allergic Bronchopulmonary Aspergillosis
What's New
Last Posted: Jul 26, 2023
- Heterozygous CARD9 mutation favors the development of allergic bronchopulmonary aspergillosis.
Xia Xu, et al. Chinese medical journal 2023 0 - Mutations in EEA1 are associated with allergic bronchopulmonary aspergillosis and affect phagocytosis of Aspergillus fumigatus by human macrophages.
Overton Nicola L D, et al. PloS one 2018 0 (3) e0185706 - Resistin is elevated in cystic fibrosis sputum and correlates negatively with lung function.
Forrest Osric A, et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2018 0 (1) 64-70 - Risk factors and impact of allergic bronchopulmonary aspergillosis in Pseudomonas aeruginosa-negative CF patients.
De Baets Frans, et al. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2018 0 (7) 726-731 - Risk factors for lung disease progression in children with cystic fibrosis.
van Horck Marieke, et al. The European respiratory journal 2018 0 (6) - Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosis.
Liu Keqiang, et al. Orphanet journal of rare diseases 2020 0 (1) 150 - Assessing the health risk of living near composting facilities on lung health, fungal and bacterial disease in cystic fibrosis: a UK CF Registry study.
Khan Muhammad Saleem, et al. Environmental health : a global access science source 2022 0 (1) 130 - Occurrence of Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations in Patients with Allergic Bronchopulmonary Aspergillosis Complicating Asthma.
Kanaujia Rimjhim, et al. Mycopathologia 2022 0 (2-3) 147-155 - The Role of HLA-DRB1 Alleles in Pulmonary Cystic Fibrosis.
Asef Alireza, et al. Iranian journal of allergy, asthma, and immunology 2022 0 (2) 189-196 - Association of Serum TGF-?1 Levels with Different Clinical Phenotypes of Cystic Fibrosis Exacerbation.
Sagwal Swati, et al. Lung 2020 0 (2) 377-383
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:May 01, 2024
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