References
- Kurland G, Deterding RR, Hagood JS, et al. An official american thoracic society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy. Am J Respir Crit Care Med 2013;188:376-94
- Deutsch GH, Young LR, Deterding RR, et al. Diffuse lung disease in young children: application of a novel classification scheme. Am J Respir Crit Care Med 2007;176:1120-8
- Deterding RR, Pye C, Fan LL, Langston C. Persistent tachypnea of infancy is associated with neuroendocrine cell hyperplasia. Pediatr pulmonol 2005;40:157-65
- Nogee LM. Genetic basis of children’s interstitial lung disease. Pediatr Allergy Immunol Pulmonol 2010;23:15-24
- Stankiewicz P, Sen P, Bhatt SS, et al. Genomic and genic deletions of the fox gene cluster on 16q24.1 and inactivating mutations of foxf1 cause alveolar capillary dysplasia and other malformations. Am J Hum Genet 2009;84:780-91
- Langston C, Patterson K, Dishop MK, et al. A protocol for the handling of tissue obtained by operative lung biopsy: recommendations of the child pathology co-operative group. Pediatr Dev Pathol 2006;9:173-80
- Hamvas A, Deterding RR, Wert SE, et al. Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene nkx2-1. Chest 2013;144:794-804
- Sen P, Yang Y, Navarro C, et al. Novel foxf1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain. Hum mutat 2013;34:801-11
- Bush A, Anthony G, Barbato A, et al. Research in progress003A put the orphanage out of business. Thorax 2013;68:971-3