A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancy.
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Interstitial lung disease in childrenThe molecular era of surfactant biology."A remarkable experience of god, shaping us as a family": parents' use of faith following child's rare disease diagnosis.Childhood interstitial lung disease: A systematic review.Children's Interstitial and Diffuse Lung Disease. Progress and Future Horizons.Update on Diffuse Lung Disease in Children.Interstitial lung disease in newborns.Neuroendocrine cell hyperplasia of infancy: an unusual cause of hypoxemia in children.Persistent Lung Disease in Adults with NKX2.1 Mutation and Familial Neuroendocrine Cell Hyperplasia of Infancy.Interstitial lung disease of infancy caused by a new NKX2-1 mutation.Rare Becomes More Common: Recognizing Neuroendocrine Cell Hyperplasia of Infancy in Everyday Pulmonary Consultations.Role of High-Resolution Chest Computed Tomography in a Child with Persistent Tachypnoea and Intercostal Retractions: A Case Report of Neuroendocrine Cell Hyperplasia.Pulmonary Neuroendocrine Cell Hyperplasia Associated with Surfactant Protein C Gene Mutation.Molecular alterations of neuroendocrine tumours of the lung.FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?Bombesin staining in neuroendocrine cell hyperplasia of infancy (NEHI) and other childhood interstitial lung diseases (chILD).
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P2860
A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancy.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on October 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
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A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
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A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
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A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
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A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
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A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
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A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
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Alan S Brody
Gail H Deutsch
Lawrence M Nogee
Lisa R Young
Ronald E Bokulic
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P304
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10.1378/CHEST.13-0811
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P577
2013-10-01T00:00:00Z