A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancy.

A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancy.

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http://www.wikidata.org/entity/Q37209566
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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A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancy.

Item
http://www.wikidata.org/entity/Q37209566
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
@en
A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
@nl
type
label
A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
@en
A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
@nl
prefLabel
A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
@en
A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P698
P932
P356
P1433
P1476
A mutation in TTF1/NKX2.1 is a ...... e cell hyperplasia of infancy.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P698
P932