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Pulmonary interstitial glycogenosis

 
National Institutes of Health

Papers overview

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Review
2018
Review
2018
BACKGROUND Pulmonary interstitial glycogenosis (PIG) is a rare paediatric interstitial lung disease of unknown cause. The… Expand
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2017
2017
Primary or isolated pulmonary interstitial glycogenosis (PIG) is a rare disease presenting as tachypnea and hypoxemia during the… Expand
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2014
2014
Pulmonary interstitial glycogenosis (PIG) is an idiopathic interstitial lung disease of infants. The underlying pulmonary… Expand
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2014
2014
We describe an infant prenatally diagnosed with hydrops fetalis ultimately found to have Noonan syndrome (NS). Prior to genetic… Expand
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2012
2012
A neonate with pulmonary interstitial glycogenosis, pulmonary hypertension, and hypertrophic cardiomyopathy is described. The… Expand
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2012
2012
BackgroundPulmonary interstitial glycogenosis (PIG) arises from a developmental disorder of the pulmonary mesenchyme and presents… Expand
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2011
2011
In 2004, we reported on a neonate with pulmonary interstitial glycogenosis (PIG), with favorable outcome at the age of 19 months… Expand
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2010
2010
Pulmonary interstitial glycogenosis (PIG) is a rare pediatric interstitial lung disease. We report a case of a term boy… Expand
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2009
2009
Pulmonary interstitial glycogenosis (PIG) is an enigmatic lung disorder of unknown etiology that presents with neonatal… Expand
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2008
2008
We present a 5-year-old boy who initially presented during infancy with pulmonary interstitial glycogenosis (PIG) and recurrent… Expand
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