|1.||Limper, Andrew H: 2 articles (09/2006 - 06/2005)|
|2.||Agarwal, Suneet: 1 article (12/2015)|
|3.||Cahan, Patrick: 1 article (12/2015)|
|4.||Moon, Diane H: 1 article (12/2015)|
|5.||Hofmann, Inga: 1 article (12/2015)|
|6.||Tai, Albert K: 1 article (12/2015)|
|7.||Boyraz, Baris: 1 article (12/2015)|
|8.||Segal, Matthew: 1 article (12/2015)|
|9.||Guinan, Eva: 1 article (12/2015)|
|10.||Schwartz, David A: 1 article (01/2013)|
|1.||Pulmonary Fibrosis (Hamman Rich Syndrome)
03/29/2007 - "To test the hypothesis that familial idiopathic pulmonary fibrosis may be caused by short telomeres, we screened 73 probands from the Vanderbilt Familial Pulmonary Fibrosis Registry for mutations in hTERT and hTR. "
01/01/1983 - "[Current concepts on the etiology and pathogenesis of idiopathic fibrosing alveolitis (Hamman-Rich disease)]."
07/01/1980 - "[X-ray diagnosis of the respiratory organ lesion in diffuse fibrosing alveolitis (Hamman-Rich disease)]."
01/01/1971 - "[2 cases of progressive interstitial pulmonary fibrosis (Hamman-Rich disease)]."
11/01/1959 - "Familial fibrocystic pulmonary dysplasia and its relation to Hamman-Rich syndrome."
|2.||Idiopathic Pulmonary Fibrosis
01/01/2013 - "We previously identified a MUC5B gene promoter-variant that is a risk allele for sporadic and familial Idiopathic Pulmonary Fibrosis/Usual Interstitial Pneumonia (IPF/UIP). "
09/01/2006 - "The pathogenesis of both idiopathic pulmonary fibrosis and familial idiopathic pulmonary fibrosis remains unclear. "
09/01/2006 - "The clinical characteristics of familial idiopathic pulmonary fibrosis are indistinguishable from sporadic idiopathic pulmonary fibrosis. "
06/01/2005 - "Familial idiopathic pulmonary fibrosis (FIPF) has been defined as idiopathic pulmonary fibrosis (IPF) occurring in two or more members of a family. "
|3.||Interstitial Lung Diseases (Interstitial Lung Disease)
01/01/2010 - "Diffuse alveolar damage [DAD] from unknown causes is termed acute interstitial pneumonia [AIP], and is synonymous with cases of Hamman-Rich disease. "
09/01/2004 - "It focuses on the inherited mendelian diseases in which pulmonary fibrosis is part of the clinical phenotype and the genetics of familial idiopathic pulmonary fibrosis and other rare inherited interstitial lung diseases. "
|4.||Dyskeratosis Congenita (X-Linked Dyskeratosis Congenita)
|5.||Autoimmune Polyendocrinopathies (Schmidt Syndrome)