Iron deposition and increased alveolar septal capillary density in nonfibrotic lung tissue are associated with pulmonary hypertension in idiopathic pulmonary fibrosis

zu Verbundenen Objekten

Standort
Deutsche Nationalbibliothek Frankfurt am Main
ISSN
1465-993X
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
online resource.

Erschienen in
Iron deposition and increased alveolar septal capillary density in nonfibrotic lung tissue are associated with pulmonary hypertension in idiopathic pulmonary fibrosis ; volume:11 ; number:1 ; day:14 ; month:4 ; year:2010 ; pages:1-7 ; date:12.2010
Respiratory research ; 11, Heft 1 (14.4.2010), 1-7, 12.2010

Urheber
Kim, Kyung-Hee
Beteiligte Personen und Organisationen
Maldonado, Fabien
Ryu, Jay H.
Eiken, Patrick W.
Hartman, Thomas E.
Bartholmai, Brian J.
Decker, Paul A.
Yi, Eunhee S.
SpringerLink (Online service)

DOI
10.1186/1465-9921-11-37
URN
urn:nbn:de:1111-2016060311422
Rechteinformation
Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:49 MESZ

Datenpartner

Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Original beim Datenpartner anzeigen

Beteiligte

  • Kim, Kyung-Hee
  • Maldonado, Fabien
  • Ryu, Jay H.
  • Eiken, Patrick W.
  • Hartman, Thomas E.
  • Bartholmai, Brian J.
  • Decker, Paul A.
  • Yi, Eunhee S.
  • SpringerLink (Online service)

Ähnliche Objekte (12)

Impaired lipid metabolism in idiopathic pulmonary alveolar proteinosis

Impaired lipid metabolism in idiopathic pulmonary alveolar proteinosis

Pulmonary capillary pressure in pulmonary hypertension

Pulmonary capillary pressure in pulmonary hypertension

Clinical significance of serum lipids in idiopathic pulmonary alveolar proteinosis

Clinical significance of serum lipids in idiopathic pulmonary alveolar proteinosis

Pulmonary hypertension in idiopathic pulmonary fibrosis

Pulmonary hypertension in idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis

Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis

Multiomic analysis of monocyte-derived alveolar macrophages in idiopathic pulmonary fibrosis

Multiomic analysis of monocyte-derived alveolar macrophages in idiopathic pulmonary fibrosis

Genetic recording of transient endothelial activation in distinct alveolar capillary cells during pulmonary fibrosis

Genetic recording of transient endothelial activation in distinct alveolar capillary cells during pulmonary fibrosis

Decline in Mast Cell Density During Diffuse Alveolar Damage in Idiopathic Pulmonary Fibrosis

Decline in Mast Cell Density During Diffuse Alveolar Damage in Idiopathic Pulmonary Fibrosis

Correction to: Multiomic analysis of monocyte-derived alveolar macrophages in idiopathic pulmonary fibrosis

Correction to: Multiomic analysis of monocyte-derived alveolar macrophages in idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis: moving forward

Idiopathic pulmonary fibrosis: moving forward

Capillary pCO2 helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction

Capillary pCO2 helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction

Verbundene Objekte