- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Recurrent hemoptysis: An unusual cause and novel management ; volume:26 ; number:02 ; year:2016 ; pages:267-270
The Indian journal of radiology and imaging ; 26, Heft 02 (2016), 267-270
- Contributor
-
Surya, Praharsha
Keshava, Shyamkumar N.
Irodi, Aparna
Vyas, Sunil
Thangakunam, Balamugesh
- DOI
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10.4103/0971-3026.184412
- URN
-
urn:nbn:de:101:1-2021090210204354273485
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:35 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Surya, Praharsha
- Keshava, Shyamkumar N.
- Irodi, Aparna
- Vyas, Sunil
- Thangakunam, Balamugesh
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Mycobacterium tuberculosis aortic graft infection with recurrent hemoptysis: a case report
Recurrent catamenial hemoptysis: diagnostic challenges and management strategies—a case report
Hemoptysis and Endometriosis: An Unusual Association — Case Report and Review of the Literature
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A novel recurrent mutation in ATP1A3 causes CAPOS syndrome
An Unusual Cause of Cholangitis
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Isolated unilateral absence of pulmonary artery- an unusual cause of hemoptysis: a case report
An uncommon cause of hemoptysis: aortobronchial fistula
Hydatid cyst disease of the lung as an unusual cause of massive hemoptysis: a case report
A child with recurrent pallor and hemoptysis: Diagnostic challenges
Mycobacterium tuberculosis aortic graft infection with recurrent hemoptysis: a case report
Recurrent catamenial hemoptysis: diagnostic challenges and management strategies—a case report
Hemoptysis and Endometriosis: An Unusual Association — Case Report and Review of the Literature
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Hematemesis or hemoptysis? Pulmonary hydatidosis presenting with hemoptysis, case report
A novel recurrent mutation in ATP1A3 causes CAPOS syndrome
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