225: ORTNER SYNDROME AS SYMPTOM OF HEREDITARY HEMORRHAGIC TELANGIECTASIA WITH PULMONARY HYPERTENSION. (January 2018)

Record Type:: Journal Article
Title:: 225: ORTNER SYNDROME AS SYMPTOM OF HEREDITARY HEMORRHAGIC TELANGIECTASIA WITH PULMONARY HYPERTENSION. (January 2018)
Main Title:: 225
Authors:: Alsheikh, Batool
Wigby, Kristen
Carroll, Jeanne
Nahas, Shareef
Chowdhury, Shimul
Dimmock, David
Murthy, Raghav
Yeh, Justin
Harvey, Helen
Coufal, Nicole
Abstract:
Is Part Of:: Critical care medicine. Volume 46:Supplement 1 1(2018)
Journal:: Critical care medicine
Issue:: Volume 46:Supplement 1 1(2018)
Issue Display:: Volume 46, Issue 1 (2018)
Year:: 2018
Volume:: 46
Issue:: 1
Issue Sort Value:: 2018-0046-0001-0000
Page Start:
Page End:
Publication Date:: 2018-01
Subjects:: Critical care medicine -- Periodicals
Soins intensifs -- Périodiques
616.028
Journal URLs:: http://journals.lww.com/ccmjournal/Pages/default.aspx ↗
http://journals.lww.com ↗
DOI:: 10.1097/01.ccm.0000528244.78304.54 ↗
Languages:: English
ISSNs:: 0090-3493
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3487.451000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 6100.xml