scholarly journals Hepatopulmonary syndrome : a rare diagnosis or easily missed entity?

QJM ◽  
2014 ◽  
Vol 107 (7) ◽  
pp. 565-566 ◽  
Author(s):  
R. Shah ◽  
O. Mousa ◽  
S. John
JAMA ◽  
1966 ◽  
Vol 197 (5) ◽  
pp. 31-31 ◽  
Author(s):  
A. F. North
Keyword(s):  

2020 ◽  
Vol 158 (6) ◽  
pp. S-1460-S-1461
Author(s):  
Shoma Bommena ◽  
Nael Haddad ◽  
Sumit Agarwal ◽  
Sarabdeep Mann ◽  
Layth AL-Jashaami ◽  
...  

2009 ◽  
Vol 47 (05) ◽  
Author(s):  
V Fuhrmann ◽  
A Drolz ◽  
N Kneidinger ◽  
R Kitzberger ◽  
J Warszawska ◽  
...  

2016 ◽  
Vol 64 (S 01) ◽  
Author(s):  
B. Mayr ◽  
S. Buchholz ◽  
M. Lühr ◽  
C. Hagl ◽  
M. Pichlmaier

2008 ◽  
Vol 39 (01) ◽  
Author(s):  
H Weigand-Brunnhölzl ◽  
A Enders ◽  
F Heinen
Keyword(s):  

2021 ◽  
Vol 24 ◽  
pp. 200507
Author(s):  
Savanah D. Gisriel ◽  
Kenneth W. Hung ◽  
Demetrios T. Braddock ◽  
Stuart Seropian ◽  
Francine M. Foss ◽  
...  

2020 ◽  
pp. 1-3
Author(s):  
Simona Boroni Grazioli ◽  
Marc-Philip Hitz ◽  
Inga Voges

Abstract A 17-year-old boy with a history of dyspnea attacks and chest pain was referred to our paediatric cardiology department. Electrocardiogram at presentation showed T-wave inversion in the inferior leads. Cardiovascular magnetic resonance imaging revealed the rare diagnosis of apical hypertrophic cardiomyopathy with subendocardial late gadolinium enhancement, missed by echocardiography.


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