Results 101 to 110 of about 17,996 (223)

Coronary-to-pulmonary artery fistula in a patient with atypical chest pain: case presentation and literature review. [PDF]

Surg Radiol Anat
Rusali AC, Lupu CI, Manolache MM, Rusali LM, Bordei P, Cojocaru L.   +5 more
europepmc   +1 more source

Chapter 4: Normal and Anomalous Coronary Arteries in Humans. Part 1: Historical Background [PDF]

, 1999
Angelini, Paolo, Chan, Jr., Albert V., Diez, Jose\u27 G., Villason, Salvado   +3 more
core   +1 more source

Anomalous Coronary Arteries: Anatomic and Functional Assessment by Coronary and Perfusion Cardiovascular Magnetic Resonance in Three Sisters [PDF]

Combined coronary and perfusion cardiovascular magnetic resonance was performed in three sisters with angina and suspected anomalous coronary arteries.
Christine H. Lorenz, Dudley J. Pennell, Nicholas H. Bunce, Peter D. Gatehouse, Shelley L. Rahman   +4 more
core  

Decoding Hidden Pathways: A Comprehensive Exploration of Anomalous Coronary Arteries. [PDF]

Cureus
Vallurupalli A, Thachathodiyl R.
europepmc   +1 more source

Improving performance of coronary artery segmentation using calculated vessel location from the angiogram

, 2018
M. Tenekeci, H. Pehlivan, Y. Kaya
semanticscholar   +1 more source

Evaluation of Coronary Artery Disease and Coronary Anomalies with a Handheld Smartphone

Journal of digital imaging, 2017
C. Lin, Stefan L. Zimmerman, L. Chu, J. Eng, E. Fishman   +4 more
semanticscholar   +1 more source

Rare congenital coronary artery anomalies diagnosed by coronary CT angiography: A 4-case series. [PDF]

Radiol Case Rep
Lam LV, Thuong TM, Thang TQ, Huong VTT, Vu TM, Ha HPT, Linh DDT, Thinh PX.   +7 more
europepmc   +1 more source

CADASIL or <i>NOTCH3</i> mutaion spectrum diseases? Interpretation of <i>NOTCH3</i> mutations and clinical heterogeneity in CADASIL. [PDF]

Front Neurol
Wang Y, Liu Y, Mo H, Han Y, Jing Y, Deng F.   +5 more
europepmc   +1 more source

Multimodality imaging-guided transcatheter closure of a tortuous LCX-CS fistula: a case report. [PDF]

Eur Heart J Case Rep
Sekii R, Kato S, Fukui K, Utsunomiya D, Hibi K.   +4 more
europepmc   +1 more source

MYRF gene mutation leading to coronary artery anomaly combined with 46,XY sex development disorder, a case report and literature review. [PDF]

BMC Pediatr
Ding J, Lv Z, Zhen Z, Gai Y, Xiao Y.
europepmc   +1 more source