Results 91 to 100 of about 11,531 (208)

Brief review of right aortic arch with aberrant left subclavian artery [PDF]

, 2019
Development anomalies of the aortic arch and its major branches are rare congenitalcardiovascular disorders.
Öztaş, Didem Melis, Conkbayır, Cenk, Umutlu, Muzaffer, Erdinç, İbrahim, Uğurlucan, Murat, Ulukan, Mustafa Özer, Alpagut, Ufuk, Badem, Serdar, Ertan, Melike, Ünal, Orçun, Beyaz, Metin Onur   +10 more
core   +1 more source

Data_Sheet_1_Surgical treatment strategies for patients with type A aortic dissection involving arch anomalies.PDF

, 2022
ObjectiveThe aim of the study was to investigate surgical modalities and outcomes in patients with type A aortic dissection involving arch anomalies.MethodPatients with type A aortic dissection who underwent surgical treatment at our center between ...
Xin Li (51274), Yaorong Liu (10887579), Jie Liu (15128), Tucheng Sun (10887582), Donglin Zhuang (12227924), Zhichao Liang (2310493), Zhen Zhang (86004), Yongchao Yang (546178), Jinlin Wu (116930), ZeRui Chen (13776736), Jiade Zhu (6418286), Ruixin Fan (9664632), Jue Yang (290952), Guang Tong (386966), Changjiang Yu (319189)   +14 more
core   +1 more source

Congenital Anomalies of Aortic Arch: CT Angiography

, 2001
Aortic arch anomalies result from the failure of an embryonic vascular structure to persist and regress in the usual manner during formation of the aortic arch.
김태훈
core  

Utility of prenatal ultrasound in diagnosis and prognosis of aortic arch obstruction: a 10-year single-center retrospective study

Frontiers in Medicine
ObjectiveThis study aimed to evaluate the prenatal echocardiographic features, diagnostic accuracy, associated anomalies, and early postnatal outcomes of fetal aortic arch obstruction, with particular emphasis on differentiating interrupted aortic arch ...
He Li, Jinwen Chen, Wen Ling, Qiumei Wu, Biying Huang, Guorong Lyu, Caihong Jiang, Zongjie Weng   +7 more
doaj   +1 more source

Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-CardioFacial syndrome) [PDF]

, 2005
Deletion 22q11.2 syndrome (Del22) (DiGeorge/Velo-Cardio-Facial syndrome) is characterized by congenital heart defect (CHD), palatal anomalies, facial dysmorphisms, neonatal hypocalcemia, immune deficit, speech and learning disabilities. CHD is present
Marino, Bonnie, Capolino, Rossella, Digilio, Maria Cristina, Dallapiccola, B.   +3 more
core  

Retrospective analytical five months study of aortic arch abnormalities

, 2016
Background: Aortic arch abnormalities include congenital anomalies and acquired pathologies. Many of aortic arch congenital anomalies are asymptomatic lesions. But some of these anomalies are symptomatic and need to be treated.
Chelliah, Nellaiappan
core   +1 more source

When Arteria lusoria meets Truncus bicaroticus: one of the rarest combinations of aortic arch anomalies. [PDF]

Radiol Case Rep, 2022
Marsafi O, Chahbi Z, Wakrim S.
europepmc   +1 more source

Aortic arch anomalies: are they contra-indications for CAS?

, 2008
In the chapter is reported the role of the aortic arch anomalies in the outcome of carotid ...
M. Gargiulo, STELLA, ANDREA, GARGIULO, MAURO, M. Ferri, FERRI, MONICA, FREYRIE, Antonio, F. Fretasi, GL Faggioli, FAGGIOLI, GIANLUCA   +8 more
core  

3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation. [PDF]

J Cardiovasc Magn Reson, 2022
Uus AU, van Poppel MPM, Steinweg JK, Grigorescu I, Ramirez Gilliland P, Roberts TA, Egloff Collado A, Rutherford MA, Hajnal JV, Lloyd DFA, Pushparajah K, Deprez M.   +11 more
europepmc   +1 more source

Symptomatic Double Aortic Arch Anomaly [PDF]

Clinical Gastroenterology and Hepatology, 2021
Dhairya A. Lakhani, Fletcher Moore, Eyassu Hailemichael   +2 more
openaire   +2 more sources