Výsledky vyhledávání - "cardiovascular malformation"

Akademický článek

Exploring the Role of Modified Vascular Anatomical Molding (MVAM) in Prenatal Diagnosis Teaching and Prognosis Prediction of Fetal Complex Congenital Heart Disease (CCHD): A Preliminary Study

Autor: An P, Song L, Song P, Zhang J, Lin Y, Feng G, Liu J

Publikováno v: International Journal of General Medicine, Vol Volume 16, Pp 3229-3245 (2023)

Peng An,1,2,* Lina Song,1,* Ping Song,3,* Junyan Zhang,1,3 Yong Lin,1,3 Guoyan Feng,1 Junjie Liu3 1Department of Radiology, Xiangyang No.1 People’s Hospital, Hubei University of Medicine, Xiangyang, 441000, People’s Republic of China;

Externí odkaz: https://doaj.org/article/07ee204da26b452f8ddaa98ead67940d

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Akademický článek

Neonatal diagnosis of isolated absence of the right pulmonary artery: a case report and review of the literature

Autor: Akamin Raymond, Ettore Pedretti, Giuseppina Privitera, Cristina Cicero, Giacomo Biasucci

Publikováno v: Italian Journal of Pediatrics, Vol 44, Iss 1, Pp 1-4 (2018)

Abstract Background Unilateral absence of the pulmonary artery (UAPA) is a rare congenital malformation often associated with other cardiac anomalies; however it may occur as an isolated lesion. Isolated absence of the right pulmonary artery is twice

Externí odkaz: https://doaj.org/article/c3e8098b5b8f416a99a34216d7bb2317

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Akademický článek

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Akademický článek

Preliminary Evidence for Aortopathy and an X-Linked Parent-of-Origin Effect on Aortic Valve Malformation in a Mouse Model of Turner Syndrome

Autor: Robert B. Hinton, Amy M. Opoka, Obah A. Ojarikre, Lawrence S. Wilkinson, William Davies

Publikováno v: Journal of Cardiovascular Development and Disease, Vol 2, Iss 3, Pp 190-199 (2015)

Turner syndrome (TS), most frequently caused by X-monosomy (45,X), is characterized in part by cardiovascular abnormalities, including aortopathy and bicuspid aortic valve (BAV). There is a need for animal models that recapitulate the cardiovascular

Externí odkaz: https://doaj.org/article/0764d810f382416aac9b5dcc306a034c

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Akademický článek

Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach

Autor: Robert B. Hinton, Kim L. McBride, Steven B. Bleyl, Neil E. Bowles, William L. Border, Vidu Garg, Teresa A. Smolarek, Seema R. Lalani, Stephanie M. Ware

Publikováno v: Journal of Cardiovascular Development and Disease, Vol 2, Iss 2, Pp 76-92 (2015)

Cardiovascular malformations (CVMs) are the most common birth defect, occurring in 1%–5% of all live births. Although the genetic contribution to CVMs is well recognized, the genetic causes of human CVMs are identified infrequently. In addition, a

Externí odkaz: https://doaj.org/article/61b454d754e540f9ab448512c708dd17

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Akademický článek

Risk factors predisposing to congenital heart defects

Autor: Faheem Ul Haq, Fatima Jalil, Saman Hashmi, Maliha Iqbal Jumani, Aamer Imdad, Mehnaz Jabeen, Javad Tauseef Hashmi, Furqan Bin Irfan, Muhammad Imran, Mehnaz Atiq

Publikováno v: Annals of Pediatric Cardiology, Vol 4, Iss 2, Pp 117-121 (2011)

Introduction: Congenital heart disease (CHD) is associated with multiple risk factors, consanguinity may be one such significant factor. The role of consanguinity in the etiology of CHD is supported by inbreeding studies, which demonstrate an autosom

Externí odkaz: https://doaj.org/article/8b647babc5954b388e66d889201b3ab6

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