Results 121 to 130 of about 58,639 (311)

Building an Intelligent Cardiovascular System Platform: Embedding Artificial Intelligence across All Facets of Cardiovascular Medicine

Advanced Intelligent Systems, EarlyView.
This paper presents an integrated AI‐driven cardiovascular platform unifying multimodal data, predictive analytics, and real‐time monitoring. It demonstrates how artificial intelligence—from deep learning to federated learning—enables early diagnosis, precision treatment, and personalized rehabilitation across the full disease lifecycle, promoting a ...
Mowei Kong, Xingwei Zhao, Qiuting Li, Yang Yu, Chunxiang Zhang   +4 more
wiley   +1 more source

Single‐Nucleus Multiomic Analyses Identifies Gene Regulatory Dynamics of Phenotypic Modulation in Human Aneurysmal Aortic Root

Advanced Science
Aortic root aneurysm is a potentially life‐threatening condition that may lead to aortic rupture and is often associated with genetic syndromes, such as Marfan syndrome (MFS).
Xuanyu Liu, Qingyi Zeng, Hang Yang, Wenke Li, Qianlong Chen, Kunlun Yin, Zihang Pan, Kai Wang, Mingyao Luo, Chang Shu, Zhou Zhou   +10 more
doaj   +1 more source

Management of a pregnant woman with Marfan syndrome and aortic root and aberrant right subclavian artery aneurysm: a case report [PDF]

Inga Voges, Ulrike Hoffmann, Tim Attman, Anselm Uebing   +3 more
openalex   +1 more source

Impact of surgically placed radiopaque markers during aortic root surgery on facilitating secondary diagnostic and therapeutic interventions [PDF]

, 2023
Emmanuel Zimmer, Maria Nucera, Clarence Pingpoh, Murat Yıldız, Paul Puiu, Florian Schoenhoff, Martin Czerny, Matthias Siepe   +7 more
openalex   +1 more source

Impact of Secondary Prevention on Mortality in the Building Trades National Medical Screening Program: Effectiveness of Occupational High‐Risk Management

American Journal of Industrial Medicine, EarlyView.
ABSTRACT Background Since 1997 the Building Trades National Medical Screening Program (BTMed) has offered medical exams to construction workers employed in US nuclear weapons facilities. The process consists of two steps: (1) a detailed work history interview; and (2) a medical exam.
Knut Ringen, John M. Dement, Marianne Cloeren, Sammy Almashat, William Grier, Stella Hines, Laura S. Welch, Kim Cranford, Scott Haas, Patricia Quinn, Anna Chen, Miles Fisher   +11 more
wiley   +1 more source

Syndrome of the Month: An Update on Smith‐Kingsmore Syndrome: Characterization of Developmental Milestones and a Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Smith‐Kingsmore syndrome (SKS) is a rare autosomal dominant condition characterized by neurodevelopmental differences, macrocephaly/megalencephaly, describable facial features, sleep–wake abnormalities, hyperphagia, and overgrowth. SKS is caused by pathogenic gain‐of‐function variants in MTOR which lead to hyperactivation of the mTOR pathway ...
Carolyn R. Raski, Carlos E. Prada
wiley   +1 more source

Marfan’s syndrome with aneurysmal formation of the aortic root and ascending aorta concomitant with aortic valve regurgitation of patients undergoing Bentall operation: the first two cases in southern Thailand

Journal of Health Science and Medical Research (JHSMR), 2004
The aorta is considered as pathologically dilated when the diameter of the aortic root and ascending aorta exceed the normal for a given age and body size.
V Chittithavorn, C Rergkliang, A Chetpaophan, P Vasinanukorn, T Chanchayanon, V Vasinwong, J Katayjan, S Suwanugsorn, V Chintapakorn   +8 more
doaj  

Aortic root reconstructive surgery - new created technique for aortic stenosis [PDF]

, 2012
Zan Mitrev, Tanja Anguseva, Emil Stoicovski, E Idoski   +3 more
openalex  

Graft Selection for Aortic Root Replacement in Complex Active Endocarditis: Does It Matter? [PDF]

, 2011
Arminder S. Jassar, Joseph E. Bavaria, Wilson Y. Szeto, Patrick Moeller, Jon Maniaci, Rita K. Milewski, Joseph H. Gorman, Nimesh D. Desai, Robert C. Gorman, Alberto Pochettino   +9 more
openalex   +1 more source

Marfan Syndrome Associated With Intellectual Disability and Behavioral Anomalies: Further Evidence for the Effect of Compound Heterozygous Variants in FBN1 on Phenotypic Severity

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Marfan syndrome (MFS) is a rare connective tissue disorder characterized by involvement of the cardiovascular, ocular, and musculoskeletal systems. Pathogenic variants in FBN1 cause most of the MFS cases; however, intellectual disability (ID) is rarely observed. A non‐consanguineous Pakistani family with four affected individuals was recruited.
Azmatullah Khan, Naseebullah Kakar, Ainullah Kakar, Malte Spielmann, Sajid Malik   +4 more
wiley   +1 more source