Results 181 to 190 of about 303,973 (343)

Cardiac magnetic resonance imaging-large language model Meta AI: a finetuned large language model for identifying findings and associated attributes in cardiac magnetic resonance imaging reports. [PDF]

J Cardiovasc Magn Reson
Fang MZ, Nakashima M, Singh K, Galvani E, Sun X, Sorathia S, Dorocak K, Kwon D, Nguyen C, Chen D.   +9 more
europepmc   +1 more source

Quantification of Cardiac Output with Phase Contrast Magnetic Resonance Imaging in Patients with Pulmonary Hypertension

, 2020
Jose Ricardo Po, Matthew Tong, Talha Meeran, Alekhya Potluri, Amresh Raina, Mark Doyle, Robert W Biederman   +6 more
openalex   +2 more sources

Cardiac Magnetic Resonance Imaging Findings in 20-year Survivors of Mediastinal Radiotherapy for Hodgkin's Disease [PDF]

, 2010
Wolfram Machann, Meinrad Beer, M Breunig, Stefan Störk, Christiane Angermann, Ines Seufert, F. Schwab, Oliver Kölbl, Michael Flentje, Dirk Vordermark   +9 more
openalex   +1 more source

Expanding the Genotype–Phenotype Correlation of Marden–Walker Syndrome due to PIEZO2 Gene Variants: A Case Report From Brazil

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Marden–Walker syndrome (MWS; OMIM 248700) is an extremely rare congenital disorder characterized by multiple joint contractures, craniofacial dysmorphism, neurological abnormalities, and multisystem involvement. Although historically diagnosed on clinical grounds, only a few cases have been molecularly confirmed.
Guilherme Sotto Battiston, Carolina de Souza Araujo, Fernanda Araujo Romera, André Luis Ferreira, Érica Trovisco Martins, Carolina Galhós de Aguiar, José Eduardo Mourão Santos, Rodrigo Ragazzini, Daniela Testoni Costa‐Nobre, Ana Claudia Yoshikumi Prestes, Allan Chiaratti de Oliveira, Eduardo Perrone, Débora Gusmão Melo, Anne Caroline Barbosa Teixeira, Antonio Victor Campos Coelho, Caio Robledo D’Angioli Costa Quaio, Carolina Araujo Moreno, Eduardo Perrone, Jose Bandeira do Nascimento Junior, Jessica Grasiela Araujo Espolaor, Joana Rosa Marques Prota, Joao Bosco de Oliveira Filho, Jose Ricardo Magliocco Ceroni, Kelin Chen, Letícia Torres Ferreira, Lucas Santos de Santana, Luciana Souto Mofatto, Luiza do Amaral Virmond, Marina de Franca Basto Silva, Michele Patricia Migliavacca, Renata Moldenhauer Minillo, Renata Yoshiko Yamada, Roberta Sitnik, Tatiana Ferreira de Almeida, Thiago Yoshinaga Tonholo Silva, Vivian Pedigone Cintra   +35 more
wiley   +1 more source

Beyond ejection fraction: cardiac magnetic resonance imaging in anthracycline cardiotoxicity. [PDF]

BMC Med Imaging
Motevalli M, Deilami T, Kia YM, Poopak A, Houshmand G.   +4 more
europepmc   +1 more source

‘New World’ imaging for an ‘Old World’ disease: Use of cardiac magnetic resonance imaging and 3D transesophageal echocardiography in severe rheumatic mitral valve disease [PDF]

, 2012
Ravin L. Ramtohal, Peter O’Kane, J Radvan, Russell Bull, Chandrike Ponnamperuma, Sarah K. George   +5 more
openalex   +1 more source

Impact of Rapid Exome Sequencing on Pediatric Patients With Cardiomyopathy and Acute Heart Failure

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Few studies describe the impact of rapid exome sequencing (ES) on pediatric cardiomyopathy in urgent clinical settings. Here, we retrospectively report the impact of rapid singleton ES in pediatric patients presented with acute heart failure and isolated cardiomyopathy or myocarditis, between 2021 and 2023 at a single tertiary care center.
Tameemi Abdalla Moady, Tova Hershkovitz, Clair Habib, Ori Attias, Amir Hadash, Galit Tal, Asaad Khoury, Josef Ben‐Ari, Danny Eytan, Tamar Paperna, Karin Weiss   +10 more
wiley   +1 more source

Cardiac Magnetic Resonance Imaging in Heart Failure With Preserved Ejection Fraction. [PDF]

Circ Cardiovasc Imaging
Kikuchi DS, Quinaglia T, Bukhari S, Sharma K, Coelho-Filho OR, Hays AG.   +5 more
europepmc   +1 more source

Unveiling a New Link: Cholesterol Deficiency in Smith–Lemli–Opitz and Niemann–Pick C as a Driver of Ciliopathies

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The ciliopathies are a group of genetic disorders caused by defective function of either the primary cilia (a large number) or the motile cilia (a much smaller number). These have been defined as diseases with mutations in genes encoding individual ciliary or cilia‐associated proteins.
Robert P. Erickson, Maria Teresa Fiorenza   +1 more
wiley   +1 more source

Autoregressive report generation for cardiac magnetic resonance imaging

Makiya Nakashima, Po‐Hao Chen, Michael A. Bolen, Richard A. Grimm, W.H. Wilson Tang, Christopher Nguyen, Deborah Kwon, David Chen   +7 more
openalex   +1 more source