Results 151 to 160 of about 205,036 (308)

A safe and simple method of preserving right ventricular function during implantation of a left ventricular assist device [PDF]

, 2001
Matthias Loebe, Evgenij Potapov, Ralf Sodian, Michael Kopitz, George P. Noon   +4 more
openalex   +1 more source

E‐CAD: Electroactive Polymer‐Based Cardiac Assist Device with Low Power Consumption

Advanced Intelligent Systems, EarlyView.
Conventional cardiac assist devices often require high power, involve direct blood contact, and risk driveline infections. This work presents a soft electroactive polymer‐based system that compresses the heart externally while consuming <0.3 W. With no blood contact, a 0.3 mm driveline, and a compact design, E‐CAD demonstrates enhanced output and ...
Jiyeop Kim, Junheon Lee, Sein Song, Si‐Hyuck Kang, Amy Kyungwon Han   +4 more
wiley   +1 more source

Right Ventricular Function and Afterload Following Novel Transcatheter Tricuspid Valve Replacement. [PDF]

JACC Case Rep
Kempton H, Namasivayam M, Meredith T, Shaw M, Jansz P, Muller DWM.   +5 more
europepmc   +1 more source

Huge right ventricle–right coronary artery fistula compromising right ventricular function in a patient with pulmonary atresia and intact ventricular septum: A case report [PDF]

, 2001
Masamichi Ono, Shigeaki Otake, Norihide Fukushima, Yoshiki Sawa, Hajime Ichikawa, Koji Kagisaki, Hikaru Matsuda   +6 more
openalex   +1 more source

Sickle Cell Diastolic Cardiomyopathy and Mortality Risk: A Novel Echocardiographic Framework for Prognostic Stratification

American Journal of Hematology, EarlyView.
ABSTRACT Cardiovascular complications are the leading cause of mortality in sickle cell anemia (SCA) patients. While extensive data have identified diastolic dysfunction (DD) to increase morbidity and mortality, the unique hemodynamic conditions inherent to SCA challenge the current recommendations to assess diastolic function. Thus, there is an urgent
Théo Simon, Laurent Savale, Kristoffer Grundtvig Skaarup, Paul Breillat, Luu‐Ly Pham, Seyed‐Mehdi Nouraie, Niklas Dyrby Johansen, Jocelyn Inamo, Francois Lionnet, Gylna Loko, Christelle Chantalat, Anne Laure Pham Hung d’Alexandry d’Orengiani, Anoosha Habibi, Gonzalo de Luna, Sihem Iles, Frédéric Galactéros, Etienne Audureau, Tor Biering‐Sørensen, Pablo Bartolucci, Geneviève Derumeaux, Thomas d’Humières   +20 more
wiley   +1 more source

A longitudinal study of right ventricular function of patients with multiple myeloma treated with carfilzomib. [PDF]

ERJ Open Res
Basin S, Cezar M, Fraix A, Pace N, Filippetti L, Schulmann S, Selton-Suty C, Huttin O, Chabot F, Chaouat A, Valentin S.   +10 more
europepmc   +1 more source

Deterioration of left ventricular function following atrio-ventricular node ablation and right ventricular apical pacing in patients with permanent atrial fibrillation [PDF]

, 2001
Tamás Szili‐Törok, GK Kimman, RAP Borghans, Aggie H.M.M. Balk, Jrtc Roelandt, Luc Jordaens   +5 more
openalex   +1 more source

Phenotypic Characterization of Seven Pediatric Patients Diagnosed With KAT6B‐Related Disorders: Case Series and Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genitopatellar syndrome (GPS) and Say‐Barber‐Biesecker‐Young‐Simpson Syndrome (SBBYSS) are clinically distinct neurodevelopmental disorders caused by monoallelic pathogenic variants in KAT6B. In some cases, GPS and SBBYSS features can overlap, determining an intermediate phenotype.
Vittorio Maglione, Antonio Pizzuti, Gioia Mastromoro, Eleonora Cresta, Paola Favata, Maria Cristina Digilio, Rossella Capolino, Maria Lisa Dentici, Lorenzo Sinibaldi, Antonio Novelli, Marco Tartaglia, Gianluca Terrin, Viviana Cardilli   +12 more
wiley   +1 more source

Anterior Chordal Transection Impairs Not Only Regional Left Ventricular Function But Also Regional Right Ventricular Function in Mitral Regurgitation [PDF]

, 2001
Thierry Le Tourneau, Daniel Grandmougin, C. Foucher, Eugène McFadden, Pascal de Groote, Alain Prat, H Warembourg, Ghislaine Deklunder   +7 more
openalex   +1 more source

Case Report: Unusual Neurological Features of Leigh Syndrome due to m.8993T>G Pathogenic Variant in the MT‐ATP6 Gene

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The MT‐ATP6 gene m.8993T>G pathogenic variant has been associated with Leigh syndrome, especially in patients exhibiting a high degree of heteroplasmy. Although patients may present with a wide phenotypic spectrum, characteristic findings include bilateral, symmetric hyperintensities in the basal ganglia and brainstem on brain MRI ...
Ramya Treitel, Julie McLaughlin, Marta Frigeni   +2 more
wiley   +1 more source