Results 231 to 240 of about 546,461 (357)

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

open access: yesAdvanced 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   +4 more
wiley   +1 more source

Effects of chronic volume deprivation on the ventricle. [PDF]

open access: yesInterdiscip Cardiovasc Thorac Surg
Cools B   +8 more
europepmc   +1 more source

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

open access: yesAmerican 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   +12 more
wiley   +1 more source

Inadvertent temporary transvenous pacing of the left ventricle: an underreported complication-a case report. [PDF]

open access: yesEur Heart J Case Rep
Pathangey G   +4 more
europepmc   +1 more source

Prenatal Brain Abnormalities in Sodium‐Dependent Multivitamin Transporter Deficiency

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT In treatable neurometabolic disorders, early diagnosis and prompt initiation of treatment are key to improved survival and outcomes. Biallelic variants in SLC5A6 cause sodium‐dependent multivitamin transporter deficiency (OMIM # 618973), which is treatable with high‐dose pantothenic acid, biotin, and alpha lipoic acid.
Eri Ogawa   +2 more
wiley   +1 more source

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

open access: yesAmerican 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   +2 more
wiley   +1 more source

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