Results 171 to 180 of about 2,742,983 (330)

Essential Modifiers of Double Outlet Right Ventricle: Revisit With Endocardial Surface Images and 3-Dimensional Print Models.

open access: yesCirculation Cardiovascular Imaging, 2018
D. Yim   +6 more
semanticscholar   +1 more source

Forgotten No More: A Focused Update on the Right Ventricle in Cardiovascular Disease.

open access: yesJACC. Heart failure, 2018
M. Amsallem   +4 more
semanticscholar   +1 more source

Transcriptional Signatures of the Right Ventricle in End-Stage Heart Failure. [PDF]

open access: yesPulm Circ
Garry JD   +9 more
europepmc   +1 more source

Echocardiographic Assessment of the Right Ventricle-State of the Art.

open access: yesHeart, Lung and Circulation, 2019
N. Jones, A. Burns, D. Prior
semanticscholar   +1 more source

Complex Management of Thromboembolism in Double-Outlet Right Ventricle. [PDF]

open access: yesJACC Case Rep
Bhargava P   +5 more
europepmc   +1 more source

Children With 22.Q.11.2 Deletion Syndrome: Sleep‐Disordered Breathing and Management

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Patients with 22q11.2 deletion syndrome (22q11DS) are predisposed to obstructive sleep apnea (OSA) due to an abnormal craniofacial anatomy with pharyngeal hypotonia, retrognathia, micrognathia, and glossoptosis. The aim of the study was to describe the prevalence and management of OSA in a cohort of children with 22q11DS.
Domenico Paolo La Regina   +6 more
wiley   +1 more source

Bone cement embolism causing right ventricle perforation. [PDF]

open access: yesBMC Cardiovasc Disord
Dai X, Chen L, Pan D, Zhao H, Ma L.
europepmc   +1 more source

Profound Thrombocytopenia and Dyspnea 11 Days After Cardiac Surgery

open access: yes
American Journal of Hematology, EarlyView.
Sebastian Vuong   +3 more
wiley   +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

An anatomical review of the right ventricle

open access: yesTranslational Research in Anatomy, 2019
J. Wang   +7 more
semanticscholar   +1 more source

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