OAR@UM Collection:/library/oar/handle/123456789/35882026-06-12T04:42:50Z2026-06-12T04:42:50ZMitral valve prolapse and mitral insufficiency in two siblings with Gaucher's diseaseCelik, S.Erdol, CevdetBaykan, MerihOrem, CihanGokce, M.Durmus, Ismet/library/oar/handle/123456789/37992018-08-13T10:37:33Z2000-01-01T00:00:00ZTitle: Mitral valve prolapse and mitral insufficiency in two siblings with Gaucher's disease
Authors: Celik, S.; Erdol, Cevdet; Baykan, Merih; Orem, Cihan; Gokce, M.; Durmus, Ismet
Abstract: Gaucher's disease is an autosomal recessive storage disorder. This article reports two
siblings with Gaucher's disease, both of which had mitral valve prolapse and mitral
insufficiency. One of the siblings died of bacterial endocarditis and pneumonia, while
the other continues under followup.2000-01-01T00:00:00ZImages in paediatric cardiology : no longer an infant!/library/oar/handle/123456789/37732015-07-02T01:03:54Z2000-01-01T00:00:00ZTitle: Images in paediatric cardiology : no longer an infant!
Abstract: This editorial is written on the first anniversary of the Journal 'Images in Paediatric Cardiology.' It discusses the progress of the journal and the issues it faces regarding peer-review, copyright and publication concerns.2000-01-01T00:00:00ZVentricular septal defects : morphology of the doubly committed juxtaarterial and muscular variantsMcCarthy, KarenHo, Siew YenAnderson, Robert H./library/oar/handle/123456789/37712018-08-20T10:56:47Z2000-01-01T00:00:00ZTitle: Ventricular septal defects : morphology of the doubly committed juxtaarterial and muscular variants
Authors: McCarthy, Karen; Ho, Siew Yen; Anderson, Robert H.
Abstract: A previous review of the phenotypic features of ventricular septal defects,
concentrated on the perimembranous variant, showing how its distinguishing feature,
as viewed from the right ventricle, was fibrous continuity in its postero-inferior rim
between the leaflets of the aortic and tricuspid valves. In this second review, the
focus is on the morphology of those defects which have exclusively muscular rims
when viewed from their right side, and the variant with the phenotypic feature of
fibrous continuity between the leaflets of the two arterial valves. As with the defects
described as being perimembranous, once they have been characterised, it is the
position of the defect relative to the components of the morphologically right ventricle
that is the primary determinant of the options and strategies for treatment. Therefore,
clarification of the morphology is the key to establishing the related risks for each
particular defect.2000-01-01T00:00:00ZIsolated right pulmonary artery discontinuityTurner, DanielVincent, J.A.Epstein, M.L./library/oar/handle/123456789/37692015-07-02T01:04:46Z2000-01-01T00:00:00ZTitle: Isolated right pulmonary artery discontinuity
Authors: Turner, Daniel; Vincent, J.A.; Epstein, M.L.
Abstract: Unilateral “absence” of the pulmonary artery is an uncommon malformation
frequently associated with congenital heart disease. In fact, the pulmonary artery is
typically discontinuous from the main pulmonary artery, not absent. This article reports a case of right pulmonary artery discontinuity not associated with congenital heart disease
and reviews the embryogenesis and treatment of this rare congenital cardiac anomaly.2000-01-01T00:00:00Z