Results 91 to 100 of about 190,394 (243)

Predictors of Unfavourable Outcomes in Children and Adolescents Submitted to Surgical Mitral Valvuloplasty Secondary to Chronic Rheumatic Heart Disease

open access: yesArquivos Brasileiros de Cardiologia
Background: Mitral valve repair in paediatric patients with chronic rheumatic heart disease is superior to valve replacement and has been used with good results.
Renata Cristina Castro Cruz   +5 more
doaj   +1 more source

THE SURGICAL CORRECTION OF MITRAL INSUFFICIENCY

open access: yesJournal of Thoracic Surgery, 1954
SUMMARY 1. A morphologic classification of the pathology of mitral insufficiency is presented. 2. Some cardinal features of the kinetic pathology are described. 3. Various techniques that have been tried in other clinics to correct mitral insufficiency are reviewed. 4.
D E, HARKEN   +3 more
openaire   +3 more sources

Functional mitral stenosis in patients with massive mitral annular calcification.

open access: yes, 1981
Mitral insufficiency with mitral annular calcification occurring predominantly in elderly females has been described. We studied six patients with mitral diastolic obstruction associated with mitral annular calcification without stenosis of the mitral ...
L E Osterberger   +3 more
core   +1 more source

Prolapsus mitral : une étiologie méconnue d’arythmie ventriculaire et de mort subite [Mitral valve prolapse: beyond mitral regurgitation, the arrhythmic risk]

open access: yes, 2021
Mitral prolapse is a common condition, defined by the systolic bulging of at least one mitral leaflet into the left atrium, which is often accompanied by various degree of mitral insufficiency.
Monney, P.   +5 more
core   +1 more source

Standardized Reporting of Cardiac Magnetic Resonance Examinations in Children With Cardiac Diseases and Adults With Congenital Heart Disease: A Scientific Statement From the Association for European Pediatric and Congenital Cardiology (AEPC) and the International Society for Magnetic Resonance in Medicine (ISMRM)

open access: yes
Journal of Magnetic Resonance Imaging, EarlyView.
Francesca Raimondi   +26 more
wiley   +1 more source

Diagnostic Delay in Eosinophilic Granulomatosis With Polyangiitis: Clinical Predictors and Implications for Earlier Recognition

open access: yesAllergy, EarlyView.
This study aimed to assess diagnostic delay among patients with eosinophilic granulomatosis with polyangiitis (EGPA) and identify clinical characteristics associated with delayed recognition. EGPA diagnosis was delayed by nearly five years from symptom onset in this single‐center cohort.
Vani Mulkareddy   +9 more
wiley   +1 more source

Mitral valve prolapse and mitral insufficiency in two siblings with Gaucher's disease

open access: yes, 2000
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.
Gokce, M.   +5 more
core  

Assessing a Model for a Complex Systemic Disorder—The Value of Male Mice With a Supernumerary X Chromosome for Klinefelter Syndrome Research

open access: yesAndrology, EarlyView.
ABSTRACT Introduction Direct experimental investigation of Klinefelter syndrome (KS) in patients is limited because the syndrome manifests heterogeneously and affects multiple organ systems. Studying KS therefore requires a model that captures this complexity as accurately as possible while still permitting controlled experimental manipulation ...
Fariba Saadati, Joachim Wistuba
wiley   +1 more source

Conservative surgical management of mitral insufficiency: an alternative approach Tratamento cirúrgico conservador da insuficiência mitral: uma abordagem alternativa

open access: yes, 2012
Mitral valve insufficiency is frequently the result of elongated or ruptured chordae tendineae. Several techniques have been described for its correction.
Francisco Gregori Junior   +1 more
core   +1 more source

Genetic Testing Unveils a Novel Thrombospondin‐1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79‐Year‐Old Woman

open access: yesClinical Genetics, EarlyView.
A 79‐year‐old woman with lifelong peripheral edema and an affected sister was found to harbor a novel homozygous THSD1 splice‐site variant. Reduced THSD1 expression in dermal endothelial cells supported the possibility that this variant contributes to chronic hereditary edema.
Eiko Amo   +23 more
wiley   +1 more source

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