X-Linked Cardiac Valvular Dysplasia Latest Advances

A Novel In-Frame Deletion of FLNA in X-Linked Cardiac Valvular Dysplasia With Variable Clinical Spectrum.

Journal: Congenital anomalies

Published: October 10, 2025

A rare case of Kallmann syndrome in a female with pulmonary valve stenosis: Coincidence or genetic link?

Journal: La Tunisie medicale

Published: January 22, 2025

X-linked myxomatous valvular dystrophy in a patient with a novel mutation in the FLNA gene.

Journal: Kardiologia polska

Published: December 23, 2022

In-frame Variants in FLNA Proximal Rod 1 Domain Associate With a Predominant Cardiac Valvular Phenotype.

Journal: Revista espanola de cardiologia (English ed.)

Published: July 06, 2017

Congenital valvular defects associated with deleterious mutations in the PLD1 gene.

Journal: Journal of medical genetics

Published: August 20, 2016

Longitudinal Echocardiographic Evaluation of an Unusual Presentation of X-Linked Myxomatous Valvular Dystrophy Caused by Filamin A Mutation.

Journal: Seminars in cardiothoracic and vascular anesthesia

Published: March 24, 2016

Surgical experience for prolapse of both atrioventricular valves in a patient with filamin A mutation.

Journal: Cardiology in the young

Published: February 14, 2014

Mitral valve regurgitation: use of the standard and the latest echocardiographic techniques for establishing the diagnosis.

Journal: Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese

Published: September 22, 2012

A familial case of Cantu craniofaciofronto digital syndrome.

Journal: Clinical dysmorphology

Published: April 17, 2012

Warfarin embryopathy: fetal manifestations.

Journal: Virchows Archiv : an international journal of pathology

Published: March 01, 2010

On the diagnosis of congenital valvular heart diseases

Journal: Zeitschrift fur Kreislaufforschung

Published: January 01, 1952

X-Linked Cardiac Valvular Dysplasia Latest Advances

Find the Latest Research About X-Linked Cardiac Valvular Dysplasia

A Novel In-Frame Deletion of FLNA in X-Linked Cardiac Valvular Dysplasia With Variable Clinical Spectrum.

A Novel In-Frame Deletion of FLNA in X-Linked Cardiac Valvular Dysplasia With Variable Clinical Spectrum.

A rare case of Kallmann syndrome in a female with pulmonary valve stenosis: Coincidence or genetic link?

A rare case of Kallmann syndrome in a female with pulmonary valve stenosis: Coincidence or genetic link?

X-linked myxomatous valvular dystrophy in a patient with a novel mutation in the FLNA gene.

X-linked myxomatous valvular dystrophy in a patient with a novel mutation in the FLNA gene.

In-frame Variants in FLNA Proximal Rod 1 Domain Associate With a Predominant Cardiac Valvular Phenotype.

In-frame Variants in FLNA Proximal Rod 1 Domain Associate With a Predominant Cardiac Valvular Phenotype.

Congenital valvular defects associated with deleterious mutations in the PLD1 gene.

Congenital valvular defects associated with deleterious mutations in the PLD1 gene.

Longitudinal Echocardiographic Evaluation of an Unusual Presentation of X-Linked Myxomatous Valvular Dystrophy Caused by Filamin A Mutation.

Longitudinal Echocardiographic Evaluation of an Unusual Presentation of X-Linked Myxomatous Valvular Dystrophy Caused by Filamin A Mutation.

Surgical experience for prolapse of both atrioventricular valves in a patient with filamin A mutation.

Surgical experience for prolapse of both atrioventricular valves in a patient with filamin A mutation.

Mitral valve regurgitation: use of the standard and the latest echocardiographic techniques for establishing the diagnosis.

Mitral valve regurgitation: use of the standard and the latest echocardiographic techniques for establishing the diagnosis.

A familial case of Cantu craniofaciofronto digital syndrome.

A familial case of Cantu craniofaciofronto digital syndrome.

Warfarin embryopathy: fetal manifestations.

Warfarin embryopathy: fetal manifestations.

On the diagnosis of congenital valvular heart diseases

On the diagnosis of congenital valvular heart diseases