Natural history of Barth syndrome: a national cohort study of 22 patients

Barth syndrome

(2013) Sarah LN Clarke et al.   Orphanet Journal of Rare Diseases

The Barth Syndrome Registry: Distinguishing disease characteristics and growth data from a longitudinal study

(2012) Amy E. Roberts et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Barth syndrome in a female patient

(2012) Laure Cosson et al.   MOLECULAR GENETICS AND METABOLISM

Left Ventricular Noncompaction Cardiomyopathy in Barth Syndrome: An Example of an Undulating Cardiac Phenotype Necessitating Mechanical Circulatory Support as a Bridge to Transplantation

(2012) Samuel P. Hanke et al.   PEDIATRIC CARDIOLOGY

Síndrome de Barth en la edad adulta: un caso clínico

(2012) María Sabater-Molina et al.   REVISTA ESPANOLA DE CARDIOLOGIA

Impaired cardiac reserve and severely diminished skeletal muscle O2 utilization mediate exercise intolerance in Barth syndrome

(2011) Carolyn T. Spencer et al.   AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY

Eponym

(2011) Atsuhito Takeda et al.   EUROPEAN JOURNAL OF PEDIATRICS

Congenital neutropenia: diagnosis, molecular bases and patient management

(2011) Jean Donadieu et al.   Orphanet Journal of Rare Diseases

Gonadal mosaicism of a TAZ (G4.5) mutation in a Japanese family with Barth syndrome and left ventricular noncompaction

(2010) Bo Chang et al.   MOLECULAR GENETICS AND METABOLISM

Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth

(2010) C. G. Steward et al.   PRENATAL DIAGNOSIS

Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography–mass spectrometry as a diagnostic test for Barth syndrome

(2009) Riekelt H. Houtkooper et al.   ANALYTICAL BIOCHEMISTRY

Dysmorphology of Barth syndrome

(2009) Rob Hastings et al.   CLINICAL DYSMORPHOLOGY

New indications and controversies in arginine therapy

(2008) David Coman et al.   CLINICAL NUTRITION