Syndrome de Barth (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Syndrome de Barth" in French language version.

refsWebsite

Global rank French rank

2sciencedirect.com

149^th place

80^th place

1biomedcentral.com

2,747^th place

1,253^rd place

1aappublications.org

3,763^rd place

2,725^th place

222^nd place

129^th place

234^th place

147^th place

1frontiersin.org

4,679^th place

1,649^th place

aappublications.org

pediatrics.aappublications.org

Spencer CT, Bryant RM, Day J et al. Cardiac and clinical phenotype in Barth syndrome, Pediatrics, 2006;118:e337–e346

biomedcentral.com

ojrd.biomedcentral.com

Clarke SL, Bowron A, Gonzalez IL et al. Barth syndrome, Orphanet J Rare Dis, 2013;8:23

frontiersin.org

Saric A, Andreau K, Armand AS, Møller IM, Petit PX, Barth syndrome: from mitochondrial dysfunctions associated with aberrant production of reactive oxygen species to pluripotent stem cell studies, Front Genet 2015;6:359

nature.com

Bione S, D’Adamo P, Maestrini E, Gedeon AK, Bolhuis PA, Toniolo D, A novel X-linked gene, G4.5. is responsible for Barth syndrome, Nat Genet, 1996;12:385–389

sciencedirect.com

Barth PG, Scholte HR, Berden JA et al. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes, J Neurol Sci, 1983; 62:327–355
Bleyl SB, Mumford BR, Thompson V et al. « Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome », Am J Hum Genet, 1997;61:868–872

wiley.com

onlinelibrary.wiley.com

Roberts AE, Nixon C, Steward CG ar al. The Barth Syndrome Registry: distinguishing disease characteristics and growth data from a longitudinal study, Am J Med. Genet A. 2012;158A:2726–2732