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American Heart Journal|June 1, 1990
Perioperative and long-term prognostic value of intravenous dipyridamole thallium scintigraphy in patients with peripheral vascular diseaseL T Younis, F Aguirre, S Byers, et al.
Molecular Genetics and Metabolism|January 27, 2005
Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophyStephan Kemp, Fredoen Valianpour, Simone Denis, et al.
Journal of Medical Genetics|September 1, 1995
The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studiesC Wallgren-Pettersson, A Clarke, F Samson, et al.
Ultrastructural Pathology|September 1, 1983
Ultrastructure of the liver in th cerebrohepatorenal syndrome of ZellwegerW J Mooi, K P Dingemans, M A van den Bergh Weerman, et al.
American Journal of Human Genetics|October 30, 1998
X chromosome inactivation in carriers of Barth syndromeK H Orstavik, R E Orstavik, A K Naumova, et al.
Neuromuscular Disorders : NMD|September 11, 2007
Rhabdomyolysis in pontocerebellar hypoplasia type 2 (PCH-2)Peter G Barth, Monique M Ryan, Richard I Webster, et al.
European Journal of Pediatrics|July 1, 1994
Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcificationsJ F Samson, P G Barth, J I de Vries, et al.
European Journal of Human Genetics : EJHG|March 4, 2011
TSEN54 mutations cause pontocerebellar hypoplasia type 5Yasmin Namavar, David Chitayat, Peter G Barth, et al.
European Journal of Pediatrics|September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha geneW Lissens, P Vreken, P G Barth, et al.
Journal of the Royal Society, Interface|December 19, 2008
Surface force spectroscopic point load measurements and viscoelastic modelling of the micromechanical properties of air flow sensitive hairs of a spider (Cupiennius salei)Michael E McConney, Clemens F Schaber, Michael D Julian, et al.
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