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American Journal of Medical Genetics|July 1, 1991
Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibshipD B van Dorp, A Palan, M L Kwee, et al.European Journal of Pediatrics|January 1, 1985
An infant with Marfanoid phenotype and congenital contractures associated with ocular and cardiovascular anomalies, cerebral white matter hypoplasia and spinal axonopathyP Tamminga, F G Jennekens, P G Barth, et al.Neurology|August 26, 1998
Phenotypic variation in leukoencephalopathy with vanishing white matterM S van der Knaap, W Kamphorst, P G Barth, et al.Neuropediatrics|May 6, 2004
The spectrum of cranial ultrasound and magnetic resonance imaging abnormalities in congenital cytomegalovirus infectionL S de Vries, H Gunardi, P G Barth, et al.Neuropediatrics|August 1, 1996
Cerebellar hypoplasia in respiratory chain dysfunctionC R Lincke, C van den Bogert, L G Nijtmans, et al.Acta Paediatrica (Oslo, Norway : 1992)|February 1, 1996
Going Dutch in nocturnal enuresisT W Schulpen, R A Hirasing, T P de Jong, et al.Journal of Lipid Research|February 4, 2003
Linoleic acid supplementation of Barth syndrome fibroblasts restores cardiolipin levels: implications for treatmentF Valianpour, R J A Wanders, H Overmars, et al.Biochemical and Biophysical Research Communications|December 19, 2000
Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndromeP Vreken, F Valianpour, L G Nijtmans, et al.Journal of the Neurological Sciences|December 1, 1988
Peroxisomal disorders in neurologyR J Wanders, H S Heymans, R B Schutgens, et al.AJNR. American Journal of Neuroradiology|January 19, 2006
Sequential MR imaging changes in nonketotic hyperglycinemiaJ Mourmans, C B L M Majoie, P G Barth, et al.Pageof 23