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Proceedings. Biological Sciences|January 26, 2007
Spitting out information: Trigona bees deposit saliva to signal resource locationsDirk Louis P Schorkopf, Stefan Jarau, Wittko Francke, et al.Journal of Neuropathology and Experimental Neurology|September 1, 1993
Ependymal abnormalities in lissencephaly/pachygyriaH B Sarnat, H Z Darwish, P G Barth, et al.Neuropediatrics|July 13, 1999
Pontocerebellar hypoplasia associated with respiratory-chain defectsT J de Koning, L S de Vries, F Groenendaal, et al.Neurology|December 11, 2002
Biochemical markers predicting survival in peroxisome biogenesis disordersJ Gootjes, P A W Mooijer, C Dekker, et al.Neuropediatrics|June 1, 1993
Molybdenum-cofactor deficiency: an easily missed cause of neonatal convulsionsH M Slot, W C Overweg-Plandsoen, H D Bakker, et al.Acta Neuropathologica|July 21, 2007
Pontocerebellar hypoplasia type 2: a neuropathological updatePeter G Barth, Eleonora Aronica, Linda de Vries, et al.Tijdschrift Voor Kindergeneeskunde|October 1, 1989
[X-linked adrenoleukodystrophy and other peroxisomal diseases caused by a failing peroxisomal beta-oxidation system: clinical expression, diagnosis and treatment]R J Wanders, P G Barth, R B Schutgens, et al.Molecular Genetics and Metabolism|April 20, 2006
High incidence of hyperoxaluria in generalized peroxisomal disordersChristiaan S van Woerden, Jaap W Groothoff, Frits A Wijburg, et al.Neurology|April 1, 1997
A new leukoencephalopathy with vanishing white matterM S van der Knaap, P G Barth, F J Gabreëls, et al.European Journal of Pediatrics|July 1, 1985
Cerebral gigantism (Sotos syndrome). Compiled data of 22 cases. Analysis of clinical features, growth and plasma somatomedinJ M Wit, F A Beemer, P G Barth, et al.Pageof 30