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Acta Endocrinologica|June 1, 1983
Uptake of triiodothyronine into cultured human muscle cellsP A Bolhuis, C van den Berg, N J Ponne, et al.Brain : a Journal of Neurology|December 1, 1995
Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein geneW A van Gool, G W Hensels, E M Hoogerwaard, et al.Biochemical and Biophysical Research Communications|October 24, 1995
The mitochondrial DNA mutation ND6*14,484C associated with leber hereditary optic neuropathy, leads to deficiency of complex I of the respiratory chainR J Oostra, M J Van Galen, P A Bolhuis, et al.Human Genetics|September 1, 1994
Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutationR J Oostra, P A Bolhuis, I Zorn-Ende, et al.Journal of Applied Microbiology|April 26, 2021
A requirement for flow to enable the development of Ureaplasma parvum biofilms in vitroR S Rowlands, K Kragh, S Sahu, et al.Molecular & General Genetics : MGG|November 27, 1996
A general system for generating unlabelled gene replacements in bacterial chromosomesK Leenhouts, G Buist, A Bolhuis, et al.Acta Neuropathologica|January 1, 1993
Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteriaA A Gabreëls-Festen, F J Gabreëls, J E Hoogendijk, et al.Acta Neuropathologica|January 1, 1995
Charcot-Marie-Tooth disease type 1A: morphological phenotype of the 17p duplication versus PMP22 point mutationsA A Gabreëls-Festen, P A Bolhuis, J E Hoogendijk, et al.Cytogenetics and Cell Genetics|January 1, 1988
Regional localization of the gene for thyroid peroxidase to human chromosome 2pter----p12J J de Vijlder, C Dinsart, F Libert, et al.Pediatric Research|July 1, 1988
Receptor-mediated uptake of acid alpha-glucosidase corrects lysosomal glycogen storage in cultured skeletal muscleA T Van der Ploeg, M C Loonen, P A Bolhuis, et al.Pageof 14