Bolhuis PA - Search Results

1

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.

De Vries DD, Went LN, Bruyn GW, Scholte HR, Hofstra RM, Bolhuis PA, van Oost BA. De Vries DD, et al. Among authors: bolhuis pa. Am J Hum Genet. 1996 Apr;58(4):703-11. Am J Hum Genet. 1996. PMID: 8644732 Free PMC article.

2

Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy.

Ginjaar HB, van der Kooi AJ, Ceelie H, Kneppers AL, van Meegen M, Barth PG, Busch HF, Wokke JH, Anderson LV, Bönnemann CG, Jeanpierre M, Bolhuis PA, Moorman AF, de Visser M, Bakker E, Ommen GJ. Ginjaar HB, et al. Among authors: bolhuis pa. J Neurol. 2000 Jul;247(7):524-9. doi: 10.1007/s004150070151. J Neurol. 2000. PMID: 10993494

3

Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.

Howell N, Oostra RJ, Bolhuis PA, Spruijt L, Clarke LA, Mackey DA, Preston G, Herrnstadt C. Howell N, et al. Among authors: bolhuis pa. Am J Hum Genet. 2003 Jun;72(6):1460-9. doi: 10.1086/375537. Epub 2003 May 6. Am J Hum Genet. 2003. PMID: 12736867 Free PMC article.

4

Reply to Hofmann et al.

Mackey D, Oostra RJ, Rosenberg T, Nikoskelainen E, Poulton J, Barratt T, Bolhuis P, Norby S, Savontaus ML, Chan C, Howell N. Mackey D, et al. Am J Hum Genet. 1998 Feb;62(2):492-5. doi: 10.1086/301731. Am J Hum Genet. 1998. PMID: 9463338 Free PMC article. No abstract available.

5

Regulation of the expression of mitochondrial proteins: relationship between mtDNA copy number and cytochrome-c oxidase activity in human cells and tissues.

Van den Bogert C, De Vries H, Holtrop M, Muus P, Dekker HL, Van Galen MJ, Bolhuis PA, Taanman JW. Van den Bogert C, et al. Among authors: bolhuis pa. Biochim Biophys Acta. 1993 Sep 13;1144(2):177-83. doi: 10.1016/0005-2728(93)90170-k. Biochim Biophys Acta. 1993. PMID: 8396443

6

Mitochondria in cultured human muscle cells depleted of mitochondrial DNA.

Herzberg NH, Middelkoop E, Adorf M, Dekker HL, Van Galen MJ, Van den Berg M, Bolhuis PA, Van den Bogert C. Herzberg NH, et al. Among authors: bolhuis pa. Eur J Cell Biol. 1993 Aug;61(2):400-8. Eur J Cell Biol. 1993. PMID: 8223726

7

Cultured human muscle cells and respiratory chain deficiencies.

Herzberg NH, Bolhuis PA, van den Bogert C, Barth PG. Herzberg NH, et al. Among authors: bolhuis pa. Neuromuscul Disord. 1994 Jan;4(1):3-11. doi: 10.1016/0960-8966(94)90042-6. Neuromuscul Disord. 1994. PMID: 8173349 Review.

8

Altered kinetics of cytochrome c oxidase in a patient with severe mitochondrial encephalomyopathy.

Nijtmans LG, Barth PG, Lincke CR, Van Galen MJ, Zwart R, Klement P, Bolhuis PA, Ruitenbeek W, Wanders RJ, Van den Bogert C. Nijtmans LG, et al. Among authors: bolhuis pa. Biochim Biophys Acta. 1995 Apr 24;1270(2-3):193-201. doi: 10.1016/0925-4439(95)00044-5. Biochim Biophys Acta. 1995. PMID: 7727543 Free article.

9

Major growth reduction and minor decrease in mitochondrial enzyme activity in cultured human muscle cells after exposure to zidovudine.

Herzberg NH, Zorn I, Zwart R, Portegies P, Bolhuis PA. Herzberg NH, et al. Among authors: bolhuis pa. Muscle Nerve. 1992 Jun;15(6):706-10. doi: 10.1002/mus.880150613. Muscle Nerve. 1992. PMID: 1324428

10

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts.

Barth PG, Van den Bogert C, Bolhuis PA, Scholte HR, van Gennip AH, Schutgens RB, Ketel AG. Barth PG, et al. Among authors: bolhuis pa. J Inherit Metab Dis. 1996;19(2):157-60. doi: 10.1007/BF01799418. J Inherit Metab Dis. 1996. PMID: 8739954 Free article. No abstract available.

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