Wevers RA - Search Results

1

Proteomics approaches to study genetic and metabolic disorders.

Gloerich J, Wevers RA, Smeitink JA, van Engelen BG, van den Heuvel LP. Gloerich J, et al. Among authors: wevers ra. J Proteome Res. 2007 Feb;6(2):506-12. doi: 10.1021/pr060487w. J Proteome Res. 2007. PMID: 17269707 Review.

2

Maturation of mitochondrial and other isoenzymes of creatine kinase in skeletal muscle of preterm born infants.

Smeitink J, Ruitenbeek W, van Lith T, Sengers R, Trijbels F, Wevers R, Sperl W, de Graaf R. Smeitink J, et al. Ann Clin Biochem. 1992 May;29 ( Pt 3):302-6. doi: 10.1177/000456329202900309. Ann Clin Biochem. 1992. PMID: 1319128

3

van Engelen BG, Lamers KJ, Gabreels FJ, Wevers RA, van Geel WJ, Borm GF. van Engelen BG, et al. Among authors: wevers ra. Clin Chem. 1992 Jun;38(6):813-6. Clin Chem. 1992. PMID: 1375875

4

Paediatric cerebrotendinous xanthomatosis.

Wevers RA, Cruysberg JR, Van Heijst AF, Janssen-Zijlstra FS, Renier WO, Van Engelen BG, Tolboom JJ. Wevers RA, et al. J Inherit Metab Dis. 1992;15(3):374-6. doi: 10.1007/BF02435980. J Inherit Metab Dis. 1992. PMID: 1405473 No abstract available.

5

Mitochondrial creatine kinase containing crystals, creatine content and mitochondrial creatine kinase activity in chronic progressive external ophthalmoplegia.

Smeitink J, Stadhouders A, Sengers R, Ruitenbeek W, Wevers R, ter Laak H, Trijbels F. Smeitink J, et al. Neuromuscul Disord. 1992;2(1):35-40. doi: 10.1016/0960-8966(92)90024-z. Neuromuscul Disord. 1992. PMID: 1525556

6

A method for quantitative measurement of mitochondrial creatine kinase in human skeletal muscle.

Smeitink J, Wevers R, Hulshof J, Ruitenbeek W, van Lith T, Sengers R, Trijbels F, Korenke C, Wallimann T. Smeitink J, et al. Ann Clin Biochem. 1992 Mar;29 ( Pt 2):196-201. doi: 10.1177/000456329202900213. Ann Clin Biochem. 1992. PMID: 1626924

7

Cerebrospinal neuron-specific enolase, S-100 and myelin basic protein in neurological disorders.

Lamers KJ, van Engelen BG, Gabreëls FJ, Hommes OR, Borm GF, Wevers RA. Lamers KJ, et al. Among authors: wevers ra. Acta Neurol Scand. 1995 Sep;92(3):247-51. doi: 10.1111/j.1600-0404.1995.tb01696.x. Acta Neurol Scand. 1995. PMID: 7484080

8

Ocular and systemic manifestations of cerebrotendinous xanthomatosis.

Cruysberg JR, Wevers RA, van Engelen BG, Pinckers A, van Spreeken A, Tolboom JJ. Cruysberg JR, et al. Among authors: wevers ra. Am J Ophthalmol. 1995 Nov;120(5):597-604. doi: 10.1016/s0002-9394(14)72206-8. Am J Ophthalmol. 1995. PMID: 7485361

9

Metachromatic leukodystrophy: a 12-bp deletion in exon 2 of the arylsulfatase A gene in a late infantile variant.

Luyten JA, Wenink PW, Steenbergen-Spanjers GC, Wevers RA, Ploos van Amstel HK, de Jong JG, van den Heuvel LP. Luyten JA, et al. Among authors: wevers ra. Hum Genet. 1995 Sep;96(3):357-60. doi: 10.1007/BF00210424. Hum Genet. 1995. PMID: 7649558 Free article.

10

Mitochondrial creatine kinase activity in patients with disturbed energy generation in muscle mitochondria.

Smeitink J, Ruitenbeek W, Sengers R, Wevers R, van Lith T, Trijbels F. Smeitink J, et al. J Inherit Metab Dis. 1994;17(1):67-73. doi: 10.1007/BF00735397. J Inherit Metab Dis. 1994. PMID: 8051938

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