van den Heuvel LP - Search Results

1

Mapping of the human Voltage-Dependent Anion Channel isoforms 1 and 2 reconsidered.

Messina A, Oliva M, Rosato C, Huizing M, Ruitenbeek W, van den Heuvel LP, Forte M, Rocchi M, De Pinto V. Messina A, et al. Among authors: van den heuvel lp. Biochem Biophys Res Commun. 1999 Feb 24;255(3):707-10. doi: 10.1006/bbrc.1998.0136. Biochem Biophys Res Commun. 1999. PMID: 10049775

2

Characterization of the human porin isoform 1 (HVDAC1) gene by amplification on the whole human genome: A tool for porin deficiency analysis.

Messina A, Guarino F, Oliva M, van den Heuvel LP, Smeitink J, De Pinto V. Messina A, et al. Among authors: van den heuvel lp. Biochem Biophys Res Commun. 2000 Apr 21;270(3):787-92. doi: 10.1006/bbrc.2000.2487. Biochem Biophys Res Commun. 2000. PMID: 10772903

3

Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy.

Huizing M, Ruitenbeek W, Thinnes FP, DePinto V, Wendel U, Trijbels FJ, Smit LM, ter Laak HJ, van den Heuvel LP. Huizing M, et al. Among authors: van den heuvel lp. Pediatr Res. 1996 May;39(5):760-5. doi: 10.1203/00006450-199605000-00003. Pediatr Res. 1996. PMID: 8726225 Free article.

4

Importance of mitochondrial transmembrane processes in human mitochondriopathies.

Huizing M, DePinto V, Ruitenbeek W, Trijbels FJ, van den Heuvel LP, Wendel U. Huizing M, et al. Among authors: van den heuvel lp. J Bioenerg Biomembr. 1996 Apr;28(2):109-14. doi: 10.1007/BF02110640. J Bioenerg Biomembr. 1996. PMID: 9132408 Review.

5

Human mitochondrial transmembrane metabolite carriers: tissue distribution and its implication for mitochondrial disorders.

Huizing M, Ruitenbeek W, van den Heuvel LP, Dolce V, Iacobazzi V, Smeitink JA, Palmieri F, Trijbels JM. Huizing M, et al. Among authors: van den heuvel lp. J Bioenerg Biomembr. 1998 Jun;30(3):277-84. doi: 10.1023/a:1020501021222. J Bioenerg Biomembr. 1998. PMID: 9733094

6

Carnitine-acylcarnitine carrier deficiency: identification of the molecular defect in a patient.

Huizing M, Wendel U, Ruitenbeek W, Iacobazzi V, IJlst L, Veenhuizen P, Savelkoul P, van den Heuvel LP, Smeitink JA, Wanders RJ, Trijbels JM, Palmieri F. Huizing M, et al. Among authors: van den heuvel lp. J Inherit Metab Dis. 1998 Jun;21(3):262-7. doi: 10.1023/a:1005324323401. J Inherit Metab Dis. 1998. PMID: 9686371 No abstract available.

7

cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed.

Loeffen JL, Triepels RH, van den Heuvel LP, Schuelke M, Buskens CA, Smeets RJ, Trijbels JM, Smeitink JA. Loeffen JL, et al. Among authors: van den heuvel lp. Biochem Biophys Res Commun. 1998 Dec 18;253(2):415-22. doi: 10.1006/bbrc.1998.9786. Biochem Biophys Res Commun. 1998. PMID: 9878551

8

SURFEIT-1 gene analysis and two-dimensional blue native gel electrophoresis in cytochrome c oxidase deficiency.

Coenen MJ, van den Heuvel LP, Nijtmans LG, Morava E, Marquardt I, Girschick HJ, Trijbels FJ, Grivell LA, Smeitink JA. Coenen MJ, et al. Among authors: van den heuvel lp. Biochem Biophys Res Commun. 1999 Nov 19;265(2):339-44. doi: 10.1006/bbrc.1999.1662. Biochem Biophys Res Commun. 1999. PMID: 10558868

9

Identification of four novel mutations in severe methylenetetrahydrofolate reductase deficiency.

Kluijtmans LA, Wendel U, Stevens EM, van den Heuvel LP, Trijbels FJ, Blom HJ. Kluijtmans LA, et al. Among authors: van den heuvel lp. Eur J Hum Genet. 1998 May-Jun;6(3):257-65. doi: 10.1038/sj.ejhg.5200182. Eur J Hum Genet. 1998. PMID: 9781030

10

Genetic characteristics of myoadenylate deaminase deficiency.

Verzijl HT, van Engelen BG, Luyten JA, Steenbergen GC, van den Heuvel LP, ter Laak HJ, Padberg GW, Wevers RA. Verzijl HT, et al. Among authors: van engelen bg, van den heuvel lp. Ann Neurol. 1998 Jul;44(1):140-3. doi: 10.1002/ana.410440124. Ann Neurol. 1998. PMID: 9667605 Clinical Trial.

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