De Vries M - Search Results

1

Dietary intervention and oxidative phosphorylation capacity.

Morava E, Rodenburg R, van Essen HZ, De Vries M, Smeitink J. Morava E, et al. Among authors: de vries m. J Inherit Metab Dis. 2006 Aug;29(4):589. doi: 10.1007/s10545-006-0227-x. Epub 2006 Jun 19. J Inherit Metab Dis. 2006. PMID: 16786255

2

The intake of total protein, natural protein and protein substitute and growth of height and head circumference in Dutch infants with phenylketonuria.

Hoeksma M, Van Rijn M, Verkerk PH, Bosch AM, Mulder MF, de Klerk JB, de Koning TJ, Rubio-Gozalbo E, de Vries M, Sauer PJ, van Spronsen FJ. Hoeksma M, et al. Among authors: de klerk jb, de vries m, de koning tj. J Inherit Metab Dis. 2005;28(6):845-54. doi: 10.1007/s10545-005-0122-x. J Inherit Metab Dis. 2005. PMID: 16435176

3

Clinical and biochemical characteristics in patients with a high mutant load of the mitochondrial T8993G/C mutations.

Morava E, Rodenburg RJ, Hol F, de Vries M, Janssen A, van den Heuvel L, Nijtmans L, Smeitink J. Morava E, et al. Among authors: de vries m. Am J Med Genet A. 2006 Apr 15;140(8):863-8. doi: 10.1002/ajmg.a.31194. Am J Med Genet A. 2006. PMID: 16532470

4

Normal serum alanine concentration differentiates transient neonatal lactic acidemia from an inborn error of energy metabolism.

Morava E, Hogeveen M, De Vries M, Ruitenbeek W, de Boode WP, Smeitink J. Morava E, et al. Among authors: de boode wp, de vries m. Biol Neonate. 2006;90(3):207-9. doi: 10.1159/000093590. Epub 2006 May 29. Biol Neonate. 2006. PMID: 16733350

5

Multiple oxidative phosphorylation deficiencies in severe childhood multi-system disorders due to polymerase gamma (POLG1) mutations.

de Vries MC, Rodenburg RJ, Morava E, van Kaauwen EP, ter Laak H, Mullaart RA, Snoeck IN, van Hasselt PM, Harding P, van den Heuvel LP, Smeitink JA. de Vries MC, et al. Eur J Pediatr. 2007 Mar;166(3):229-34. doi: 10.1007/s00431-006-0234-9. Epub 2006 Sep 7. Eur J Pediatr. 2007. PMID: 16957900

6

Skeletal muscle ultrasonography in children with a dysfunction in the oxidative phosphorylation system.

Pillen S, Morava E, Van Keimpema M, Ter Laak HJ, De Vries MC, Rodenburg RJ, Zwarts MJ. Pillen S, et al. Among authors: de vries mc. Neuropediatrics. 2006 Jun;37(3):142-7. doi: 10.1055/s-2006-924512. Neuropediatrics. 2006. PMID: 16967365 Free article.

7

Mitochondrial disease criteria: diagnostic applications in children.

Morava E, van den Heuvel L, Hol F, de Vries MC, Hogeveen M, Rodenburg RJ, Smeitink JA. Morava E, et al. Among authors: de vries mc. Neurology. 2006 Nov 28;67(10):1823-6. doi: 10.1212/01.wnl.0000244435.27645.54. Neurology. 2006. PMID: 17130416

8

Resting muscle pain as the first clinical symptom in children carrying the MTTK A8344G mutation.

van de Glind G, de Vries M, Rodenburg R, Hol F, Smeitink J, Morava E. van de Glind G, et al. Among authors: de vries m. Eur J Paediatr Neurol. 2007 Jul;11(4):243-6. doi: 10.1016/j.ejpn.2007.01.004. Epub 2007 Feb 12. Eur J Paediatr Neurol. 2007. PMID: 17293137

9

Normal biochemical analysis of the oxidative phosphorylation (OXPHOS) system in a child with POLG mutations: a cautionary note.

de Vries MC, Rodenburg RJ, Morava E, Lammens M, van den Heuvel LP, Korenke GC, Smeitink JA. de Vries MC, et al. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S299-302. doi: 10.1007/s10545-008-0871-4. Epub 2008 May 20. J Inherit Metab Dis. 2008. PMID: 18500570

10

Major depression in adolescent children consecutively diagnosed with mitochondrial disorder.

Koene S, Kozicz TL, Rodenburg RJ, Verhaak CM, de Vries MC, Wortmann S, van de Heuvel L, Smeitink JA, Morava E. Koene S, et al. Among authors: de vries mc. J Affect Disord. 2009 Apr;114(1-3):327-32. doi: 10.1016/j.jad.2008.06.023. Epub 2008 Aug 9. J Affect Disord. 2009. PMID: 18692904

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