Onkenhout W - Search Results

1

Mental retardation and behavioral problems as presenting signs of a creatine synthesis defect.

van der Knaap MS, Verhoeven NM, Maaswinkel-Mooij P, Pouwels PJ, Onkenhout W, Peeters EA, Stöckler-Ipsiroglu S, Jakobs C. van der Knaap MS, et al. Among authors: onkenhout w. Ann Neurol. 2000 Apr;47(4):540-3. doi: 10.1002/1531-8249(200004)47:4<540::aid-ana23>3.3.co;2-b. Ann Neurol. 2000. PMID: 10762171

2

4-Hydroxybutyric aciduria: further clinical heterogeneity in a new case.

Onkenhout W, Maaswinkel-Mooij PD, Poorthuis BJ. Onkenhout W, et al. Eur J Pediatr. 1989 Dec;149(3):194-6. doi: 10.1007/BF01958280. Eur J Pediatr. 1989. PMID: 2482184

3

Adenylosuccinase deficiency presenting with epilepsy in early infancy.

Maaswinkel-Mooij PD, Laan LA, Onkenhout W, Brouwer OF, Jaeken J, Poorthuis BJ. Maaswinkel-Mooij PD, et al. Among authors: onkenhout w. J Inherit Metab Dis. 1997 Aug;20(4):606-7. doi: 10.1023/a:1005323512982. J Inherit Metab Dis. 1997. PMID: 9266401 No abstract available.

4

L-Arabinosuria: a new defect in human pentose metabolism.

Onkenhout W, Groener JE, Verhoeven NM, Yin C, Laan LA. Onkenhout W, et al. Mol Genet Metab. 2002 Sep-Oct;77(1-2):80-5. doi: 10.1016/s1096-7192(02)00125-7. Mol Genet Metab. 2002. PMID: 12359133

5

Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia.

Maaswinkel-Mooij PD, Van den Bogert C, Scholte HR, Onkenhout W, Brederoo P, Poorthuis BJ. Maaswinkel-Mooij PD, et al. Among authors: onkenhout w. J Pediatr. 1996 May;128(5 Pt 1):679-83. doi: 10.1016/s0022-3476(96)80134-x. J Pediatr. 1996. PMID: 8627441

6

Comments on 'Infantile hypophosphatasia without bone deformities presenting with severe pyridoxine-resistant seizures' in Molecular Genetics and Metabolism' 2014 Mar;111(3):404-7 by M.G. de Roo, N.G. Abeling, C.B. Majoie, A.M. Bosch, J.H. Koelman, J.M. Cobben, M. Duran, B.T. Poll-The.

van der Stoep N, Onkenhout W, Prins S, Struys E, Jakobs C, Peeters-Scholte C. van der Stoep N, et al. Among authors: onkenhout w. Mol Genet Metab Rep. 2014 May 10;1:220-222. doi: 10.1016/j.ymgmr.2014.04.005. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896090 Free PMC article. No abstract available.

7

Adult adrenoleukodystrophy: the clinical spectrum in a large Dutch family.

Zwetsloot CP, Padberg GW, van Seters AP, Maaswinkel-Mooy PD, Onkenhout W. Zwetsloot CP, et al. Among authors: onkenhout w. J Neurol. 1992 Feb;239(2):107-11. doi: 10.1007/BF00862985. J Neurol. 1992. PMID: 1313076

8

Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset.

Smelt AH, Poorthuis BJ, Onkenhout W, Scholte HR, Andresen BS, van Duinen SG, Gregersen N, Wintzen AR. Smelt AH, et al. Among authors: onkenhout w. Ann Neurol. 1998 Apr;43(4):540-4. doi: 10.1002/ana.410430422. Ann Neurol. 1998. PMID: 9546340

9

Increased neurotoxicity of arsenic in methylenetetrahydrofolate reductase deficiency.

Brouwer OF, Onkenhout W, Edelbroek PM, de Kom JF, de Wolff FA, Peters AC. Brouwer OF, et al. Among authors: onkenhout w. Clin Neurol Neurosurg. 1992;94(4):307-10. doi: 10.1016/0303-8467(92)90179-7. Clin Neurol Neurosurg. 1992. PMID: 1335858

10

GLUT-1 deficiency without epilepsy--an exceptional case.

Overweg-Plandsoen WC, Groener JE, Wang D, Onkenhout W, Brouwer OF, Bakker HD, De Vivo DC. Overweg-Plandsoen WC, et al. Among authors: onkenhout w. J Inherit Metab Dis. 2003;26(6):559-63. doi: 10.1023/a:1025999914822. J Inherit Metab Dis. 2003. PMID: 14605501

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

50 results

Search Page