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Effect of i.v. amino acids on satiety in humans.
Published in:
1999
By:
- Gielkens HAJ;
- Penning C;
- van dan Biggelaar A;
- Onkenhout W;
- Lamers CBH;
- Masclee AAM;
- Gielkens, H A;
- Penning, C;
- van dan Biggelaar, A;
- Onkenhout, W;
- Lamers, C B;
- Masclee, A A
Publication type:
journal article
Intermediates of unsaturated fatty acid oxidation are incorporated in triglycerides but not in phospholipids in tissues from patients with mitochondrial β-oxidation defects.
Published in:
Journal of Inherited Metabolic Disease, 2001, v. 24, n. 3, p. 337, doi. 10.1023/A:1010592232317
By:
- Onkenhout, W.;
- Venizelos, V.;
- Scholte, H.;
- de Klerk, J.;
- Poorthuis, B.
Publication type:
Article
Pyridoxine-responsive nephrocalcinosis and glycolic aciduria in two siblings without hyperoxaluria and with normal alanine:glyoxalate aminotransferase activity.
Published in:
Journal of Inherited Metabolic Disease, 2000, v. 23, n. 1, p. 91, doi. 10.1023/A:1005615417126
By:
- Kist-van Holthe, J.;
- Onkenhout, W.;
- van der Heijden, A.
Publication type:
Article
Adenylosuccinase deficiency presenting with epilepsy in early infancy.
Published in:
Journal of Inherited Metabolic Disease, 1997, v. 20, n. 4, p. 606, doi. 10.1023/A:1005323512982
By:
- Maaswinkel-Mooij, P.D.;
- Laan, L.;
- Onkenhout, W.;
- Brouwer, O.;
- Jaeken, J.;
- Poorthuis, B.
Publication type:
Article
Impaired homocysteine metabolism: A risk factor in young adults with atherosclerotic arterial occlusive disease of the leg.
Published in:
British Journal of Surgery, 1994, v. 81, n. 8, p. 1114, doi. 10.1002/bjs.1800810811
By:
- Aronson, D. C.;
- Onkenhout, W.;
- Raben, A. M. T. J.;
- Oudenhoven, L. F. I. J.;
- Brommer, E. J. P.;
- van Bockel, J. H.
Publication type:
Article
Cystathionine Levels in Patients With Huntington Disease.
Published in:
PLoS Currents, 2015, p. 162, doi. 10.1371/currents.hd.c63b441d04bb6738c0234f91c2b3e312
By:
- Aziz, N. A.;
- Onkenhout, W.;
- Kerstens, H. J.;
- Roos, Raymund A. C.
Publication type:
Article
Polyhydramnios and cerebellar atrophy: a prenatal presentation of mitochondrial encephalomyopathy caused by mutations in the FBXL4 gene.
Published in:
Clinical Case Reports, 2016, v. 4, n. 4, p. 425, doi. 10.1002/ccr3.511
By:
- Rij, Maartje C.;
- Jansen, Fenna A. R.;
- Hellebrekers, Debby M. E. I.;
- Onkenhout, W.;
- Smeets, Hubert J. M.;
- Hendrickx, Alexandra T.;
- Gottschalk, Ralph W. H.;
- Steggerda, Sylke J.;
- Peeters‐Scholte, Cacha M. P. C. D.;
- Haak, Monique C.;
- Hilhorst‐Hofstee, Yvonne
Publication type:
Article
Fibroblast growth factor 21 as a biomarker for long‐term complications in organic acidemias.
Published in:
Journal of Inherited Metabolic Disease, 2018, v. 41, n. 6, p. 1179, doi. 10.1007/s10545-018-0244-6
By:
- Molema, F.;
- Jacobs, E. H.;
- Onkenhout, W.;
- Schoonderwoerd, G. C.;
- Langendonk, J. G.;
- Williams, Monique
Publication type:
Article
Fibroblast growth factor 21 as a biomarker for long-term complications in organic acidemias.
Published in:
Journal of Inherited Metabolic Disease, 2018, v. 41, n. 6, p. 1179, doi. 10.1007/s10545-018-0244-6
By:
- Molema, F.;
- Jacobs, E. H.;
- Onkenhout, W.;
- Schoonderwoerd, G. C.;
- Langendonk, J. G.;
- Williams, Monique
Publication type:
Article
GLUT-1 deficiency without epilepsy—an exceptional case.
Published in:
Journal of Inherited Metabolic Disease, 2003, v. 26, n. 6, p. 559, doi. 10.1023/A:1025999914822
By:
- Overweg-Plandsoen, W.;
- Groener, J.;
- Wang, D.;
- Onkenhout, W.;
- Brouwer, O.;
- Bakker, H.;
- De Vivo, D.
Publication type:
Article
Psychological and metabolic responses of carbohydrate craving obese patients to carbohydrate, fat and protein-rich meals.
Published in:
International Journal of Obesity & Related Metabolic Disorders, 1997, v. 21, n. 10, p. 860, doi. 10.1038/sj.ijo.0800470
By:
- Toornvliet, A C;
- Pijl, H;
- Tuinenburg, J C;
- Wever, BM Elte-de;
- Pieters, M S M;
- Frölich, M;
- Onkenhout, W;
- Meinders, A E
Publication type:
Article
Mental retardation and behavioral problems as presenting signs of a creatine synthesis defect.
Published in:
2000
By:
- Van Der Knaap, Marjo S.;
- Verhoeven, Nanda M.;
- Maaswinkel-Mooij, Petra;
- Pouwels, Petra J. W.;
- Onkenhout, Wim;
- Peeters, Els A. J.;
- Stöckler-Ipsiroglu, Sylvia;
- Jakobs, Cornelius;
- van der Knaap, M S;
- Verhoeven, N M;
- Maaswinkel-Mooij, P;
- Pouwels, P J;
- Onkenhout, W;
- Peeters, E A;
- Stöckler-Ipsiroglu, S;
- Jakobs, C
Publication type:
journal article
Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset.
Published in:
Annals of Neurology, 1998, v. 43, n. 4, p. 540, doi. 10.1002/ana.410430422
By:
- Smelt, A. H. M.;
- Poorthuis, B. J. H. M.;
- Onkenhout, W.;
- Scholte, H. R.;
- Andresen, B. S.;
- van Duinen, S. G.;
- Gregersen, N.;
- Wintzen, A. R.
Publication type:
Article

Found: 13