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prof. dr. B. (Gepke) Veneman

prof. dr. B. (Gepke) Veneman

Assistant Professor - medical

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Research Output (176)

Perioperative measures in very long chain acyl-CoA dehydrogenase deficiency.

Vellekoop P., Diekman E.F., van Tuijl I., de Vries M.M., van Hasselt P.M., Visser G. 2011, In: Molecular Genetics and Metabolism. 103 , p. 96-7 2 p.

Whole body composition analysis by the BodPod air-displacement plethysmography method in children with phenylketonuria shows a higher body fat percentage

Albersen Monique, Bonthuis Marjolein, de Roos Nicole M., van den Hurk TAM, Weber Ems Carbasius, Hendriks Margriet M. W. B., de Sain-van der Velden Monique G. M., de Koning Tom J., Visser Gepke Dec 2010, In: Journal of Inherited Metabolic Disease. 33 , p. S283-S288 6 p.

Mucopolysacharidose type I:De ziekten van Hurler en van Scheie

Teunissen Q. G.A., Van Spronsen F. J., Visser G., Brands M. M.M.G., Van Der Ploeg A. T., Wijburg F. A. 1 Jan 2010, In: Tijdschrift voor Kindergeneeskunde. 78 , p. 57-62 6 p.

A potential role for muscle in glucose homeostasis: in vivo kinetic studies in glycogen storage disease type 1a and fructose-1,6-bisphosphatase deficiency.

Huidekoper H.H., Visser G., Ackermans M.T., Sauerwein H.P., Wijburg F.A. 2010, In: Journal of Inherited Metabolic Disease. 33 , p. 25-31 7 p.

The clinical utility of MRI in patients with neurodevelopmental disorders of unknown origin

Engbers H.M., Nievelstein R.A.J., Gooskens R.H.J.M., Kroes H.Y., van Empelen R., Braams O.B., Wittebol-Post D., Hendriks M.M.W.B., Visser G. 2010, In: European Journal of Neurology. 17 , p. 815-822 8 p.

GAMT-deficiëntie: een behandelbare stoornis in de creatinestofwisseling

Dam B.J.G., Prinsen H.C.M.T., Hofstede F.C., Salomons G.S., Visser G. 2010, In: Tijdschrift voor Kindergeneeskunde. 78 , p. 209-212 4 p.

Exercise stress testing in children with metabolic or neuromuscular disorders

Takken Tim, Groen Wim G, Hulzebos Erik H, Ernsting Cornelia G, van Hasselt Peter M, Prinsen Berthil H, Helders Paul J, Visser Gepke 2010, In: International Journal of Pediatrics. 2010

Reply

Engbers Hannelie M., Berger Ruud, Ven Hasselt Peter, De Koning Tom, Monique G. M.de Sain van der Velden, Kroes Hester, Visser Gepke 1 Apr 2009, In: Annals of Neurology. 65 1 p.

Novel loci and candidate genes for autism spectrum disorder detected by SNP array based segmental aneuploidy screening

Poot M., Verbeek N.E., van ´t Slot R., Nelen M.R., van Daalen E., Ozgen H.M., Vorstman J.A.S., de Jonge M.V., Kroes H.Y., Terhal P.A., Beemer F.A., van der Smagt J.J., Ippel P.F., van den Boogaard M.J.H., van der Zwaag B., Visser G., Staal W.G., van Engeland H., Burbach J.P.H., Brilstra E.H., Freitag C.M., Ploos van Amstel H.K., Hochstenbach P.F.R. 9 Mar 2009,

Comment on: Metabolic evaluation in neurodevelopmental disabilities. Shevell M.

Engbers H.M., Berger R., van Hasselt P.M., de Koning T.J., de Sain - van der Velden M.G.M., Kroes H.Y., Visser G. 2009, In: Annals of Neurology. 65 , p. 483-484 2 p.

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