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92 results

Normal rates of whole-body fat oxidation and gluconeogenesis after overnight fasting and moderate-intensity exercise in patients with medium-chain acyl-CoA dehydrogenase deficiency.

Huidekoper HH, Ackermans MT, Koopman R, van Loon LJ, Sauerwein HP, Wijburg FA

Journal of inherited metabolic disease, 2013 Sep

doi: 10.1007/s10545-012-9532-8

Extended metabolic evaluation of suspected symptomatic hypoglycemia: the prolonged fast and beyond.

Soeters MR, Huidekoper HH, Duran M, Ackermans MT, Endert E, Fliers E, Wijburg FA, Wanders RJ, Sauerwein HP, Serlie MJ

Metabolism: clinical and experimental, 2010 Nov

doi: 10.1016/j.metabol.2010.01.024

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 HH, Visser G, Ackermans MT, Sauerwein HP, Wijburg FA

Journal of inherited metabolic disease, 2010 Feb

doi: 10.1007/s10545-009-9030-9

Fasting adaptation in idiopathic ketotic hypoglycemia: a mismatch between glucose production and demand.

Huidekoper HH, Duran M, Turkenburg M, Ackermans MT, Sauerwein HP, Wijburg FA

European journal of pediatrics, 2008 Aug

NCBI: 17934759

Prolonged moderate-intensity exercise without and with L-carnitine supplementation in patients with MCAD deficiency.

Huidekoper HH, Schneider J, Westphal T, Vaz FM, Duran M, Wijburg FA

Journal of inherited metabolic disease, 2006 Oct

NCBI: 16972171

OTX1 and OTX2 expression correlates with the clinicopathologic classification of medulloblastomas.

de Haas T, Oussoren E, Grajkowska W, Perek-Polnik M, Popovic M, Zadravec-Zaletel L, Perera M, Corte G, Wirths O, van Sluis P, Pietsch T, Troost D, Baas F, Versteeg R, Kool M

Journal of neuropathology and experimental neurology, 2006 Feb

NCBI: 16462208

Short-term exogenous galactose supplementation does not influence rate of appearance of galactose in patients with classical galactosemia.

Huidekoper HH, Bosch AM, van der Crabben SN, Sauerwein HP, Ackermans MT, Wijburg FA

Molecular genetics and metabolism, 2005 Mar

NCBI: 15694176

Deletions spanning the neurofibromatosis type 1 gene: implications for genotype-phenotype correlations in neurofibromatosis type 1?

Cnossen MH, van der Est MN, Breuning MH, van Asperen CJ, Breslau-Siderius EJ, van der Ploeg AT, de Goede-Bolder A, van den Ouweland AM, Halley DJ, Niermeijer MF

Human mutation, 1997

NCBI: 9143927