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Hormone Research|October 25, 2000
A novel nonsense mutation of the KAL gene in two brothers with Kallmann syndromeC Jansen, B I Hendriks-Stegeman, M Jansen
Blood|July 1, 1976
Identification of monocytes in suspensions of mononuclear cellsP H Rothbarth, I Hendriks-Sturkenboom, J S Ploem
Lung|January 1, 1992
Pulmonary function and resting breathing pattern in myotonic dystrophyJ M Bogaard, F G van der Meché, I Hendriks, et al.
Endocrinology|December 1, 1999
Insulin-like growth factor (IGF) II induced changes in expression of IGF binding proteins in lymphoid tissues of hIGF-II transgenic miceJ J Smink, J G Koster, B I Hendriks-Stegeman, et al.
European Journal of Endocrinology|January 10, 2004
A comparison of in vitro bioassays to determine cellular glucocorticoid sensitivityH Vermeer, B I Hendriks-Stegeman, A A Verrijn Stuart, et al.
The Journal of Clinical Endocrinology and Metabolism|January 10, 2003
Glucocorticoid-induced increase in lymphocytic FKBP51 messenger ribonucleic acid expression: a potential marker for glucocorticoid sensitivity, potency, and bioavailabilityHarry Vermeer, Brenda I Hendriks-Stegeman, Bart van der Burg, et al.
International Psychogeriatrics|December 19, 2018
How do people with dementia respond to different types of art? An explorative study into interactive museum programsI Hendriks, F J M Meiland, K Slotwinska, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the Pit1/POU1F1 geneB I Hendriks-Stegeman, K D Augustijn, B Bakker, et al.
Molecular and Cellular Endocrinology|May 8, 2004
An in vitro bioassay to determine individual sensitivity to glucocorticoids: induction of FKBP51 mRNA in peripheral blood mononuclear cellsHarry Vermeer, Brenda I Hendriks-Stegeman, Denise van Suylekom, et al.
Molecular Endocrinology (Baltimore, Md.)|February 22, 2007
Impaired peroxisome proliferator-activated receptor gamma function through mutation of a conserved salt bridge (R425C) in familial partial lipodystrophyEllen H Jeninga, Olivier van Beekum, Aalt D J van Dijk, et al.
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