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W Oostdijk

Showing results (61-70 of 78) with videos related to

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Hormone Research|January 1, 1993
Results of long-term therapy with growth hormone in two dose regimens in Turner syndrome. Dutch Growth Hormone Working GroupH E Nienhuis, C Rongen-Westerlaken, J M Wit, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2001
Management of puberty in constitutional delay of growth and pubertyF De Luca, J Argente, L Cavallo, et al.
European Journal of Endocrinology|August 13, 2015
The growth response to GH treatment is greater in patients with SHOX enhancer deletions compared to SHOX defectsS H Donze, C R Meijer, S G Kant, et al.
Hormone Research in Paediatrics|June 6, 2013
Pharmacokinetics and pharmacodynamics of orally administered clonidine: a model-based approachR H Klein, R Alvarez-Jimenez, R N Sukhai, et al.
European Journal of Endocrinology|January 5, 2012
A mosaic de novo duplication of 17q21-25 is associated with GH insensitivity, disturbed in vitro CD28-mediated signaling, and decreased STAT5B, PI3K, and NF-κB activationD Mul, S Wu, R A de Paus, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 1, 1996
Screening for coeliac disease in Dutch children with associated diseasesE K George, M L Mearin, J Bouquet, et al.
Archives of Disease in Childhood|October 15, 2005
Growth hormone treatment in children with rheumatic disease, corticosteroid induced growth retardation, and osteopeniaF K Grote, L W A Van Suijlekom-Smit, D Mul, et al.
The Journal of Clinical Endocrinology and Metabolism|July 30, 2010
Short stature associated with a novel heterozygous mutation in the insulin-like growth factor 1 geneH A van Duyvenvoorde, P A van Setten, M J E Walenkamp, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|January 18, 2011
The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated proteinH A van Duyvenvoorde, J van Doorn, J Koenig, et al.
The Journal of Clinical Endocrinology and Metabolism|February 4, 2016
IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical ManagementS D Joustra, C A Heinen, N Schoenmakers, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Hormone Research|January 1, 1993
Results of long-term therapy with growth hormone in two dose regimens in Turner syndrome. Dutch Growth Hormone Working GroupH E Nienhuis, C Rongen-Westerlaken, J M Wit, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2001
Management of puberty in constitutional delay of growth and pubertyF De Luca, J Argente, L Cavallo, et al.
European Journal of Endocrinology|August 13, 2015
The growth response to GH treatment is greater in patients with SHOX enhancer deletions compared to SHOX defectsS H Donze, C R Meijer, S G Kant, et al.
Hormone Research in Paediatrics|June 6, 2013
Pharmacokinetics and pharmacodynamics of orally administered clonidine: a model-based approachR H Klein, R Alvarez-Jimenez, R N Sukhai, et al.
European Journal of Endocrinology|January 5, 2012
A mosaic de novo duplication of 17q21-25 is associated with GH insensitivity, disturbed in vitro CD28-mediated signaling, and decreased STAT5B, PI3K, and NF-κB activationD Mul, S Wu, R A de Paus, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 1, 1996
Screening for coeliac disease in Dutch children with associated diseasesE K George, M L Mearin, J Bouquet, et al.
Archives of Disease in Childhood|October 15, 2005
Growth hormone treatment in children with rheumatic disease, corticosteroid induced growth retardation, and osteopeniaF K Grote, L W A Van Suijlekom-Smit, D Mul, et al.
The Journal of Clinical Endocrinology and Metabolism|July 30, 2010
Short stature associated with a novel heterozygous mutation in the insulin-like growth factor 1 geneH A van Duyvenvoorde, P A van Setten, M J E Walenkamp, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|January 18, 2011
The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated proteinH A van Duyvenvoorde, J van Doorn, J Koenig, et al.
The Journal of Clinical Endocrinology and Metabolism|February 4, 2016
IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical ManagementS D Joustra, C A Heinen, N Schoenmakers, et al.
Pageof 8