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Hormone Research
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January 1, 1993
Results of long-term therapy with growth hormone in two dose regimens in Turner syndrome. Dutch Growth Hormone Working Group
H 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 puberty
F 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 defects
S 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 approach
R 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 activation
D 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 diseases
E 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 osteopenia
F 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 gene
H 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 protein
H 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 Management
S D Joustra, C A Heinen, N Schoenmakers, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 78) with videos related to
Sort By:
Page
of 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 Group
H 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 puberty
F 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 defects
S 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 approach
R 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 activation
D 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 diseases
E 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 osteopenia
F 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 gene
H 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 protein
H 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 Management
S D Joustra, C A Heinen, N Schoenmakers, et al.
Page
of 8