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J L Clark

Showing results (151-160 of 204) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|January 4, 2003
NESTEGG: aims and strategies. Northern European Study of Genes in GrowthLinda B Johnston, Linda Fryklund, Adrian J L Clark, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2005
The aberrant expression of the gastric inhibitory polypeptide (GIP) receptor in adrenal hyperplasia: does chronic adrenocorticotropin exposure stimulate up-regulation of GIP receptors in Cushing's disease?F M Swords, S Aylwin, L Perry, et al.
European Journal of Pediatrics|May 28, 2013
Familial glucocorticoid deficiency: a diagnostic challenge during acute illnessAbdelhadi M Habeb, Claire R Hughes, Rida Al-Arabi, et al.
The Journal of Clinical Endocrinology and Metabolism|April 24, 2008
A novel variant of familial glucocorticoid deficiency prevalent among the Irish Traveler populationStephen M P O'Riordan, Sally A Lynch, Peter C Hindmarsh, et al.
The Journal of Clinical Endocrinology and Metabolism|February 17, 2012
An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W)Serap Turan, Claire Hughes, Zeynep Atay, et al.
European Journal of Endocrinology|October 11, 2007
Idiopathic short stature: will genetics influence the choice between GH and IGF-I therapy?Martin O Savage, Cecilia Camacho-Hübner, Alessia David, et al.
Laboratory Animal Science|January 1, 1989
A standard procedure for measuring rodent bedding particle size and dust contentJ E Thigpen, E H Lebetkin, M L Dawes, et al.
Journal of Endocrinological Investigation|December 13, 2003
Rapid desensitisation of the GH secretagogue (ghrelin) receptor to hexarelin in vitroR D Orkin, D I New, D Norman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 9, 2005
Novel growth hormone receptor mutation in a Chinese patient with Laron syndromeHamilton N T Hui, Louise A Metherell, K L Ng, et al.
European Journal of Endocrinology|October 13, 2004
TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiencyL A Metherell, M O Savage, M Dattani, et al.
Pageof 21

Showing results (151-160 of 204) with videos related to

Sort By:
Pageof 21
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 4, 2003
NESTEGG: aims and strategies. Northern European Study of Genes in GrowthLinda B Johnston, Linda Fryklund, Adrian J L Clark, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2005
The aberrant expression of the gastric inhibitory polypeptide (GIP) receptor in adrenal hyperplasia: does chronic adrenocorticotropin exposure stimulate up-regulation of GIP receptors in Cushing's disease?F M Swords, S Aylwin, L Perry, et al.
European Journal of Pediatrics|May 28, 2013
Familial glucocorticoid deficiency: a diagnostic challenge during acute illnessAbdelhadi M Habeb, Claire R Hughes, Rida Al-Arabi, et al.
The Journal of Clinical Endocrinology and Metabolism|April 24, 2008
A novel variant of familial glucocorticoid deficiency prevalent among the Irish Traveler populationStephen M P O'Riordan, Sally A Lynch, Peter C Hindmarsh, et al.
The Journal of Clinical Endocrinology and Metabolism|February 17, 2012
An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W)Serap Turan, Claire Hughes, Zeynep Atay, et al.
European Journal of Endocrinology|October 11, 2007
Idiopathic short stature: will genetics influence the choice between GH and IGF-I therapy?Martin O Savage, Cecilia Camacho-Hübner, Alessia David, et al.
Laboratory Animal Science|January 1, 1989
A standard procedure for measuring rodent bedding particle size and dust contentJ E Thigpen, E H Lebetkin, M L Dawes, et al.
Journal of Endocrinological Investigation|December 13, 2003
Rapid desensitisation of the GH secretagogue (ghrelin) receptor to hexarelin in vitroR D Orkin, D I New, D Norman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 9, 2005
Novel growth hormone receptor mutation in a Chinese patient with Laron syndromeHamilton N T Hui, Louise A Metherell, K L Ng, et al.
European Journal of Endocrinology|October 13, 2004
TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiencyL A Metherell, M O Savage, M Dattani, et al.
Pageof 21