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Clinical Endocrinology
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March 1, 1993
Blood pressure and the renin-angiotensin-aldosterone system in children receiving recombinant human growth hormone
J S Barton, P C Hindmarsh, M A Preece, et al.
Clinical Endocrinology
|
November 3, 1998
Gonadotrophin pulsatility in girls with the Turner syndrome: modulation by exogenous sex steroids
N C Nathwani, P C Hindmarsh, A A Massarano, et al.
Nature Genetics
|
June 16, 1999
A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans
J C Achermann, M Ito, M Ito, et al.
Hormone Research
|
May 15, 2002
17-Hydroxylase/17,20 lyase deficiency diagnosed during childhood
O D Wolthers, G Rumsby, K Techatraisak, et al.
Acta Endocrinologica
|
March 1, 1990
Growth hormone increases rate of pubertal maturation
F Darendeliler, P C Hindmarsh, M A Preece, et al.
Pediatric Research
|
December 1, 1995
Isolated growth hormone deficiency: testing the little mouse hypothesis in man and exclusion of mutations within the extracellular domain of the growth hormone-releasing hormone receptor
Y Cao, J K Wagner, P C Hindmarsh, et al.
Clinical Endocrinology
|
September 1, 1999
Ontogeny of serum leptin concentrations in the human
M Geary, R Herschkovitz, P J Pringle, et al.
Pediatric Research
|
October 6, 1999
Treatment of achondroplasia with growth hormone: six years of experience
U Ramaswami, G Rumsby, H A Spoudeas, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 16, 2001
Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: is current replacement therapy satisfactory?
E Charmandari, D R Matthews, A Johnston, et al.
The Journal of Endocrinology
|
September 1, 1991
The use of low doses of ACTH in the investigation of adrenal function in man
S Crowley, P C Hindmarsh, P Holownia, et al.
Page
of 20
Search research articles
Search
Showing results (101-110 of 194) with videos related to
Sort By:
Page
of 20
Clinical Endocrinology
|
March 1, 1993
Blood pressure and the renin-angiotensin-aldosterone system in children receiving recombinant human growth hormone
J S Barton, P C Hindmarsh, M A Preece, et al.
Clinical Endocrinology
|
November 3, 1998
Gonadotrophin pulsatility in girls with the Turner syndrome: modulation by exogenous sex steroids
N C Nathwani, P C Hindmarsh, A A Massarano, et al.
Nature Genetics
|
June 16, 1999
A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans
J C Achermann, M Ito, M Ito, et al.
Hormone Research
|
May 15, 2002
17-Hydroxylase/17,20 lyase deficiency diagnosed during childhood
O D Wolthers, G Rumsby, K Techatraisak, et al.
Acta Endocrinologica
|
March 1, 1990
Growth hormone increases rate of pubertal maturation
F Darendeliler, P C Hindmarsh, M A Preece, et al.
Pediatric Research
|
December 1, 1995
Isolated growth hormone deficiency: testing the little mouse hypothesis in man and exclusion of mutations within the extracellular domain of the growth hormone-releasing hormone receptor
Y Cao, J K Wagner, P C Hindmarsh, et al.
Clinical Endocrinology
|
September 1, 1999
Ontogeny of serum leptin concentrations in the human
M Geary, R Herschkovitz, P J Pringle, et al.
Pediatric Research
|
October 6, 1999
Treatment of achondroplasia with growth hormone: six years of experience
U Ramaswami, G Rumsby, H A Spoudeas, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 16, 2001
Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: is current replacement therapy satisfactory?
E Charmandari, D R Matthews, A Johnston, et al.
The Journal of Endocrinology
|
September 1, 1991
The use of low doses of ACTH in the investigation of adrenal function in man
S Crowley, P C Hindmarsh, P Holownia, et al.
Page
of 20