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M I New

Showing results (131-140 of 292) with videos related to

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Clinical Nuclear Medicine|November 1, 1990
Bilateral adrenal uptake of gallium-67 citrate in a patient with congenital adrenal hyperplasiaM Lorberboym, S D Sarkar, P Speiser, et al.
The Journal of Pediatrics|April 1, 1972
Pseudohypopituitary dwarfism with normal plasma growth hormone and low serum sulfation factorM I New, E Schwartz, G A Parks, et al.
Recent Progress in Hormone Research|January 1, 1981
An update of congenital adrenal hyperplasiaM I New, B Dupont, S Pang, et al.
Psychoneuroendocrinology|January 1, 1995
Effects of early prenatal dexamethasone on the cognitive and behavioral development of young children: results of a pilot studyP D Trautman, H F Meyer-Bahlburg, J Postelnek, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1977
The interrelationship of sodium balance, plasma renin activity and ACTH in congenital adrenal hyperplasiaA Rösler, L S Levine, B Schneider, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1985
Excess mineralocorticoid receptor activity in patients with dexamethasone-suppressible hyperaldosteronism is under adrenocorticotropin controlP W Speiser, K O Martin, G Kao-Lo, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Prevalence of mild apparent mineralocorticoid excess in MennonitesF Ugrasbul, T Wiens, P Rubinstein, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Growth hormone therapy alone or in combination with gonadotropin-releasing hormone analog therapy to improve the height deficit in children with congenital adrenal hyperplasiaJ B Quintos, M G Vogiatzi, M D Harbison, et al.
Hormone Research|January 1, 1995
Failure of steroid replacement to consistently normalize pituitary function in congenital adrenal hyperplasia: hormonal and MRI dataP W Speiser, L Heier, J Serrat, et al.
Journal of Endocrinological Investigation|January 1, 1989
Growth and final height in classical and nonclassical 21-hydroxylase deficiencyM I New, J M Gertner, P W Speiser, et al.
Pageof 30

Showing results (131-140 of 292) with videos related to

Sort By:
Pageof 30
Clinical Nuclear Medicine|November 1, 1990
Bilateral adrenal uptake of gallium-67 citrate in a patient with congenital adrenal hyperplasiaM Lorberboym, S D Sarkar, P Speiser, et al.
The Journal of Pediatrics|April 1, 1972
Pseudohypopituitary dwarfism with normal plasma growth hormone and low serum sulfation factorM I New, E Schwartz, G A Parks, et al.
Recent Progress in Hormone Research|January 1, 1981
An update of congenital adrenal hyperplasiaM I New, B Dupont, S Pang, et al.
Psychoneuroendocrinology|January 1, 1995
Effects of early prenatal dexamethasone on the cognitive and behavioral development of young children: results of a pilot studyP D Trautman, H F Meyer-Bahlburg, J Postelnek, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1977
The interrelationship of sodium balance, plasma renin activity and ACTH in congenital adrenal hyperplasiaA Rösler, L S Levine, B Schneider, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1985
Excess mineralocorticoid receptor activity in patients with dexamethasone-suppressible hyperaldosteronism is under adrenocorticotropin controlP W Speiser, K O Martin, G Kao-Lo, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Prevalence of mild apparent mineralocorticoid excess in MennonitesF Ugrasbul, T Wiens, P Rubinstein, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Growth hormone therapy alone or in combination with gonadotropin-releasing hormone analog therapy to improve the height deficit in children with congenital adrenal hyperplasiaJ B Quintos, M G Vogiatzi, M D Harbison, et al.
Hormone Research|January 1, 1995
Failure of steroid replacement to consistently normalize pituitary function in congenital adrenal hyperplasia: hormonal and MRI dataP W Speiser, L Heier, J Serrat, et al.
Journal of Endocrinological Investigation|January 1, 1989
Growth and final height in classical and nonclassical 21-hydroxylase deficiencyM I New, J M Gertner, P W Speiser, et al.
Pageof 30