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B Grossman

Showing results (501-510 of 794) with videos related to

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Clinical Endocrinology|January 17, 2004
Successful treatment of childhood-onset Cushing's disease is associated with persistent reduction in growth hormone secretionP V Carroll, J P Monson, A B Grossman, et al.
Hormone Research|September 30, 2005
Efficient short-term control of hypercortisolaemia by low-dose etomidate in severe paediatric Cushing's diseaseJ E Greening, C E Brain, L A Perry, et al.
Journal of Neuroendocrinology|August 12, 1999
The effect of growth hormone secretagogues and neuropeptide Y on hypothalamic hormone release from acute rat hypothalamic explantsM Korbonits, J A Little, M L Forsling, et al.
British Journal of Anaesthesia|June 12, 1999
Dissociation of pituitary-adrenal and catecholamine activation after induced cardiac arrest and defibrillationM J O'Leary, A C Timmins, J N Appleby, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2001
The expression of the growth hormone secretagogue receptor ligand ghrelin in normal and abnormal human pituitary and other neuroendocrine tumorsM Korbonits, S A Bustin, M Kojima, et al.
Nuclear Medicine Communications|March 4, 2003
123I-Interleukin-2: biochemical characterization and in vivo use for imaging autoimmune diseasesA Signore, A Picarelli, A Annovazzi, et al.
European Journal of Endocrinology|November 1, 1996
L-arginine is unlikely to exert neuroendocrine effects in humans via the generation of nitric oxideM Korbonits, P J Trainer, G Fanciulli, et al.
Clinical Endocrinology|January 5, 2007
Unmasking of central hypothyroidism following growth hormone replacement in adult hypopituitary patientsAmar Agha, Dorothy Walker, Les Perry, et al.
The Journal of Clinical Endocrinology and Metabolism|February 3, 2005
Fasting and postprandial hyperghrelinemia in Prader-Willi syndrome is partially explained by hypoinsulinemia, and is not due to peptide YY3-36 deficiency or seen in hypothalamic obesity due to craniopharyngiomaAnthony P Goldstone, Michael Patterson, Nila Kalingag, et al.
Clinical Endocrinology|December 1, 1996
Differential stimulation of cortisol and dehydroepiandrosterone levels by food in obese and normal subjects: relation to body fat distributionM Korbonits, P J Trainer, M L Nelson, et al.
Pageof 80

Showing results (501-510 of 794) with videos related to

Sort By:
Pageof 80
Clinical Endocrinology|January 17, 2004
Successful treatment of childhood-onset Cushing's disease is associated with persistent reduction in growth hormone secretionP V Carroll, J P Monson, A B Grossman, et al.
Hormone Research|September 30, 2005
Efficient short-term control of hypercortisolaemia by low-dose etomidate in severe paediatric Cushing's diseaseJ E Greening, C E Brain, L A Perry, et al.
Journal of Neuroendocrinology|August 12, 1999
The effect of growth hormone secretagogues and neuropeptide Y on hypothalamic hormone release from acute rat hypothalamic explantsM Korbonits, J A Little, M L Forsling, et al.
British Journal of Anaesthesia|June 12, 1999
Dissociation of pituitary-adrenal and catecholamine activation after induced cardiac arrest and defibrillationM J O'Leary, A C Timmins, J N Appleby, et al.
The Journal of Clinical Endocrinology and Metabolism|February 7, 2001
The expression of the growth hormone secretagogue receptor ligand ghrelin in normal and abnormal human pituitary and other neuroendocrine tumorsM Korbonits, S A Bustin, M Kojima, et al.
Nuclear Medicine Communications|March 4, 2003
123I-Interleukin-2: biochemical characterization and in vivo use for imaging autoimmune diseasesA Signore, A Picarelli, A Annovazzi, et al.
European Journal of Endocrinology|November 1, 1996
L-arginine is unlikely to exert neuroendocrine effects in humans via the generation of nitric oxideM Korbonits, P J Trainer, G Fanciulli, et al.
Clinical Endocrinology|January 5, 2007
Unmasking of central hypothyroidism following growth hormone replacement in adult hypopituitary patientsAmar Agha, Dorothy Walker, Les Perry, et al.
The Journal of Clinical Endocrinology and Metabolism|February 3, 2005
Fasting and postprandial hyperghrelinemia in Prader-Willi syndrome is partially explained by hypoinsulinemia, and is not due to peptide YY3-36 deficiency or seen in hypothalamic obesity due to craniopharyngiomaAnthony P Goldstone, Michael Patterson, Nila Kalingag, et al.
Clinical Endocrinology|December 1, 1996
Differential stimulation of cortisol and dehydroepiandrosterone levels by food in obese and normal subjects: relation to body fat distributionM Korbonits, P J Trainer, M L Nelson, et al.
Pageof 80