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The Journal of Clinical Endocrinology and Metabolism|February 1, 1996
Fasting as a metabolic stress paradigm selectively amplifies cortisol secretory burst mass and delays the time of maximal nyctohemeral cortisol concentrations in healthy menM Bergendahl, M L Vance, A Iranmanesh, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1989
Octreotide suppresses both growth hormone (GH) and GH-releasing hormone (GHRH) in acromegaly due to ectopic GHRH secretionD E Moller, A C Moses, K Jones, et al.
Pituitary|June 1, 2001
Double pituitary lesions in three patients with Cushing's diseaseB P Meij, M B Lopes, M L Vance, et al.
Neuroscience and Biobehavioral Reviews|January 1, 1995
Neuroendocrine regulation of growth hormone secretionM O Thorner, M L Hartman, M L Vance, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1993
Amplitude suppression of the pulsatile mode of immunoradiometric luteinizing hormone release in fasting-induced hypoandrogenemia in normal menJ D Veldhuis, A Iranmanesh, W S Evans, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1987
Role of dopamine in the regulation of growth hormone secretion: dopamine and bromocriptine augment growth hormone (GH)-releasing hormone-stimulated GH secretion in normal manM L Vance, D L Kaiser, L A Frohman, et al.
Acta Paediatrica Scandinavica. Supplement|January 1, 1988
Contemporary tools for the analysis of episodic growth hormone secretion and clearance in vivoJ D Veldhuis, A Faria, M L Vance, et al.
The American Journal of Physiology|January 1, 1991
Temporal structure of in vivo growth hormone secretory events in humansM L Hartman, A C Faria, M L Vance, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1990
Somatotropin pulse frequency and basal concentrations are increased in acromegaly and are reduced by successful therapyM L Hartman, J D Veldhuis, M L Vance, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1989
Lack of in vivo somatotroph desensitization or depletion after 14 days of continuous growth hormone (GH)-releasing hormone administration in normal men and a GH-deficient boyM L Vance, D L Kaiser, P M Martha, et al.
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