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Journal of Neuroendocrinology|October 1, 1993
Role of CRH in glucopenia-induced adrenomedullary activation in ratsD S Goldstein, M Garty, G Bagdy, et al.
The Journal of Clinical Investigation|March 1, 1995
Decreased stress responsivity of central and peripheral catecholaminergic systems in aged 344/N Fischer ratsG Cizza, K Pacak, R Kvetnansky, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|August 14, 2021
A multigenomic liquid biopsy biomarker for neuroendocrine tumor disease outperforms CgA and has surgical and clinical utilityI M Modlin, M Kidd, M Falconi, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|March 23, 2012
Genetic screening for von Hippel-Lindau gene mutations in non-syndromic pheochromocytoma: low prevalence and false-positives or misdiagnosis indicate a need for cautionG Eisenhofer, C D Vocke, A Elkahloun, et al.
Molecular and Cellular Endocrinology|December 27, 2012
Anti-tumor effects of peptide analogs targeting neuropeptide hormone receptors on mouse pheochromocytoma cellsC G Ziegler, M Ullrich, A V Schally, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2001
Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypesG Eisenhofer, M M Walther, T T Huynh, et al.
Clinical Genetics|April 25, 2009
Penetrance and clinical consequences of a gross SDHB deletion in a large familyD C Solis, N Burnichon, H J L M Timmers, et al.
Endocrine-Related Cancer|October 1, 2008
Metastases but not cardiovascular mortality reduces life expectancy following surgical resection of apparently benign pheochromocytomaH J L M Timmers, F M Brouwers, A R M M Hermus, et al.
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