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Psychoneuroendocrinology|February 8, 2005
The combined T3/TRH test in depressed patients and healthy controlsCornelius Schüle, Thomas C Baghai, Vassiliki Tsikolata, et al.The Journal of Clinical Endocrinology and Metabolism|July 30, 2010
Novel activating mutations of the calcium-sensing receptor: the calcilytic NPS-2143 mitigates excessive signal transduction of mutant receptorsSaskia Letz, Ramona Rus, Christine Haag, et al.Clinical Chemistry and Laboratory Medicine|February 23, 2019
Calcitonin measurement in pediatrics: reference ranges are gender-dependent, validation in medullary thyroid cancer and thyroid diseasesFelix Eckelt, Mandy Vogel, Mandy Geserick, et al.Thyroid : Official Journal of the American Thyroid Association|September 6, 2012
Prevalence and clinical spectrum of nonsecretory medullary thyroid carcinoma in a series of 839 patients with sporadic medullary thyroid carcinomaKarin Frank-Raue, Andreas Machens, Gudrun Leidig-Bruckner, et al.Journal of Psychiatric Research|March 12, 2002
Nocturnal secretion of TSH and ACTH in male patients with depression and healthy controlsChristian Peteranderl, Irina A Antonijevic, Axel Steiger, et al.European Journal of Endocrinology|March 7, 2008
Characterization of the RET protooncogene transmembrane domain mutation S649L associated with nonaggressive medullary thyroid carcinomaMario Colombo-Benkmann, Zhenpeng Li, Burkhard Riemann, et al.Clinical Endocrinology|November 7, 2021
Medullary thyroid cancer with ectopic Cushing's syndrome: A multicentre case seriesViktoria F Koehler, Carmina T Fuss, Christina M Berr, et al.European Archives of Psychiatry and Clinical Neuroscience|March 5, 2005
The influence of 4-week treatment with sertraline on the combined T3/TRH test in depressed patientsCornelius Schüle, Thomas C Baghai, Lejla Alajbegovic, et al.The New England Journal of Medicine|October 17, 2003
Early malignant progression of hereditary medullary thyroid cancerAndreas Machens, Patricia Niccoli-Sire, Josef Hoegel, et al.Clinical Endocrinology|June 8, 2011
Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German surveyFriedhelm Raue, Josef Pichl, Helmuth-G Dörr, et al.Pageof 8