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European Journal of Endocrinology|April 2, 2016
'Incidental' and 'non-incidental' thyroid papillary microcarcinomas are two different entitiesMaria Annateresa Provenzale, Emilio Fiore, Clara Ugolini, et al.
European Journal of Endocrinology|July 13, 2016
From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP networkSusanne Thiele, Giovanna Mantovani, Anne Barlier, et al.
European Journal of Endocrinology|August 7, 2017
DIAGNOSIS OF ENDOCRINE DISEASE: Primary empty sella: a comprehensive reviewS Chiloiro, A Giampietro, A Bianchi, et al.
European Journal of Endocrinology|August 7, 2017
Analysis of genetic and clinical characteristics of a Chinese Kallmann syndrome cohort with ANOS1 mutationsMin Nie, Hongli Xu, Rongrong Chen, et al.
European Journal of Endocrinology|August 7, 2017
Bone microarchitecture and estimated bone strength in men with active acromegalyPaula P B Silva, Fatemeh G Amlashi, Elaine W Yu, et al.
European Journal of Endocrinology|June 24, 2016
Impaired growth and intracranial calcifications in autosomal dominant hypocalcemia caused by a GNA11 mutationSirpa Tenhola, Raimo Voutilainen, Monica Reyes, et al.
European Journal of Endocrinology|June 24, 2016
Surgical cure rates of sporadic medullary thyroid cancer in the era of calcitonin screeningAndreas Machens, Henning Dralle
European Journal of Endocrinology|May 12, 2016
Double adrenocortical adenomas harboring independent KCNJ5 and PRKACA somatic mutationsKazutaka Nanba, Kei Omata, Scott A Tomlins, et al.
European Journal of Endocrinology|May 13, 2016
MANAGEMENT OF ENDOCRINE DISEASE: Secondary polycystic ovary syndrome: theoretical and practical aspectsRenato Pasquali, Evanthia Diamanti-Kandarakis, Alessandra Gambineri
European Journal of Endocrinology|May 18, 2016
Molecular CYP21A2 diagnosis in 480 Brazilian patients with congenital adrenal hyperplasia before newborn screening introductionDaniel F de Carvalho, Mirela C Miranda, Larissa G Gomes, et al.
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