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Hormones (Athens, Greece)|June 3, 2018
Two rare forms of congenital adrenal hyperplasia, 11β hydroxylase deficiency and 17-hydroxylase/17,20-lyase deficiency, presenting with novel mutationsKrupali Bulsari, Louise Maple-Brown, Henrik FalhammarFrontiers in Endocrinology|February 7, 2025
Sex differences in presentation of pheochromocytoma and paragangliomaNora Azin Ali, Jan Calissendorff, Henrik FalhammarClinical Endocrinology|July 11, 2025
Differences in Clinical Presentation Between Pheochromocytomas and ParagangliomasVincent E D Pihlblad, Jan Calissendorff, Henrik FalhammarEndocrine|November 14, 2022
Hypoglycemia after exposure of diclofenac medicationHenrik Falhammar, Ove Törring, Martin Larsson, et al.Endocrine|February 2, 2024
Surgical outcome after thyroidectomy due to Graves' disease and Lugol iodine treatment: a retrospective register-based cohort studyFredric Hedberg, Henrik Falhammar, Jan Calissendorff, et al.Endocrine|October 17, 2014
Ileal neuroendocrine tumors and heart: not only valvular consequencesJan Calissendorff, Eva Maret, Anders Sundin, et al.Frontiers in Endocrinology|September 9, 2020
Bone Mineral Density in Adults With Congenital Adrenal Hyperplasia: A Systematic Review and Meta-AnalysisSwetha Rangaswamaiah, Vinay Gangathimmaiah, Anna Nordenstrom, et al.Clinical Endocrinology|February 19, 2021
First insights into the genetics of 21-hydroxylase deficiency in the Roma populationMirjana Kocova, Violeta Anastasovska, Aleksandar Petlichkovski, et al.Endocrine|September 10, 2017
Increased mortality in patients with adrenal incidentalomas and autonomous cortisol secretion: a 13-year retrospective study from one centerJekaterina Patrova, Magnus Kjellman, Hans Wahrenberg, et al.Endocrine|December 21, 2016
Adrenal crises: perspectives and research directionsR Louise Rushworth, David J Torpy, Henrik FalhammarPageof 27