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BMC Endocrine Disorders|March 18, 2016
Adrenocortical cancer: mortality, hormone secretion, proliferation and urine steroids - experience from a single centre spanning three decadesJan Calissendorff, Freja Calissendorff, Henrik FalhammarEndocrine|September 17, 2018
Treatment and outcomes in pheochromocytomas and paragangliomas: a study of 110 cases from a single centerHenrik Falhammar, Magnus Kjellman, Jan CalissendorffEndocrine|August 25, 2012
Thyrotoxic periodic paralysis: clinical and molecular aspectsHenrik Falhammar, Marja Thorén, Jan CalissendorffExpert Review of Endocrinology & Metabolism|November 21, 2024
Adrenocortical tumors and hereditary syndromesKanakamani Jeyaraman, Paola Concolino, Henrik FalhammarEndocrine|September 5, 2015
Biochemical and genetic diagnosis of 21-hydroxylase deficiencyHenrik Falhammar, Anna Wedell, Anna NordenströmFrontiers in Endocrinology|December 22, 2022
Congenital adrenal hyperplasia is a very rare cause of adrenal incidentalomas in SwedenFredrik Sahlander, Sophie Bensing, Henrik FalhammarHormone Research in Paediatrics|January 27, 2022
Current and Novel Treatment Strategies in Children with Congenital Adrenal HyperplasiaAnna Nordenström, Henrik Falhammar, Svetlana LajicBMC Endocrine Disorders|December 4, 2019
Acute suppurative thyroiditis with thyroid abscess in adults: clinical presentation, treatment and outcomesHenrik Falhammar, Göran Wallin, Jan CalissendorffCurrent Opinion in Endocrinology, Diabetes, and Obesity|March 20, 2021
Clinical outcomes in 21-hydroxylase deficiencyAnna Nordenström, Svetlana Lajic, Henrik FalhammarThe Journal of Clinical Endocrinology and Metabolism|March 20, 2018
Bilateral Adrenalectomy in Congenital Adrenal Hyperplasia: A Systematic Review and Meta-AnalysisDiana MacKay, Anna Nordenström, Henrik FalhammarPageof 27