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1. A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome. (1st October 2018)

2. Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study. Issue 7 (July 2020)

3. Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study. Issue 7 (July 2020)

4. Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial. Issue 9 (September 2019)

5. Familial dysalbuminaemic hyperthyroxinaemia interferes with current free thyroid hormone immunoassay methods. Issue 6 (June 2020)

6. Familial dysalbuminaemic hyperthyroxinaemia interferes with current free thyroid hormone immunoassay methods. Issue 6 (June 2020)