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You searched for: Author/Creator Polak, Michel

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11. Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort. (21st December 2020)

12. Clinical, laboratory and molecular findings and long-term follow-up data in 96 French patients with PMM2-CDG (phosphomannomutase 2-congenital disorder of glycosylation) and review of the literature. Issue 12 (27th September 2017)

13. Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations. Issue 11 (6th August 2019)

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

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

17. Early treatment of neonatal diabetes with oral glibenclamide in an extremely preterm infant. Issue 2 (29th January 2023)

18. Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study. Issue 8 (August 2018)

20. 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)