F. Boer

Clinical and biochemical heterogeneity between patients with glycogen storage disease type

T. Derks, M. Oosterveer, D. A. Weinstein, 2017 .

A retrospective study of eating and psychosocial problems in patients with hepatic glycogen storage diseases and idiopathic ketotic hypoglycemia: Towards a standard set of patient‐reported outcome measures

F. de Boer, T. Derks, B. Huskens, 2021, JIMD reports.

Dietary practices in methylmalonic acidaemia: a European survey

F. Eyskens, D. Cassiman, A. Schlune, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

A retrospective in‐depth analysis of continuous glucose monitoring datasets for patients with hepatic glycogen storage disease: Recommended outcome parameters for glucose management

M. M. van der Klauw, Irene J. Hoogeveen, F. de Boer, 2021, Journal of inherited metabolic disease.

Dietary practices in propionic acidemia: A European survey

F. Eyskens, D. Cassiman, A. Schlune, 2017, Molecular genetics and metabolism reports.

Clinical and biochemical heterogeneity between patients with glycogen storage disease type IA: the added value of CUSUM for metabolic control

F. de Boer, T. Derks, M. Oosterveer, 2017, Journal of Inherited Metabolic Disease.

International practices in the dietary management of fructose 1-6 biphosphatase deficiency

F. de Boer, M. Dixon, A. Macdonald, 2018, Orphanet Journal of Rare Diseases.