Laura C. G. de Graaff

Missed Diagnoses and Health Problems in Adults With Prader-Willi Syndrome: Recommendations for Screening and Treatment

Karlijn Pellikaan, Anna G. W. Rosenberg, Anja A. Kattentidt‐Mouravieva et al. · The Journal of Clinical Endocrinology & Metabolism · 2020 · 53 citations · Full text

Medicine, Endocrinology, Internal Medicine +17

A novel OTX2 mutation in a patient with combined pituitary hormone deficiency, pituitary malformation, and an underdeveloped left optic nerve

Darya Gorbenko del Blanco, Christopher Romero, Daniel Diaczok et al. · European Journal of Endocrinology · 2012 · 44 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Central Adrenal Insufficiency Is Rare in Adults With Prader–Willi Syndrome

Anna G. W. Rosenberg, Karlijn Pellikaan, Christine Poitou et al. · The Journal of Clinical Endocrinology & Metabolism · 2020 · 44 citations · Full text

Medicine, Endocrinology, Internal Medicine +14

A value‐based healthcare approach: Health‐related quality of life and psychosocial functioning in women with Turner syndrome

Allard T. van den Hoven, Lidia R. Bons, Ramon Dykgraaf et al. · Clinical Endocrinology · 2020 · 35 citations · Full text

Pharmacy, Health Sciences, Health Assessment +16

Growth Hormone Treatment for Adults With Prader-Willi Syndrome: A Meta-Analysis

Anna G. W. Rosenberg, Karlijn Pellikaan, Durval Damiani et al. · The Journal of Clinical Endocrinology & Metabolism · 2021 · 34 citations · Full text

Medicine, Endocrinology, Pediatrics +15