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European Reference Networks: challenges and opportunities2021 Journal of Community Genetics article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access
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Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients2021 Journal of Endocrinological Investigation article Immunology and Microbiology Immunodeficiency and Autoimmune Disorders Open access
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Diagnosis and management of hypertension in patients with Cushing's syndrome: a position statement and consensus of the Working Group on Endocrine Hypertension of the European Society of Hypertension
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49citations -
Central Adrenal Insufficiency Is Rare in Adults With Prader–Willi Syndrome2020 The Journal of Clinical Endocrinology & Metabolism article Medicine Adrenal Hormones and Disorders Open access
Anna G. W. Rosenberg, Karlijn Pellikaan, Christine Poitou, Anthony Peter Goldstone, Charlotte Höybye, Tania Markovic, +7 more
45citations -
Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development2024 EBioMedicine article Biochemistry, Genetics and Molecular Biology Sexual Differentiation and Disorders Open access
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Hypogonadism in Women with Prader-Willi Syndrome—Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion2021 Journal of Clinical Medicine article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
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29citations -
Hypogonadism in Adult Males with Prader-Willi Syndrome—Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion
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28citations -
Impact of exenatide on weight loss and eating behavior in adults with craniopharyngioma-related obesity: the CRANIOEXE randomized placebo-controlled trial2024 European Journal of Endocrinology article Medicine Pharmacology and Obesity Treatment Open access
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ESE audit on management of adult growth hormone deficiency in clinical practice2020 European Journal of Endocrinology article Medicine Growth Hormone and Insulin-like Growth Factors Open access
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Health Problems in Adults with Prader–Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the Literature2022 Journal of Clinical Medicine article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
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22citations -
An overview of clinical activities in Endo-ERN: the need for alignment of future network criteria2020 European Journal of Endocrinology article Business, Management and Accounting Healthcare Systems and Technology Open access
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Bone Health in Adults With Prader–Willi Syndrome: Clinical Recommendations Based on a Multicenter Cohort Study2022 The Journal of Clinical Endocrinology & Metabolism article Medicine Bone health and osteoporosis research Open access
Denise H. van Abswoude, Karlijn Pellikaan, Anna G. W. Rosenberg, Kirsten Davidse, Muriel Coupaye, Charlotte Höybye, +13 more
20citations -
Improved Oral Health in Adults With X-Linked Hypophosphatemia Treated With Burosumab2024 The Journal of Clinical Endocrinology & Metabolism article Medicine Parathyroid Disorders and Treatments
Agathe Hervé, Margaux Gadion, Julia Herrou, Mathieu Izart, Agnès Linglart, Martine Esther Cohen-Solal, +5 more
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Starting point for benchmarking outcomes and reporting of pituitary adenoma surgery within the European Reference Network on Rare Endocrine Conditions (Endo-ERN): results from a meta-analysis and survey study
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An update on the long-term outcomes of prenatal dexamethasone treatment in congenital adrenal hyperplasia2023 Endocrine Connections article Biochemistry, Genetics and Molecular Biology Sexual Differentiation and Disorders Open access
Annelies van’t Westeinde, Leif Karlsson, Valeria Messina, Lena Wallensteen, Manuela Brösamle, Giorgio Dal Maso, +9 more
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Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review2023 The Journal of Clinical Endocrinology & Metabolism article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Karlijn Pellikaan, Naomi Nguyen, Anna G. W. Rosenberg, Muriel Coupaye, Anthony Peter Goldstone, Charlotte Höybye, +9 more
13citations