Aart J van der Lely
Overview
Explore the profile of Aart J van der Lely including associated specialties, affiliations and a list of published articles.
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61
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1258
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Recent Articles
1.
Rosenberg A, Mochel K, Hahner L, Ruules L, Davidse K, Bos-Roubos A, et al.
Front Endocrinol (Lausanne)
. 2024 Apr;
14:1119159.
PMID: 38560379
Context: Neurofibromatosis type 1 (NF1) is a complex system disorder, caused by alterations in RAS pathways. NF1 adults often suffer from chronic and severe fatigue, for which they are frequently...
2.
van Abswoude D, Pellikaan K, Nguyen N, Rosenberg A, Davidse K, Hoekstra F, et al.
Front Endocrinol (Lausanne)
. 2024 Feb;
15:1357219.
PMID: 38318297
[This corrects the article DOI: 10.3389/fendo.2023.1168648.].
3.
Nijenhuis-Noort E, Berk K, Neggers S, van der Lely A
Endocrinol Metab (Seoul)
. 2024 Jan;
39(1):83-89.
PMID: 38192102
This review intends to provide the reader with a practical overview of several (patho)physiological conditions in which knowledge of the interplay between growth hormone (GH), insulin-like growth factor-1 (IGF-1), and...
4.
van Abswoude D, Pellikaan K, Nguyen N, Rosenberg A, Davidse K, Hoekstra F, et al.
Front Endocrinol (Lausanne)
. 2023 Aug;
14:1168648.
PMID: 37547314
Background: Prader-Willi syndrome (PWS) is a rare, complex, genetic disorder characterized by hyperphagia, hypotonia, delayed psychomotor development, low muscle mass and hypothalamic dysfunction. Adults with PWS often have obesity, hypertension...
5.
Rosenberg A, Dingemans V, Bos-Roubos A, Luijks S, Dessens A, Dykgraaf R, et al.
J Clin Endocrinol Metab
. 2023 Jun;
108(12):e1649-e1659.
PMID: 37296515
Context: Turner syndrome (TS) is a rare chromosomal disorder characterized by gonadal dysfunction, short stature, and heart defects, among other features. Women with TS often suffer from severe fatigue, for...
6.
Pellikaan K, Nguyen N, Rosenberg A, Coupaye M, Goldstone A, Hoybye C, et al.
J Clin Endocrinol Metab
. 2023 Jun;
108(12):e1720-e1730.
PMID: 37267430
Context: Prader-Willi syndrome (PWS) is a complex disorder combining hypothalamic dysfunction, neurodevelopmental delay, hypotonia, and hyperphagia with risk of obesity and its complications. PWS is caused by the loss of...
7.
Pellikaan K, van Weijen P, Rosenberg A, Hoekstra F, Vermaak M, Oomen P, et al.
Front Endocrinol (Lausanne)
. 2023 Apr;
14:1145066.
PMID: 37033248
Context: Prader-Willi syndrome (PWS) is a complex rare genetic syndrome. Mortality in patients with PWS is 3% per year. In nearly half of the patients, the cause of death is...
8.
van Abswoude D, Pellikaan K, Rosenberg A, Davidse K, Coupaye M, Hoybye C, et al.
J Clin Endocrinol Metab
. 2022 Sep;
108(1):59-84.
PMID: 36149817
Context: Prader-Willi syndrome (PWS) is a rare complex genetic syndrome, characterized by delayed psychomotor development, hypotonia, and hyperphagia. Hormone deficiencies such as hypogonadism, hypothyroidism, and growth hormone deficiency are common....
9.
Rosenberg A, Langendoen W, van der Lely A, Veenland J, de Graaff L
Eur J Intern Med
. 2022 Sep;
106:154-157.
PMID: 36064637
No abstract available.
10.
Rosenberg A, Wellink C, Tellez Garcia J, Pellikaan K, van Abswoude D, Davidse K, et al.
J Clin Med
. 2022 Jul;
11(14).
PMID: 35887798
Prader−Willi syndrome (PWS) is a complex, rare genetic disorder caused by a loss of expression of paternally expressed genes on chromosome 15q11.2-q13. The most common underlying genotypes are paternal deletion...