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Page 1
Leukocyte Telomere Length in Children With Congenital Adrenal Hyperplasia.
Raftopoulou C, Abawi O, Sommer G, Binou M, Paltoglou G, Flück CE, van den Akker ELT, Charmandari E. Raftopoulou C, et al. Among authors: van den akker elt. J Clin Endocrinol Metab. 2023 Jan 17;108(2):443-452. doi: 10.1210/clinem/dgac560. J Clin Endocrinol Metab. 2023. PMID: 36181470 Free article.
Blood pressure and its associations in 554 children and young people with congenital adrenal hyperplasia.
Lawrence NR, Bacila I, Tonge J, Dawson J, Collins GS, Lang ZQ, Bryce J, Alimussina M, Chen M, Ali SR, Adam S, van den Akker ELT, Bachega TASS, Baronio F, Birkebæk NH, Bonfig W, Claahsen-van der Grinten H, Cools M, Costa EC, Debono M, de Vries L, Flück CE, Gazdagh G, Güven A, Hannema SE, Iotova V, van der Kamp HJ, Krone R, Leka-Emiri S, Clemente-León M, Lichiardopol CR, Markosyan RL, Milenkovic T, de Miranda MC, Neumann U, Newell-Price J, Poyrazoğlu Ş, Probst-Scheidegger U, Russo G, De Sanctis L, Seneviratne SN, Stancampiano MR, Tadokoro-Cuccaro R, Thankamony A, Vieites A, Wasniewska M, Yeste D, Tomlinson J, Ahmed SF, Krone N. Lawrence NR, et al. Among authors: van den akker elt. Eur J Endocrinol. 2025 Apr 30;192(5):529-539. doi: 10.1093/ejendo/lvaf060. Eur J Endocrinol. 2025. PMID: 40184493 Free article.
Evaluation of the Dutch neonatal screening for congenital adrenal hyperplasia.
van der Linde AAA, Schönbeck Y, van der Kamp HJ, van den Akker ELT, van Albada ME, Boelen A, Finken MJJ, Hannema SE, Hoorweg-Nijman G, Odink RJ, Schielen PCJI, Straetemans S, van Trotsenburg PS, Claahsen-van der Grinten HL, Verkerk PH. van der Linde AAA, et al. Among authors: van den akker elt, van trotsenburg ps, van der kamp hj, van albada me. Arch Dis Child. 2019 Jul;104(7):653-657. doi: 10.1136/archdischild-2018-315972. Epub 2019 Feb 2. Arch Dis Child. 2019. PMID: 30712004
Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry.
Lawrence N, Bacila I, Dawson J, Bryce J, Ali SR, van den Akker ELT, Bachega TASS, Baronio F, Birkebaek NH, Bonfig W, van der Grinten HC, Costa EC, de Vries L, Elsedfy H, Güven A, Hannema S, Iotova V, van der Kamp HJ, Clemente M, Lichiardopol CR, Milenkovic T, Neumann U, Nordenström A, Poyrazoğlu Ş, Probst-Scheidegger U, De Sanctis L, Tadokoro-Cuccaro R, Thankamony A, Vieites A, Yavaş Z, Faisal Ahmed S, Krone N. Lawrence N, et al. Among authors: van der grinten hc, van den akker elt, van der kamp hj. Clin Endocrinol (Oxf). 2022 Nov;97(5):551-561. doi: 10.1111/cen.14796. Epub 2022 Jul 11. Clin Endocrinol (Oxf). 2022. PMID: 35781728 Free PMC article.
Resting Energy Expenditure and Body Composition in Children and Adolescents With Genetic, Hypothalamic, Medication-Induced or Multifactorial Severe Obesity.
Abawi O, Koster EC, Welling MS, Boeters SCM, van Rossum EFC, van Haelst MM, van der Voorn B, de Groot CJ, van den Akker ELT. Abawi O, et al. Among authors: van rossum efc, van haelst mm, van den akker elt, van der voorn b. Front Endocrinol (Lausanne). 2022 Jul 11;13:862817. doi: 10.3389/fendo.2022.862817. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35898454 Free PMC article.
Loss-of-Function GHSR Variants Are Associated With Short Stature and Low IGF-I.
Punt LD, Kooijman S, Mutsters NJM, Yue K, van der Kaay DCM, van Tellingen V, Bakker-van Waarde WM, Boot AM, van den Akker ELT, van Boekholt AA, de Groote K, Kruijsen AR, van Nieuwaal-van Maren NHG, Woltering MC, Heijligers M, van der Heyden JC, Bannink EMN, Rinne T, Hannema SE, de Waal WJ, Delemarre LC, Rensen PCN, de Bruin C, van Duyvenvoorde HA, Visser JA, Delhanty PJD, Losekoot M, Wit JM, Joustra SD. Punt LD, et al. Among authors: van den akker elt. J Clin Endocrinol Metab. 2025 Apr 22;110(5):e1303-e1314. doi: 10.1210/clinem/dgaf010. J Clin Endocrinol Metab. 2025. PMID: 39785833 Free PMC article.
Second case of Bardet-Biedl syndrome caused by biallelic variants in IFT74.
Kleinendorst L, Alsters SIM, Abawi O, Waisfisz Q, Boon EMJ, van den Akker ELT, van Haelst MM. Kleinendorst L, et al. Among authors: van haelst mm, van den akker elt. Eur J Hum Genet. 2020 Jul;28(7):943-946. doi: 10.1038/s41431-020-0594-z. Epub 2020 Mar 6. Eur J Hum Genet. 2020. PMID: 32144365 Free PMC article.
Second-tier Testing for 21-Hydroxylase Deficiency in the Netherlands: A Newborn Screening Pilot Study.
Stroek K, Ruiter A, van der Linde A, Ackermans M, Bouva MJ, Engel H, Jakobs B, Kemper EA, van den Akker ELT, van Albada ME, Bocca G, Finken MJJ, Hannema SE, Mieke Houdijk ECA, van der Kamp HJ, van Tellingen V, Paul van Trotsenburg AS, Zwaveling-Soonawala N, Bosch AM, de Jonge R, Heijboer AC, Claahsen-van der Grinten HL, Boelen A. Stroek K, et al. Among authors: van der linde a, van tellingen v, van den akker elt, van der kamp hj, van albada me. J Clin Endocrinol Metab. 2021 Oct 21;106(11):e4487-e4496. doi: 10.1210/clinem/dgab464. J Clin Endocrinol Metab. 2021. PMID: 34171085
170 results