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2018 3
2019 3
2020 3
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Page 1
Biomarkers of Micronutrients in Regular Follow-Up for Tyrosinemia Type 1 and Phenylketonuria Patients.
van Vliet K, Rodenburg IL, van Ginkel WG, Lubout CMA, Wolffenbuttel BHR, van der Klauw MM, Heiner-Fokkema MR, van Spronsen FJ. van Vliet K, et al. Among authors: lubout cma. Nutrients. 2019 Aug 27;11(9):2011. doi: 10.3390/nu11092011. Nutrients. 2019. PMID: 31461828 Free PMC article.
Safety issues associated with dietary management in patients with hepatic glycogen storage disease.
Steunenberg TAH, Peeks F, Hoogeveen IJ, Mitchell JJ, Mundy H, de Boer F, Lubout CMA, de Souza CF, Weinstein DA, Derks TGJ. Steunenberg TAH, et al. Among authors: lubout cma. Mol Genet Metab. 2018 Sep;125(1-2):79-85. doi: 10.1016/j.ymgme.2018.07.004. Epub 2018 Jul 18. Mol Genet Metab. 2018. PMID: 30037503 Free article.
Molybdenum cofactor deficiency type A: Prenatal monitoring using MRI.
Lubout CMA, Derks TGJ, Meiners L, Erwich JJ, Bergman KA, Lunsing RJ, Schwarz G, Veldman A, van Spronsen FJ. Lubout CMA, et al. Eur J Paediatr Neurol. 2018 May;22(3):536-540. doi: 10.1016/j.ejpn.2017.11.006. Epub 2017 Nov 28. Eur J Paediatr Neurol. 2018. PMID: 29274890
Bone mineral density is within normal range in most adult phenylketonuria patients.
Lubout CMA, Arrieta Blanco F, Bartosiewicz K, Feillet F, Gizewska M, Hollak C, van der Lee JH, Maillot F, Stepien KM, Wagenmakers MAEM, Welsink-Karssies MM, van Spronsen FJ, Bosch AM. Lubout CMA, et al. J Inherit Metab Dis. 2020 Mar;43(2):251-258. doi: 10.1002/jimd.12177. Epub 2020 Feb 6. J Inherit Metab Dis. 2020. PMID: 31587319 Free PMC article.
A preliminary study of telemedicine for patients with hepatic glycogen storage disease and their healthcare providers: from bedside to home site monitoring.
Hoogeveen IJ, Peeks F, de Boer F, Lubout CMA, de Koning TJ, Te Boekhorst S, Zandvoort RJ, Burghard R, van Spronsen FJ, Derks TGJ. Hoogeveen IJ, et al. Among authors: lubout cma. J Inherit Metab Dis. 2018 Nov;41(6):929-936. doi: 10.1007/s10545-018-0167-2. Epub 2018 Mar 29. J Inherit Metab Dis. 2018. PMID: 29600495 Free PMC article.
The first European guidelines on phenylketonuria: Usefulness and implications for BH4 responsiveness testing.
Evers RAF, van Wegberg AMJ, Anjema K, Lubout CMA, van Dam E, van Vliet D, Blau N, van Spronsen FJ. Evers RAF, et al. Among authors: lubout cma. J Inherit Metab Dis. 2020 Mar;43(2):244-250. doi: 10.1002/jimd.12173. Epub 2019 Nov 20. J Inherit Metab Dis. 2020. PMID: 31503351
Successful Treatment of Hereditary Folate Malabsorption With Intramuscular Folinic Acid.
Lubout CMA, Goorden SMI, van den Hurk K, Jaeger B, Jager NGL, van Koningsbruggen S, Chegary M, van Karnebeek CDM. Lubout CMA, et al. Pediatr Neurol. 2020 Jan;102:62-66. doi: 10.1016/j.pediatrneurol.2019.06.009. Epub 2019 Jun 22. Pediatr Neurol. 2020. PMID: 31371121
Cervical high-intensity intramedullary lesions in achondroplasia: aetiology, prevalence and clinical relevance.
Brouwer PA, Lubout CM, van Dijk JM, Vleggeert-Lankamp CL. Brouwer PA, et al. Among authors: lubout cm. Eur Radiol. 2012 Oct;22(10):2264-72. doi: 10.1007/s00330-012-2488-0. Epub 2012 May 26. Eur Radiol. 2012. PMID: 22638916 Free PMC article.