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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 6
2003 1
2004 1
2005 1
2007 1
2008 1
2009 1
2010 4
2011 3
2012 6
2013 8
2014 12
2015 9
2016 9
2017 6
2018 3
2019 8
2020 12
2021 4
2022 4
2023 4
2024 0

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88 results

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Page 1
Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle.
Knottnerus SJG, Bleeker JC, Wüst RCI, Ferdinandusse S, IJlst L, Wijburg FA, Wanders RJA, Visser G, Houtkooper RH. Knottnerus SJG, et al. Among authors: visser g. Rev Endocr Metab Disord. 2018 Mar;19(1):93-106. doi: 10.1007/s11154-018-9448-1. Rev Endocr Metab Disord. 2018. PMID: 29926323 Free PMC article. Review.
PIGO deficiency: palmoplantar keratoderma and novel mutations.
Morren MA, Jaeken J, Visser G, Salles I, Van Geet C; NIHR BioResource; Simeoni I, Turro E, Freson K. Morren MA, et al. Among authors: visser g. Orphanet J Rare Dis. 2017 May 25;12(1):101. doi: 10.1186/s13023-017-0654-9. Orphanet J Rare Dis. 2017. PMID: 28545593 Free PMC article. Review.
Ketones and inborn errors of metabolism: old friends revisited.
Wüst RC, Visser G, Wanders RJ, Houtkooper RH. Wüst RC, et al. Among authors: visser g. J Inherit Metab Dis. 2017 Jan;40(1):3-4. doi: 10.1007/s10545-016-9997-y. J Inherit Metab Dis. 2017. PMID: 27830424 No abstract available.
[Hereditary fructose intolerance].
Rumping L, Waterham HR, Kok I, van Hasselt PM, Visser G. Rumping L, et al. Among authors: visser g. Ned Tijdschr Geneeskd. 2014;158:A6889. Ned Tijdschr Geneeskd. 2014. PMID: 24594126 Dutch.
Liver transplantation in glycogen storage disease type I.
Boers SJ, Visser G, Smit PG, Fuchs SA. Boers SJ, et al. Among authors: visser g. Orphanet J Rare Dis. 2014 Apr 9;9:47. doi: 10.1186/1750-1172-9-47. Orphanet J Rare Dis. 2014. PMID: 24716823 Free PMC article. Review.
Thermo-sensitive mitochondrial trifunctional protein deficiency presenting with episodic myopathy.
Schwantje M, Ebberink MS, Doolaard M, Ruiter JPN, Fuchs SA, Darin N, Hedberg-Oldfors C, Régal L, Donker Kaat L, Huidekoper HH, Olpin S, Cole D, Moat SJ, Visser G, Ferdinandusse S. Schwantje M, et al. Among authors: visser g. J Inherit Metab Dis. 2022 Jul;45(4):819-831. doi: 10.1002/jimd.12503. Epub 2022 May 5. J Inherit Metab Dis. 2022. PMID: 35403730 Free PMC article.
Identification of human D lactate dehydrogenase deficiency.
Monroe GR, van Eerde AM, Tessadori F, Duran KJ, Savelberg SMC, van Alfen JC, Terhal PA, van der Crabben SN, Lichtenbelt KD, Fuchs SA, Gerrits J, van Roosmalen MJ, van Gassen KL, van Aalderen M, Koot BG, Oostendorp M, Duran M, Visser G, de Koning TJ, Calì F, Bosco P, Geleijns K, de Sain-van der Velden MGM, Knoers NV, Bakkers J, Verhoeven-Duif NM, van Haaften G, Jans JJ. Monroe GR, et al. Among authors: visser g. Nat Commun. 2019 Apr 1;10(1):1477. doi: 10.1038/s41467-019-09458-6. Nat Commun. 2019. PMID: 30931947 Free PMC article.
88 results