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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2003 | 1 |
2009 | 1 |
2011 | 1 |
2013 | 1 |
2018 | 1 |
2024 | 0 |
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MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency.
J Pediatr. 2003 Sep;143(3):335-42. doi: 10.1067/S0022-3476(03)00292-0.
J Pediatr. 2003.
PMID: 14517516
Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiency.
Laforêt P, Acquaviva-Bourdain C, Rigal O, Brivet M, Penisson-Besnier I, Chabrol B, Chaigne D, Boespflug-Tanguy O, Laroche C, Bedat-Millet AL, Behin A, Delevaux I, Lombès A, Andresen BS, Eymard B, Vianey-Saban C.
Laforêt P, et al.
Neuromuscul Disord. 2009 May;19(5):324-9. doi: 10.1016/j.nmd.2009.02.007. Epub 2009 Mar 26.
Neuromuscul Disord. 2009.
PMID: 19327992
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Positive newborn screen in a normal infant of a mother with asymptomatic very long-chain Acyl-CoA dehydrogenase deficiency.
McGoey RR, Marble M.
McGoey RR, et al.
J Pediatr. 2011 Jun;158(6):1031-2. doi: 10.1016/j.jpeds.2011.01.063. Epub 2011 Mar 22.
J Pediatr. 2011.
PMID: 21429517
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Neuropsychological outcomes in fatty acid oxidation disorders: 85 cases detected by newborn screening.
Waisbren SE, Landau Y, Wilson J, Vockley J.
Waisbren SE, et al.
Dev Disabil Res Rev. 2013;17(3):260-8. doi: 10.1002/ddrr.1119.
Dev Disabil Res Rev. 2013.
PMID: 23798014
Free PMC article.
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The diagnostic challenge in very-long chain acyl-CoA dehydrogenase deficiency (VLCADD).
Hesse J, Braun C, Behringer S, Matysiak U, Spiekerkoetter U, Tucci S.
Hesse J, et al.
J Inherit Metab Dis. 2018 Nov;41(6):1169-1178. doi: 10.1007/s10545-018-0245-5. Epub 2018 Sep 7.
J Inherit Metab Dis. 2018.
PMID: 30194637
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