These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

106 related items for PubMed ID: 20371198

  • 21. Mitochondrial fatty acid beta-oxidation in the human eye and brain: implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Tyni T, Paetau A, Strauss AW, Middleton B, Kivelä T.
    Pediatr Res; 2004 Nov; 56(5):744-50. PubMed ID: 15347768
    [Abstract] [Full Text] [Related]

  • 22. Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiency.
    van Maldegem BT, Duran M, Wanders RJ, Waterham HR, Wijburg FA.
    Pediatr Res; 2010 Mar; 67(3):304-8. PubMed ID: 19952864
    [Abstract] [Full Text] [Related]

  • 23. Clinical outcomes of infants with short-chain acyl-coenzyme A dehydrogenase deficiency (SCADD) detected by newborn screening.
    Jethva R, Ficicioglu C.
    Mol Genet Metab; 2008 Dec; 95(4):241-2. PubMed ID: 18951053
    [No Abstract] [Full Text] [Related]

  • 24. Vulnerability to oxidative stress in vitro in pathophysiology of mitochondrial short-chain acyl-CoA dehydrogenase deficiency: response to antioxidants.
    Zolkipli Z, Pedersen CB, Lamhonwah AM, Gregersen N, Tein I.
    PLoS One; 2011 Apr 01; 6(4):e17534. PubMed ID: 21483766
    [Abstract] [Full Text] [Related]

  • 25. Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiency.
    Cornelius N, Byron C, Hargreaves I, Guerra PF, Furdek AK, Land J, Radford WW, Frerman F, Corydon TJ, Gregersen N, Olsen RK.
    Hum Mol Genet; 2013 Oct 01; 22(19):3819-27. PubMed ID: 23727839
    [Abstract] [Full Text] [Related]

  • 26. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
    Stanley CA.
    Adv Pediatr; 1987 Oct 01; 34():59-88. PubMed ID: 3318304
    [Abstract] [Full Text] [Related]

  • 27. Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduria.
    Pedersen CB, Zolkipli Z, Vang S, Palmfeldt J, Kjeldsen M, Stenbroen V, Schmidt SP, Wanders RJ, Ruiter JP, Wibrand F, Tein I, Gregersen N.
    J Inherit Metab Dis; 2010 Jun 01; 33(3):211-22. PubMed ID: 20443061
    [Abstract] [Full Text] [Related]

  • 28. A new case of short-chain acyl-CoA dehydrogenase deficiency: clinical, biochemical, genetic and (1)H-NMR spectroscopic studies.
    Battisti C, Forte F, Molinelli M, Funghini S, Pasquini E, Tassini M, Dotti MT, Federico A.
    Neurol Sci; 2007 Dec 01; 28(6):328-30. PubMed ID: 18175080
    [Abstract] [Full Text] [Related]

  • 29. Expression of short-chain acyl-CoA dehydrogenase (SCAD) proteins in the liver of SCAD deficient mice after hydrodynamic gene transfer.
    Holm DA, Dagnaes-Hansen F, Simonsen H, Gregersen N, Bolund L, Jensen TG, Corydon TJ.
    Mol Genet Metab; 2003 Apr 01; 78(4):250-8. PubMed ID: 12706376
    [Abstract] [Full Text] [Related]

  • 30. Clinical relevance of short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Exploring the role of new variants including the first SCAD-disease-causing allele carrying a synonymous mutation.
    Tonin R, Caciotti A, Funghini S, Pasquini E, Mooney SD, Cai B, Proncopio E, Donati MA, Baronio F, Bettocchi I, Cassio A, Biasucci G, Bordugo A, la Marca G, Guerrini R, Morrone A.
    BBA Clin; 2016 Jun 01; 5():114-9. PubMed ID: 27051597
    [Abstract] [Full Text] [Related]

  • 31. Ethylmalonic aciduria is associated with an amino acid variant of short chain acyl-coenzyme A dehydrogenase.
    Corydon MJ, Gregersen N, Lehnert W, Ribes A, Rinaldo P, Kmoch S, Christensen E, Kristensen TJ, Andresen BS, Bross P, Winter V, Martinez G, Neve S, Jensen TG, Bolund L, Kølvraa S.
    Pediatr Res; 1996 Jun 01; 39(6):1059-66. PubMed ID: 8725270
    [Abstract] [Full Text] [Related]

  • 32. Short-chain acyl-CoA dehydrogenase deficiency associated with early onset severe axonal neuropathy.
    Kurian MA, Hartley L, Zolkipli Z, Little MA, Costigan D, Naughten ER, Olpin S, Muntoni F, King MD.
    Neuropediatrics; 2004 Oct 01; 35(5):312-6. PubMed ID: 15534767
    [Abstract] [Full Text] [Related]

  • 33. The 625G>A SCAD gene variant is common but not associated with increased C4-carnitine in newborn blood spots.
    van Maldegem BT, Waterham HR, Duran M, van der Vlies M, van Woerden CS, Bobu LL, Wanders RJ, Wijburg FA.
    J Inherit Metab Dis; 2005 Oct 01; 28(4):557-62. PubMed ID: 15902559
    [Abstract] [Full Text] [Related]

  • 34. Functional analysis of acyl-CoA dehydrogenase catalytic residue mutants using surface plasmon resonance and circular dichroism.
    Goetzman ES, He M, Nguyen TV, Vockley J.
    Mol Genet Metab; 2006 Mar 01; 87(3):233-42. PubMed ID: 16376132
    [Abstract] [Full Text] [Related]

  • 35. Short chain acyl-coenzyme A dehydrogenase (SCAD) deficiency. Immunochemical demonstration of molecular heterogeneity due to variant SCAD with differing stability.
    Naito E, Indo Y, Tanaka K.
    J Clin Invest; 1989 Nov 01; 84(5):1671-4. PubMed ID: 2808706
    [Abstract] [Full Text] [Related]

  • 36. Effect of heat stress and bezafibrate on mitochondrial beta-oxidation: comparison between cultured cells from normal and mitochondrial fatty acid oxidation disorder children using in vitro probe acylcarnitine profiling assay.
    Li H, Fukuda S, Hasegawa Y, Kobayashi H, Purevsuren J, Mushimoto Y, Yamaguchi S.
    Brain Dev; 2010 May 01; 32(5):362-70. PubMed ID: 19589653
    [Abstract] [Full Text] [Related]

  • 37. Detection of allele frequencies of common c. 511C>T and c.625G>A variants in the ACADS gene in the Turkish population.
    Kılıç M, Ergüner B, Koşukçu C, Özgül RK.
    Turk J Pediatr; 2020 May 01; 62(1):19-23. PubMed ID: 32253862
    [Abstract] [Full Text] [Related]

  • 38. Flavine adenine dinucleotide inhibits pathological cardiac hypertrophy and fibrosis through activating short chain acyl-CoA dehydrogenase.
    Ma Z, Qin X, Zhong X, Liao Y, Su Y, Liu X, Liu P, Lu J, Zhou S.
    Biochem Pharmacol; 2020 Aug 01; 178():114100. PubMed ID: 32540485
    [Abstract] [Full Text] [Related]

  • 39. Short- and long-term alterations of mitochondrial morphology, dynamics and mtDNA after transient oxidative stress.
    Jendrach M, Mai S, Pohl S, Vöth M, Bereiter-Hahn J.
    Mitochondrion; 2008 Sep 01; 8(4):293-304. PubMed ID: 18602028
    [Abstract] [Full Text] [Related]

  • 40. [Effects of short-chain acyl-CoA dehydrogenase on human umbilical vein endothelial cell apoptosis].
    Li Z, Shu Z, Liao Y, Liu P, Lu J, Wang P, Wang G, Zang L, Zhou S.
    Zhonghua Wei Zhong Bing Ji Jiu Yi Xue; 2019 Jun 01; 31(6):756-761. PubMed ID: 31315737
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 6.