105 related articles for article (PubMed ID: 15249642)
1. Tremor and deep white matter changes in alpha-methylacyl-CoA racemase deficiency.
Clarke CE; Alger S; Preece MA; Burdon MA; Chavda S; Denis S; Ferdinandusse S; Wanders RJ
Neurology; 2004 Jul; 63(1):188-9. PubMed ID: 15249642
[No Abstract] [Full Text] [Related]
2. A new defect of peroxisomal function involving pristanic acid: a case report.
McLean BN; Allen J; Ferdinandusse S; Wanders RJ
J Neurol Neurosurg Psychiatry; 2002 Mar; 72(3):396-9. PubMed ID: 11861706
[TBL] [Abstract][Full Text] [Related]
3. Stereochemistry of the peroxisomal branched-chain fatty acid alpha- and beta-oxidation systems in patients suffering from different peroxisomal disorders.
Ferdinandusse S; Rusch H; van Lint AE; Dacremont G; Wanders RJ; Vreken P
J Lipid Res; 2002 Mar; 43(3):438-44. PubMed ID: 11893780
[TBL] [Abstract][Full Text] [Related]
4. Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency.
Ferdinandusse S; Overmars H; Denis S; Waterham HR; Wanders RJ; Vreken P
J Lipid Res; 2001 Jan; 42(1):137-41. PubMed ID: 11160375
[TBL] [Abstract][Full Text] [Related]
5. Relapsing rhabdomyolysis due to peroxisomal alpha-methylacyl-coa racemase deficiency.
Kapina V; Sedel F; Truffert A; Horvath J; Wanders RJ; Waterham HR; Picard F
Neurology; 2010 Oct; 75(14):1300-2. PubMed ID: 20921516
[No Abstract] [Full Text] [Related]
6. Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency.
Van Veldhoven PP; Meyhi E; Squires RH; Fransen M; Fournier B; Brys V; Bennett MJ; Mannaerts GP
Eur J Clin Invest; 2001 Aug; 31(8):714-22. PubMed ID: 11473573
[TBL] [Abstract][Full Text] [Related]
7. Relapsing encephalopathy in a patient with alpha-methylacyl-CoA racemase deficiency.
Thompson SA; Calvin J; Hogg S; Ferdinandusse S; Wanders RJ; Barker RA
J Neurol Neurosurg Psychiatry; 2008 Apr; 79(4):448-50. PubMed ID: 18032455
[TBL] [Abstract][Full Text] [Related]
8. An adult onset case of alpha-methyl-acyl-CoA racemase deficiency.
Smith EH; Gavrilov DK; Oglesbee D; Freeman WD; Vavra MW; Matern D; Tortorelli S
J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S349-53. PubMed ID: 20821052
[TBL] [Abstract][Full Text] [Related]
9. MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencing.
Haugarvoll K; Johansson S; Tzoulis C; Haukanes BI; Bredrup C; Neckelmann G; Boman H; Knappskog PM; Bindoff LA
Orphanet J Rare Dis; 2013 Jan; 8():1. PubMed ID: 23286897
[TBL] [Abstract][Full Text] [Related]
10. Identification and diagnostic value of phytanoyl- and pristanoyl-carnitine in plasma from patients with peroxisomal disorders.
Herzog K; van Lenthe H; Wanders RJA; Vaz FM; Waterham HR; Ferdinandusse S
Mol Genet Metab; 2017 Jul; 121(3):279-282. PubMed ID: 28566232
[TBL] [Abstract][Full Text] [Related]
11. A mouse model for alpha-methylacyl-CoA racemase deficiency: adjustment of bile acid synthesis and intolerance to dietary methyl-branched lipids.
Savolainen K; Kotti TJ; Schmitz W; Savolainen TI; Sormunen RT; Ilves M; Vainio SJ; Conzelmann E; Hiltunen JK
Hum Mol Genet; 2004 May; 13(9):955-65. PubMed ID: 15016763
[TBL] [Abstract][Full Text] [Related]
12. Peroxisomes, lipid metabolism, and peroxisomal disorders.
Wanders RJ
Mol Genet Metab; 2004; 83(1-2):16-27. PubMed ID: 15464416
[TBL] [Abstract][Full Text] [Related]
13. Alpha-methylacyl-CoA racemase deletion has mutually counteracting effects on T-cell responses, associated with unchanged course of EAE.
Tafferner N; Barthelmes J; Eberle M; Ulshöfer T; Henke M; deBruin N; Mayer CA; Foerch C; Geisslinger G; Parnham MJ; Schiffmann S
Eur J Immunol; 2016 Mar; 46(3):570-81. PubMed ID: 26648339
[TBL] [Abstract][Full Text] [Related]
14. Incidental finding of alpha-methylacyl-CoA racemase deficiency in a patient with oculocutaneous albinism type 4.
Verhagen JM; Huijmans JG; Williams M; van Ruyven RL; Bergen AA; Wouters CH; Brooks AS
Am J Med Genet A; 2012 Nov; 158A(11):2931-4. PubMed ID: 22987308
[TBL] [Abstract][Full Text] [Related]
15. Alpha-methyl acetyl-coA racemase deficiency. Magnetic resonance imaging findings of three patients with encephalopathy, epilepsy, and stroke-like episodes.
Palacio-Montoya MI; Herrera DA; Vargas SA; Castillo M
Neuroradiol J; 2024 Jun; 37(3):351-356. PubMed ID: 37452652
[TBL] [Abstract][Full Text] [Related]
16. Phytanic acid, AMACR and prostate cancer risk.
Thornburg T; Turner AR; Chen YQ; Vitolins M; Chang B; Xu J
Future Oncol; 2006 Apr; 2(2):213-23. PubMed ID: 16563090
[TBL] [Abstract][Full Text] [Related]
17. Mouse models for peroxisome biogenesis defects and β-oxidation enzyme deficiencies.
Baes M; Van Veldhoven PP
Biochim Biophys Acta; 2012 Sep; 1822(9):1489-500. PubMed ID: 22446031
[TBL] [Abstract][Full Text] [Related]
18. Late onset AMACR deficiency with metabolic stroke-like episodes and seizures.
Tanti MJ; Maguire MJ; Warren DJ; Bamford J
BMJ Case Rep; 2022 Apr; 15(4):. PubMed ID: 35428665
[TBL] [Abstract][Full Text] [Related]
19. Branched fatty acids in dairy and beef products markedly enhance alpha-methylacyl-CoA racemase expression in prostate cancer cells in vitro.
Mobley JA; Leav I; Zielie P; Wotkowitz C; Evans J; Lam YW; L'Esperance BS; Jiang Z; Ho SM
Cancer Epidemiol Biomarkers Prev; 2003 Aug; 12(8):775-83. PubMed ID: 12917210
[TBL] [Abstract][Full Text] [Related]
20. Phytanic acid--an overlooked bioactive fatty acid in dairy fat?
Hellgren LI
Ann N Y Acad Sci; 2010 Mar; 1190():42-9. PubMed ID: 20388135
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
