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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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2002 | 1 |
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PubMed (cited) for id: 614307
6 results
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Page 1
AMACR mutations cause late-onset autosomal recessive cerebellar ataxia.
Neurology. 2011 May 17;76(20):1768-70. doi: 10.1212/WNL.0b013e31821a4484.
Neurology. 2011.
PMID: 21576695
Free PMC article.
No abstract available.
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.
Smith EH, et al.
J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S349-53. doi: 10.1007/s10545-010-9183-6. Epub 2010 Sep 4.
J Inherit Metab Dis. 2010.
PMID: 20821052
Item in Clipboard
Relapsing encephalopathy in a patient with alpha-methylacyl-CoA racemase deficiency.
Thompson SA, Calvin J, Hogg S, Ferdinandusse S, Wanders RJ, Barker RA.
Thompson SA, et al.
J Neurol Neurosurg Psychiatry. 2008 Apr;79(4):448-50. doi: 10.1136/jnnp.2007.129478. Epub 2007 Nov 21.
J Neurol Neurosurg Psychiatry. 2008.
PMID: 18032455
Item in Clipboard
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.
Clarke CE, et al.
Neurology. 2004 Jul 13;63(1):188-9. doi: 10.1212/01.wnl.0000132841.81250.b7.
Neurology. 2004.
PMID: 15249642
Review.
No abstract available.
Item in Clipboard
A new defect of peroxisomal function involving pristanic acid: a case report.
McLean BN, Allen J, Ferdinandusse S, Wanders RJ.
McLean BN, et al.
J Neurol Neurosurg Psychiatry. 2002 Mar;72(3):396-9. doi: 10.1136/jnnp.72.3.396.
J Neurol Neurosurg Psychiatry. 2002.
PMID: 11861706
Free PMC article.
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Mutations in the gene encoding peroxisomal alpha-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy.
Ferdinandusse S, Denis S, Clayton PT, Graham A, Rees JE, Allen JT, McLean BN, Brown AY, Vreken P, Waterham HR, Wanders RJ.
Ferdinandusse S, et al.
Nat Genet. 2000 Feb;24(2):188-91. doi: 10.1038/72861.
Nat Genet. 2000.
PMID: 10655068
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