Similar articles for PMID: 17372139

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1

Phenotypes of female adrenoleukodystrophy.

Jung HH, Wimplinger I, Jung S, Landau K, Gal A, Heppner FL. Jung HH, et al. Neurology. 2007 Mar 20;68(12):960-1. doi: 10.1212/01.wnl.0000257129.51273.73. Neurology. 2007. PMID: 17372139 No abstract available.

2

Spinocerebellar variant of adrenoleukodystrophy with a novel ABCD1 gene mutation.

Li JY, Hsu CC, Tsai CR. Li JY, et al. J Neurol Sci. 2010 Mar 15;290(1-2):163-5. doi: 10.1016/j.jns.2009.12.002. Epub 2009 Dec 29. J Neurol Sci. 2010. PMID: 20042197

3

Oligosymptomatic adrenomyeloneuropathy due to a novel mutation in the ABCD1 start codon.

Dunkl V, Rau I, Wunderlich G, Fink GR, Lehmann HC. Dunkl V, et al. J Neurol Sci. 2016 Aug 15;367:81-2. doi: 10.1016/j.jns.2016.05.047. Epub 2016 May 24. J Neurol Sci. 2016. PMID: 27423567 No abstract available.

4

X-linked adrenoleukodystrophy in women: a cross-sectional cohort study.

Engelen M, Barbier M, Dijkstra IM, Schür R, de Bie RM, Verhamme C, Dijkgraaf MG, Aubourg PA, Wanders RJ, van Geel BM, de Visser M, Poll-The BT, Kemp S. Engelen M, et al. Brain. 2014 Mar;137(Pt 3):693-706. doi: 10.1093/brain/awt361. Epub 2014 Jan 29. Brain. 2014. PMID: 24480483

5

X-linked adrenoleukodystrophy presenting as isolated spastic paraparesia.

Unluturk Z, Erdogan Ç, Tekin S. Unluturk Z, et al. Acta Neurol Belg. 2019 Dec;119(4):631-632. doi: 10.1007/s13760-019-01085-8. Epub 2019 Jan 30. Acta Neurol Belg. 2019. PMID: 30697666 No abstract available.

6

Adult onset cerebral form of X-linked adrenoleukodystrophy with dementia of frontal lobe type with new L160P mutation in ABCD1 gene.

Sutovský S, Petrovic R, Chandoga J, Turcáni P. Sutovský S, et al. J Neurol Sci. 2007 Dec 15;263(1-2):149-53. doi: 10.1016/j.jns.2007.01.082. Epub 2007 Jul 26. J Neurol Sci. 2007. PMID: 17662307

7

Adult-onset cerebello-brainstem dominant form of X-linked adrenoleukodystrophy presenting as multiple system atrophy: case report and literature review.

Ogaki K, Koga S, Aoki N, Lin W, Suzuki K, Ross OA, Dickson DW. Ogaki K, et al. Neuropathology. 2016 Feb;36(1):64-76. doi: 10.1111/neup.12230. Epub 2015 Jul 31. Neuropathology. 2016. PMID: 26227820 Free PMC article.

8

Adrenomyeloneuropathy due to mutation in the ABCD1 gene as underlying factor in spastic paraparesis.

Ylikallio E, Rahikkala E, Keski-Filppula R, Auranen M, Tyynismaa H. Ylikallio E, et al. Duodecim. 2017;133(7):683-7. Duodecim. 2017. PMID: 29243459

9

X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype.

Maier EM, Mayerhofer PU, Asheuer M, Köhler W, Rothe M, Muntau AC, Roscher AA, Holzinger A, Aubourg P, Berger J. Maier EM, et al. Biochem Biophys Res Commun. 2008 Dec 5;377(1):176-80. doi: 10.1016/j.bbrc.2008.09.092. Epub 2008 Oct 1. Biochem Biophys Res Commun. 2008. PMID: 18834860

10

X-linked adrenoleukodystrophy: clinical, metabolic, genetic and pathophysiological aspects.

Kemp S, Berger J, Aubourg P. Kemp S, et al. Biochim Biophys Acta. 2012 Sep;1822(9):1465-74. doi: 10.1016/j.bbadis.2012.03.012. Epub 2012 Mar 28. Biochim Biophys Acta. 2012. PMID: 22483867 Free article. Review.

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