Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 157

1.

Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.

Corzo D, Gibson W, Johnson K, Mitchell G, LePage G, Cox GF, Casey R, Zeiss C, Tyson H, Cutting GR, Raymond GV, Smith KD, Watkins PA, Moser AB, Moser HW, Steinberg SJ.

Am J Hum Genet. 2002 Jun;70(6):1520-31. Epub 2002 Apr 29.

PMID:
11992258
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

[X-linked adrenoleukodystrophy].

Aubourg P.

Ann Endocrinol (Paris). 2007 Dec;68(6):403-11. Epub 2007 May 29. Review. French.

PMID:
17532287
[PubMed - indexed for MEDLINE]
3.

Clinical and genetic aspects of X-linked adrenoleukodystrophy.

Gärtner J, Braun A, Holzinger A, Roerig P, Lenard HG, Roscher AA.

Neuropediatrics. 1998 Feb;29(1):3-13. Review.

PMID:
9553942
[PubMed - indexed for MEDLINE]
4.

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

Kemp S, Berger J, Aubourg P.

Biochim Biophys Acta. 2012 Sep;1822(9):1465-74. doi: 10.1016/j.bbadis.2012.03.012. Epub 2012 Mar 28. Review.

PMID:
22483867
[PubMed - indexed for MEDLINE]
Free Article
5.

ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations.

Kemp S, Pujol A, Waterham HR, van Geel BM, Boehm CD, Raymond GV, Cutting GR, Wanders RJ, Moser HW.

Hum Mutat. 2001 Dec;18(6):499-515. Review.

PMID:
11748843
[PubMed - indexed for MEDLINE]
6.

X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment.

Kemp S, Wanders RJ.

Mol Genet Metab. 2007 Mar;90(3):268-76. Epub 2006 Nov 7. Review.

PMID:
17092750
[PubMed - indexed for MEDLINE]
7.

[Adrenoleukodystrophy: molecular pathogenesis and development of therapeutic agents].

Morita M.

Yakugaku Zasshi. 2007 Jul;127(7):1059-64. Review. Japanese.

PMID:
17603264
[PubMed - indexed for MEDLINE]
Free Article
8.

[Adrenoleukodystrophy: structure and function of ALDP, and intracellular behavior of mutant ALDP with naturally occurring missense mutations].

Takahashi N, Morita M, Imanaka T.

Yakugaku Zasshi. 2007 Jan;127(1):163-72. Review. Japanese.

PMID:
17202797
[PubMed - indexed for MEDLINE]
Free Article
9.

Biochemical aspects of X-linked adrenoleukodystrophy.

Kemp S, Wanders R.

Brain Pathol. 2010 Jul;20(4):831-7. doi: 10.1111/j.1750-3639.2010.00391.x. Review.

PMID:
20626744
[PubMed - indexed for MEDLINE]
10.

Cerebral inflammation in X-linked adrenoleukodystrophy.

McGuinness MC, Smith KD.

Arch Immunol Ther Exp (Warsz). 1999;47(5):281-7. Review.

PMID:
10604233
[PubMed - indexed for MEDLINE]
11.

Adrenoleukodystrophy.

Cappa M, Bizzarri C, Vollono C, Petroni A, Banni S.

Endocr Dev. 2011;20:149-60. doi: 10.1159/000321236. Epub 2010 Dec 16. Review.

PMID:
21164268
[PubMed - indexed for MEDLINE]
12.

Adrenoleukodystrophy gene: unexpected homology to a protein involved in peroxisome biogenesis.

Aubourg P, Mosser J, Douar AM, Sarde CO, Lopez J, Mandel JL.

Biochimie. 1993;75(3-4):293-302. Review.

PMID:
8507690
[PubMed - indexed for MEDLINE]
13.

[Peroxisomal ABC transporters and X-linked adrenoleukodystrophy].

Geillon F, Trompier D, Gondcaille C, Lizard G, Savary S.

Med Sci (Paris). 2012 Dec;28(12):1087-94. doi: 10.1051/medsci/20122812019. Epub 2012 Dec 21. Review. French.

PMID:
23290409
[PubMed - indexed for MEDLINE]
14.

The neurobiology of X-linked adrenoleukodystrophy, a demyelinating peroxisomal disorder.

Dubois-Dalcq M, Feigenbaum V, Aubourg P.

Trends Neurosci. 1999 Jan;22(1):4-12. Review.

PMID:
10088993
[PubMed - indexed for MEDLINE]
15.

X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.

Berger J, Gärtner J.

Biochim Biophys Acta. 2006 Dec;1763(12):1721-32. Epub 2006 Jul 26. Review.

PMID:
16949688
[PubMed - indexed for MEDLINE]
Free Article
16.

DNA diagnosis of X-linked adrenoleukodystrophy.

Seneca S, Lissens W.

J Inherit Metab Dis. 1995;18 Suppl 1:34-44. Review.

PMID:
9053554
[PubMed - indexed for MEDLINE]
17.

X-linked adrenoleukodystrophy: genes, mutations, and phenotypes.

Smith KD, Kemp S, Braiterman LT, Lu JF, Wei HM, Geraghty M, Stetten G, Bergin JS, Pevsner J, Watkins PA.

Neurochem Res. 1999 Apr;24(4):521-35. Review.

PMID:
10227685
[PubMed - indexed for MEDLINE]
18.

ABC subfamily D proteins and very long chain fatty acid metabolism as novel targets in adrenoleukodystrophy.

Morita M, Shimozawa N, Kashiwayama Y, Suzuki Y, Imanaka T.

Curr Drug Targets. 2011 May;12(5):694-706. Review.

PMID:
21039332
[PubMed - indexed for MEDLINE]
19.

Adrenoleukodystrophy and other peroxisomal diseases.

Aubourg P.

Curr Opin Genet Dev. 1994 Jun;4(3):407-11. Review.

PMID:
7919919
[PubMed - indexed for MEDLINE]
20.

General aspects and neuropathology of X-linked adrenoleukodystrophy.

Ferrer I, Aubourg P, Pujol A.

Brain Pathol. 2010 Jul;20(4):817-30. doi: 10.1111/j.1750-3639.2010.00390.x. Review.

PMID:
20626743
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk