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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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2008 | 1 |
2009 | 1 |
2010 | 1 |
2011 | 1 |
2012 | 1 |
2024 | 0 |
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Page 1
Hypoperfusion predicts lesion progression in cerebral X-linked adrenoleukodystrophy.
Brain. 2012 Sep;135(Pt 9):2676-83. doi: 10.1093/brain/aws206.
Brain. 2012.
PMID: 22961546
Free PMC article.
Oral L-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1.
Garofalo K, Penno A, Schmidt BP, Lee HJ, Frosch MP, von Eckardstein A, Brown RH, Hornemann T, Eichler FS.
Garofalo K, et al.
J Clin Invest. 2011 Dec;121(12):4735-45. doi: 10.1172/JCI57549.
J Clin Invest. 2011.
PMID: 22045570
Free PMC article.
Clinical Trial.
Item in Clipboard
Hereditary sensory neuropathy type 1 is caused by the accumulation of two neurotoxic sphingolipids.
Penno A, Reilly MM, Houlden H, Laurá M, Rentsch K, Niederkofler V, Stoeckli ET, Nicholson G, Eichler F, Brown RH Jr, von Eckardstein A, Hornemann T.
Penno A, et al.
J Biol Chem. 2010 Apr 9;285(15):11178-87. doi: 10.1074/jbc.M109.092973. Epub 2010 Jan 22.
J Biol Chem. 2010.
PMID: 20097765
Free PMC article.
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Overexpression of the wild-type SPT1 subunit lowers desoxysphingolipid levels and rescues the phenotype of HSAN1.
Eichler FS, Hornemann T, McCampbell A, Kuljis D, Penno A, Vardeh D, Tamrazian E, Garofalo K, Lee HJ, Kini L, Selig M, Frosch M, Gable K, von Eckardstein A, Woolf CJ, Guan G, Harmon JM, Dunn TM, Brown RH Jr.
Eichler FS, et al.
J Neurosci. 2009 Nov 18;29(46):14646-51. doi: 10.1523/JNEUROSCI.2536-09.2009.
J Neurosci. 2009.
PMID: 19923297
Free PMC article.
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Seven-Tesla proton magnetic resonance spectroscopic imaging in adult X-linked adrenoleukodystrophy.
Ratai E, Kok T, Wiggins C, Wiggins G, Grant E, Gagoski B, O'Neill G, Adalsteinsson E, Eichler F.
Ratai E, et al.
Arch Neurol. 2008 Nov;65(11):1488-94. doi: 10.1001/archneur.65.11.1488.
Arch Neurol. 2008.
PMID: 19001168
Free PMC article.
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