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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 2
1999 1
2002 3
2003 3
2005 3
2006 3
2007 4
2008 3
2009 2
2010 2
2011 3
2012 3
2013 5
2014 9
2015 7
2016 5
2017 5
2018 4
2019 2
2020 3
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60 results
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Page 1
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines.
Braverman NE, Raymond GV, Rizzo WB, Moser AB, Wilkinson ME, Stone EM, Steinberg SJ, Wangler MF, Rush ET, Hacia JG, Bose M. Braverman NE, et al. Among authors: Moser AB. Mol Genet Metab. 2016 Mar;117(3):313-21. doi: 10.1016/j.ymgme.2015.12.009. Epub 2015 Dec 23. Mol Genet Metab. 2016. PMID: 26750748 Free PMC article. Review.
Therapeutic strategies in adrenoleukodystrophy.
Turk BR, Moser AB, Fatemi A. Turk BR, et al. Among authors: Moser AB. Wien Med Wochenschr. 2017 Jun;167(9-10):219-226. doi: 10.1007/s10354-016-0534-2. Epub 2017 May 10. Wien Med Wochenschr. 2017. PMID: 28493141 Review. English.
Zellweger Spectrum Disorder.
Steinberg SJ, Raymond GV, Braverman NE, Moser AB. Steinberg SJ, et al. Among authors: Moser AB. 2003 Dec 12 [updated 2017 Dec 21]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301621 Free Books & Documents. Review.
Hif-2α promotes degradation of mammalian peroxisomes by selective autophagy.
Walter KM, Schönenberger MJ, Trötzmüller M, Horn M, Elsässer HP, Moser AB, Lucas MS, Schwarz T, Gerber PA, Faust PL, Moch H, Köfeler HC, Krek W, Kovacs WJ. Walter KM, et al. Among authors: Moser AB. Cell Metab. 2014 Nov 4;20(5):882-897. doi: 10.1016/j.cmet.2014.09.017. Epub 2014 Nov 4. Cell Metab. 2014. PMID: 25440060 Free article.
X-Linked Adrenoleukodystrophy.
Raymond GV, Moser AB, Fatemi A. Raymond GV, et al. Among authors: Moser AB. 1999 Mar 26 [updated 2018 Feb 15]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301491 Free Books & Documents. Review.
A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkers.
Wangler MF, Hubert L, Donti TR, Ventura MJ, Miller MJ, Braverman N, Gawron K, Bose M, Moser AB, Jones RO, Rizzo WB, Sutton VR, Sun Q, Kennedy AD, Elsea SH. Wangler MF, et al. Among authors: Moser AB. Genet Med. 2018 Oct;20(10):1274-1283. doi: 10.1038/gim.2017.262. Epub 2018 Feb 8. Genet Med. 2018. PMID: 29419819
Brain endothelial dysfunction in cerebral adrenoleukodystrophy.
Musolino PL, Gong Y, Snyder JM, Jimenez S, Lok J, Lo EH, Moser AB, Grabowski EF, Frosch MP, Eichler FS. Musolino PL, et al. Among authors: Moser AB. Brain. 2015 Nov;138(Pt 11):3206-20. doi: 10.1093/brain/awv250. Epub 2015 Sep 15. Brain. 2015. PMID: 26377633 Free PMC article.
Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder.
Falkenberg KD, Braverman NE, Moser AB, Steinberg SJ, Klouwer FCC, Schlüter A, Ruiz M, Pujol A, Engvall M, Naess K, van Spronsen F, Körver-Keularts I, Rubio-Gozalbo ME, Ferdinandusse S, Wanders RJA, Waterham HR. Falkenberg KD, et al. Among authors: Moser AB. Am J Hum Genet. 2017 Dec 7;101(6):965-976. doi: 10.1016/j.ajhg.2017.11.007. Am J Hum Genet. 2017. PMID: 29220678 Free PMC article.
A model-based approach to assess the exposure-response relationship of Lorenzo's oil in adrenoleukodystrophy.
Ahmed MA, Kartha RV, Brundage RC, Cloyd J, Basu C, Carlin BP, Jones RO, Moser AB, Fatemi A, Raymond GV. Ahmed MA, et al. Among authors: Moser AB. Br J Clin Pharmacol. 2016 Jun;81(6):1058-66. doi: 10.1111/bcp.12897. Epub 2016 Apr 3. Br J Clin Pharmacol. 2016. PMID: 26836218 Free PMC article. Clinical Trial.
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