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

Year Number of Results
1950 1
1951 1
1952 1
1953 1
1969 1
1987 1
1988 1
1994 1
1996 2
1997 1
1998 3
1999 3
2000 2
2001 2
2002 4
2004 2
2005 1
2006 3
2007 4
2008 6
2009 6
2010 5
2011 5
2012 5
2013 1
2014 4
2015 10
2016 6
2017 6
2018 6
2019 10
2020 7
2021 14
2022 1
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Search Results

119 results
Results by year
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Page 1
Pathophysiology of X-linked adrenoleukodystrophy.
Berger J, Forss-Petter S, Eichler FS. Berger J, et al. Among authors: eichler fs. Biochimie. 2014 Mar;98(100):135-42. doi: 10.1016/j.biochi.2013.11.023. Epub 2013 Dec 4. Biochimie. 2014. PMID: 24316281 Free PMC article. Review.
The Changing Face of Adrenoleukodystrophy.
Zhu J, Eichler F, Biffi A, Duncan CN, Williams DA, Majzoub JA. Zhu J, et al. Among authors: eichler f. Endocr Rev. 2020 Aug 1;41(4):577-93. doi: 10.1210/endrev/bnaa013. Endocr Rev. 2020. PMID: 32364223 Free PMC article. Review.
Hematopoietic Stem-Cell Gene Therapy for Cerebral Adrenoleukodystrophy.
Eichler F, Duncan C, Musolino PL, Orchard PJ, De Oliveira S, Thrasher AJ, Armant M, Dansereau C, Lund TC, Miller WP, Raymond GV, Sankar R, Shah AJ, Sevin C, Gaspar HB, Gissen P, Amartino H, Bratkovic D, Smith NJC, Paker AM, Shamir E, O'Meara T, Davidson D, Aubourg P, Williams DA. Eichler F, et al. N Engl J Med. 2017 Oct 26;377(17):1630-1638. doi: 10.1056/NEJMoa1700554. Epub 2017 Oct 4. N Engl J Med. 2017. PMID: 28976817 Free PMC article. Clinical Trial.
Case definition and classification of leukodystrophies and leukoencephalopathies.
Vanderver A, Prust M, Tonduti D, Mochel F, Hussey HM, Helman G, Garbern J, Eichler F, Labauge P, Aubourg P, Rodriguez D, Patterson MC, Van Hove JL, Schmidt J, Wolf NI, Boespflug-Tanguy O, Schiffmann R, van der Knaap MS; GLIA Consortium. Vanderver A, et al. Among authors: eichler f. Mol Genet Metab. 2015 Apr;114(4):494-500. doi: 10.1016/j.ymgme.2015.01.006. Epub 2015 Jan 29. Mol Genet Metab. 2015. PMID: 25649058 Free PMC article. Review.
MRI surveillance of boys with X-linked adrenoleukodystrophy identified by newborn screening: Meta-analysis and consensus guidelines.
Mallack EJ, Turk BR, Yan H, Price C, Demetres M, Moser AB, Becker C, Hollandsworth K, Adang L, Vanderver A, Van Haren K, Ruzhnikov M, Kurtzberg J, Maegawa G, Orchard PJ, Lund TC, Raymond GV, Regelmann M, Orsini JJ, Seeger E, Kemp S, Eichler F, Fatemi A. Mallack EJ, et al. Among authors: eichler f. J Inherit Metab Dis. 2021 May;44(3):728-739. doi: 10.1002/jimd.12356. Epub 2021 Jan 9. J Inherit Metab Dis. 2021. PMID: 33373467 Free PMC article.
Endocrine dysfunction in adrenoleukodystrophy.
Engelen M, Kemp S, Eichler F. Engelen M, et al. Among authors: eichler f. Handb Clin Neurol. 2021;182:257-267. doi: 10.1016/B978-0-12-819973-2.00018-6. Handb Clin Neurol. 2021. PMID: 34266597 Review.
Immune response in leukodystrophies.
Eichler F, Van Haren K. Eichler F, et al. Pediatr Neurol. 2007 Oct;37(4):235-44. doi: 10.1016/j.pediatrneurol.2007.06.011. Pediatr Neurol. 2007. PMID: 17903666 Review.
Inherited or acquired metabolic disorders.
Eichler F, Ratai E, Carroll JJ, Masdeu JC. Eichler F, et al. Handb Clin Neurol. 2016;135:603-636. doi: 10.1016/B978-0-444-53485-9.00029-5. Handb Clin Neurol. 2016. PMID: 27432685 Review.
Practical Approaches and Knowledge Gaps in the Care for Children With Leukodystrophies.
Keller SR, Mallack EJ, Rubin JP, Accardo JA, Brault JA, Corre CS, Elizondo C, Garafola J, Jackson-Garcia AC, Rhee J, Seeger E, Shullanberger KC, Tourjee A, Trovato MK, Waldman AT, Wallace JL, Wallace MR, Werner K, White A, Ess KC, Becker C, Eichler FS. Keller SR, et al. Among authors: eichler fs. J Child Neurol. 2021 Jan;36(1):65-78. doi: 10.1177/0883073820946154. Epub 2020 Sep 2. J Child Neurol. 2021. PMID: 32875938 Free PMC article. Review.
Unusual Behaviors in a 7-year-old Boy.
Chang L, Shao DD, Eichler FS, Srivastava S. Chang L, et al. Among authors: eichler fs. Pediatr Rev. 2021 Jan;42(Suppl 1):S122-S125. doi: 10.1542/pir.2019-0244. Pediatr Rev. 2021. PMID: 33386381 No abstract available.
119 results