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Results by year

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

Year Number of Results
1952 2
1953 1
1954 1
1955 1
1957 1
1964 1
1966 1
1967 3
1970 1
1971 1
1972 1
1974 1
1976 2
1978 4
1979 3
1980 4
1981 5
1982 9
1983 9
1984 12
1985 12
1986 9
1987 10
1988 10
1989 13
1990 22
1991 9
1992 16
1993 24
1994 18
1995 28
1996 20
1997 17
1998 18
1999 25
2000 26
2001 26
2002 20
2003 22
2004 18
2005 30
2006 31
2007 30
2008 36
2009 28
2010 41
2011 38
2012 37
2013 42
2014 47
2015 51
2016 52
2017 44
2018 41
2019 26
2020 44
2021 64
2022 52
2023 44
2024 22

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1,115 results

Results by year

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Page 1
International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy: A Consensus-Based Approach.
Engelen M, van Ballegoij WJC, Mallack EJ, Van Haren KP, Köhler W, Salsano E, van Trotsenburg ASP, Mochel F, Sevin C, Regelmann MO, Tritos NA, Halper A, Lachmann RH, Davison J, Raymond GV, Lund TC, Orchard PJ, Kuehl JS, Lindemans CA, Caruso P, Turk BR, Moser AB, Vaz FM, Ferdinandusse S, Kemp S, Fatemi A, Eichler FS, Huffnagel IC. Engelen M, et al. Among authors: moser ab. Neurology. 2022 Nov 22;99(21):940-951. doi: 10.1212/WNL.0000000000201374. Epub 2022 Sep 29. Neurology. 2022. PMID: 36175155 Free PMC article.
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.
Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms.
Chung HL, Wangler MF, Marcogliese PC, Jo J, Ravenscroft TA, Zuo Z, Duraine L, Sadeghzadeh S, Li-Kroeger D, Schmidt RE, Pestronk A, Rosenfeld JA, Burrage L, Herndon MJ, Chen S; Members of Undiagnosed Diseases Network; Shillington A, Vawter-Lee M, Hopkin R, Rodriguez-Smith J, Henrickson M, Lee B, Moser AB, Jones RO, Watkins P, Yoo T, Mar S, Choi M, Bucelli RC, Yamamoto S, Lee HK, Prada CE, Chae JH, Vogel TP, Bellen HJ. Chung HL, et al. Among authors: moser ab. Neuron. 2020 May 20;106(4):589-606.e6. doi: 10.1016/j.neuron.2020.02.021. Epub 2020 Mar 12. Neuron. 2020. PMID: 32169171 Free PMC article.
X-Linked Adrenoleukodystrophy.
Raymond GV, Moser AB, Fatemi A. Raymond GV, et al. Among authors: moser ab. 1999 Mar 26 [updated 2023 Apr 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 1999 Mar 26 [updated 2023 Apr 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301491 Free Books & Documents. Review.
The authors reply.
Pölkki A, Moser A, Raj R, Takala J, Bendel S, Jakob SM, Reinikainen M. Pölkki A, et al. Among authors: moser a. Crit Care Med. 2024 Apr 1;52(4):e217-e218. doi: 10.1097/CCM.0000000000006205. Epub 2024 Mar 14. Crit Care Med. 2024. PMID: 38483239 No abstract available.
1,115 results