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

Year Number of Results
1946 2
1947 3
1948 1
1949 1
1957 1
1958 2
1960 2
1961 1
1962 3
1964 2
1965 2
1966 3
1967 5
1968 3
1969 9
1970 7
1971 6
1972 7
1973 6
1974 3
1975 2
1976 2
1977 7
1978 10
1979 3
1980 8
1981 4
1982 5
1983 7
1984 6
1985 7
1986 7
1987 11
1988 7
1989 6
1990 12
1991 9
1992 11
1993 18
1994 12
1995 16
1996 7
1997 17
1998 7
1999 17
2000 15
2001 20
2002 15
2003 11
2004 7
2005 18
2006 16
2007 13
2008 6
2009 11
2010 12
2011 15
2012 19
2013 11
2014 7
2015 11
2016 12
2017 13
2018 7
2019 12
2020 16
2021 7
2022 10
Text availability
Article attribute
Article type
Publication date

Search Results

541 results
Results by year
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Page 1
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. Among authors: raymond gv. 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.
X-Linked Adrenoleukodystrophy.
Raymond GV, Moser AB, Fatemi A. Raymond GV, et al. 1999 Mar 26 [updated 2018 Feb 15]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 1999 Mar 26 [updated 2018 Feb 15]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301491 Free Books & Documents. Review.
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: raymond gv. 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.
Leukodystrophy: Basic and Clinical.
Raymond GV. Raymond GV. Adv Neurobiol. 2017;15:365-382. doi: 10.1007/978-3-319-57193-5_14. Adv Neurobiol. 2017. PMID: 28674989 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: raymond gv. 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.
Child neurology: Zellweger syndrome.
Lee PR, Raymond GV. Lee PR, et al. Among authors: raymond gv. Neurology. 2013 May 14;80(20):e207-10. doi: 10.1212/WNL.0b013e3182929f8e. Neurology. 2013. PMID: 23671347 Free PMC article. Review.
X-linked adrenoleukodystrophy.
Moser HW, Mahmood A, Raymond GV. Moser HW, et al. Among authors: raymond gv. Nat Clin Pract Neurol. 2007 Mar;3(3):140-51. doi: 10.1038/ncpneuro0421. Nat Clin Pract Neurol. 2007. PMID: 17342190 Review.
Peroxisomal disorders.
Raymond GV. Raymond GV. Curr Opin Pediatr. 1999 Dec;11(6):572-6. doi: 10.1097/00008480-199912000-00017. Curr Opin Pediatr. 1999. PMID: 10590918 Review.
541 results