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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 7
2009 11
2010 13
2011 17
2012 19
2013 11
2014 8
2015 11
2016 12
2017 13
2018 6
2019 12
2020 16
2021 7
2022 12
2023 5
2024 5

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557 results

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Page 1
Showing results for raymond g
Search for Raymon G instead (2 results)
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.
Zellweger Spectrum Disorder.
Steinberg SJ, Raymond GV, Braverman NE, Moser AB. Steinberg SJ, et al. Among authors: raymond gv. 2003 Dec 12 [updated 2020 Oct 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2003 Dec 12 [updated 2020 Oct 29]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301621 Free Books & Documents. Review.
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: raymond gv. Neurology. 2022 Nov 22;99(21):940-951. doi: 10.1212/WNL.0000000000201374. Epub 2022 Sep 29. Neurology. 2022. PMID: 36175155 Free PMC article.
X-Linked Adrenoleukodystrophy.
Raymond GV, Moser AB, Fatemi A. Raymond GV, et al. 1999 Mar 26 [updated 2023 Apr 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, 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, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301491 Free Books & Documents. 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.
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.
Peroxisome biogenesis disorders.
Steinberg SJ, Dodt G, Raymond GV, Braverman NE, Moser AB, Moser HW. Steinberg SJ, et al. Among authors: raymond gv. Biochim Biophys Acta. 2006 Dec;1763(12):1733-48. doi: 10.1016/j.bbamcr.2006.09.010. Epub 2006 Sep 14. Biochim Biophys Acta. 2006. PMID: 17055079 Free article. Review.
557 results