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

Year Number of Results
1971 1
1973 1
1975 1
1976 2
1978 3
1980 2
1981 6
1982 4
1983 2
1984 1
1985 1
1986 1
1987 2
1989 2
1990 3
1991 10
1992 3
1993 5
1994 5
1995 5
1996 7
1997 3
1998 4
1999 3
2000 3
2001 5
2002 3
2003 7
2004 1
2005 2
2006 5
2007 4
2009 1
2010 1
2011 1
2021 1
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110 results
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Page 1
Disorders of the pyruvate dehydrogenase complex.
Stansbie D, Wallace SJ, Marsac C. Stansbie D, et al. Among authors: marsac c. J Inherit Metab Dis. 1986;9(2):105-19. doi: 10.1007/BF01799447. J Inherit Metab Dis. 1986. PMID: 3018357 Review.
[Enzymopathic congenital hyperlactacidemia].
Leroux JP, Marsac C, Saudubray JM. Leroux JP, et al. Among authors: marsac c. Ann Biol Clin (Paris). 1976;34(2):151-9. Ann Biol Clin (Paris). 1976. PMID: 184725 Review. French.
Homozygous deletion in the coding sequence of the c-mer gene in RCS rats unravels general mechanisms of physiological cell adhesion and apoptosis.
Nandrot E, Dufour EM, Provost AC, Péquignot MO, Bonnel S, Gogat K, Marchant D, Rouillac C, Sépulchre de Condé B, Bihoreau MT, Shaver C, Dufier JL, Marsac C, Lathrop M, Menasche M, Abitbol MM. Nandrot E, et al. Among authors: marsac c. Neurobiol Dis. 2000 Dec;7(6 Pt B):586-99. doi: 10.1006/nbdi.2000.0328. Neurobiol Dis. 2000. PMID: 11114258
Eight previously unidentified mutations found in the OA1 ocular albinism gene.
Mayeur H, Roche O, Vêtu C, Jaliffa C, Marchant D, Dollfus H, Bonneau D, Munier FL, Schorderet DF, Levin AV, Héon E, Sutherland J, Lacombe D, Said E, Mezer E, Kaplan J, Dufier JL, Marsac C, Menasche M, Abitbol M. Mayeur H, et al. Among authors: marsac c. BMC Med Genet. 2006 Apr 28;7:41. doi: 10.1186/1471-2350-7-41. BMC Med Genet. 2006. PMID: 16646960 Free PMC article.
110 results
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