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

Year Number of Results
1967 1
1970 2
1971 5
1974 2
1975 2
1976 2
1977 5
1978 8
1979 2
1980 3
1981 6
1982 1
1983 3
1984 6
1985 5
1986 8
1987 7
1988 7
1989 6
1990 6
1991 5
1992 15
1993 7
1994 5
1995 6
1996 3
1997 6
1998 8
1999 3
2000 7
2001 8
2002 1
2003 4
2004 3
2006 7
2007 2
2008 4
2009 1
2011 1
2013 2
2014 1
2015 3
2016 1
2022 0
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Search Results

188 results
Results by year
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Page 1
Secondary mitochondrial pathology.
Sengers RC, Stadhouders AM. Sengers RC, et al. J Inherit Metab Dis. 1987;10 Suppl 1:98-104. doi: 10.1007/BF01812850. J Inherit Metab Dis. 1987. PMID: 2824922 Review.
Smith-Lemli-Opitz syndrome and the DHCR7 gene.
Jira PE, Waterham HR, Wanders RJ, Smeitink JA, Sengers RC, Wevers RA. Jira PE, et al. Among authors: sengers rc. Ann Hum Genet. 2003 May;67(Pt 3):269-80. doi: 10.1046/j.1469-1809.2003.00034.x. Ann Hum Genet. 2003. PMID: 12914579 Free article. Review.
Adenine nucleotide translocator 1 deficiency associated with Sengers syndrome.
Jordens EZ, Palmieri L, Huizing M, van den Heuvel LP, Sengers RC, Dörner A, Ruitenbeek W, Trijbels FJ, Valsson J, Sigfusson G, Palmieri F, Smeitink JA. Jordens EZ, et al. Among authors: sengers rc. Ann Neurol. 2002 Jul;52(1):95-9. doi: 10.1002/ana.10214. Ann Neurol. 2002. PMID: 12112053
[Mitochondrial defects].
Sengers RC, Stadhouders AM, Trijbels JM. Sengers RC, et al. Monatsschr Kinderheilkd. 1989 Jun;137(6):308-11. Monatsschr Kinderheilkd. 1989. PMID: 2668741 Review. German.
Multicore myopathy with restrictive cardiomyopathy.
Willemsen MA, van Oort AM, ter Laak HJ, Sengers RC, Gabreëls FJ. Willemsen MA, et al. Among authors: sengers rc. Acta Paediatr. 1997 Nov;86(11):1271-4. doi: 10.1111/j.1651-2227.1997.tb14862.x. Acta Paediatr. 1997. PMID: 9401528 Review.
Human NADH:ubiquinone oxidoreductase.
Smeitink J, Sengers R, Trijbels F, van den Heuvel L. Smeitink J, et al. Among authors: sengers r. J Bioenerg Biomembr. 2001 Jun;33(3):259-66. doi: 10.1023/a:1010743321800. J Bioenerg Biomembr. 2001. PMID: 11695836
Congenital muscular dystrophy.
Leyten QH, Gabreëls FJ, Renier WO, Ter Laak HJ, Sengers RC, Mullaart RA. Leyten QH, et al. Among authors: sengers rc. J Pediatr. 1989 Aug;115(2):214-21. doi: 10.1016/s0022-3476(89)80068-x. J Pediatr. 1989. PMID: 2754551
188 results