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

Year Number of Results
1968 1
1970 1
1971 1
1972 1
1975 1
1980 1
1982 6
1984 1
1985 4
1986 1
1987 4
1988 2
1989 9
1990 7
1991 4
1992 12
1993 4
1994 3
1995 12
1996 8
1997 6
1998 5
1999 6
2000 5
2001 5
2002 1
2003 5
2004 5
2005 6
2006 4
2007 3
2008 1
2009 6
2010 6
2011 2
2012 4
2013 3
2014 1
2015 4
2016 1
2021 1
2024 0

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156 results

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Page 1
Nontransplant treatment of tyrosinemia.
Holme E, Lindstedt S. Holme E, et al. Clin Liver Dis. 2000 Nov;4(4):805-14. doi: 10.1016/s1089-3261(05)70142-2. Clin Liver Dis. 2000. PMID: 11232358 Review.
Diagnosis and management of tyrosinemia type I.
Holme E, Lindstedt S. Holme E, et al. Curr Opin Pediatr. 1995 Dec;7(6):726-32. doi: 10.1097/00008480-199512000-00017. Curr Opin Pediatr. 1995. PMID: 8776026 Review.
Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency.
Van Kuilenburg AB, Vreken P, Abeling NG, Bakker HD, Meinsma R, Van Lenthe H, De Abreu RA, Smeitink JA, Kayserili H, Apak MY, Christensen E, Holopainen I, Pulkki K, Riva D, Botteon G, Holme E, Tulinius M, Kleijer WJ, Beemer FA, Duran M, Niezen-Koning KE, Smit GP, Jakobs C, Smit LM, Van Gennip AH, et al. Van Kuilenburg AB, et al. Among authors: holme e. Hum Genet. 1999 Jan;104(1):1-9. doi: 10.1007/pl00008711. Hum Genet. 1999. PMID: 10071185 Review.
Superoxide dismutase in extracellular fluids.
Marklund SL, Holme E, Hellner L. Marklund SL, et al. Among authors: holme e. Clin Chim Acta. 1982 Nov 24;126(1):41-51. doi: 10.1016/0009-8981(82)90360-6. Clin Chim Acta. 1982. PMID: 7172448
Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.
Burda P, Kuster A, Hjalmarson O, Suormala T, Bürer C, Lutz S, Roussey G, Christa L, Asin-Cayuela J, Kollberg G, Andersson BA, Watkins D, Rosenblatt DS, Fowler B, Holme E, Froese DS, Baumgartner MR. Burda P, et al. Among authors: holme e. J Inherit Metab Dis. 2015 Sep;38(5):863-72. doi: 10.1007/s10545-015-9810-3. Epub 2015 Jan 30. J Inherit Metab Dis. 2015. PMID: 25633902 Free article. Review.
Complement activation in Henoch-Schönlein purpura.
Smith GC, Davidson JE, Hughes DA, Holme E, Beattie TJ. Smith GC, et al. Among authors: holme e. Pediatr Nephrol. 1997 Aug;11(4):477-80. doi: 10.1007/s004670050320. Pediatr Nephrol. 1997. PMID: 9260249
156 results