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

Year Number of Results
1972 1
1975 1
1976 1
1979 2
1984 2
1985 5
1988 2
1989 2
1990 4
1992 2
1993 3
1994 2
1995 1
1996 2
1997 1
1998 4
1999 7
2000 3
2001 5
2002 6
2003 1
2004 2
2005 2
2006 2
2007 3
2009 1
2013 1
2016 1
2024 0

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68 results

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Page 1
Inherited defects of biotin metabolism.
Baumgartner ER, Suormala T. Baumgartner ER, et al. Biofactors. 1999;10(2-3):287-90. doi: 10.1002/biof.5520100229. Biofactors. 1999. PMID: 10609895 Review. No abstract available.
Delayed-onset profound biotinidase deficiency.
Wolf B, Pomponio RJ, Norrgard KJ, Lott IT, Baumgartner ER, Suormala T, Ramaekers VT, Coskun T, Tokatli A, Ozalp I, Hymes J. Wolf B, et al. Among authors: baumgartner er. J Pediatr. 1998 Feb;132(2):362-5. doi: 10.1016/s0022-3476(98)70464-0. J Pediatr. 1998. PMID: 9506660
Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2.
Kennedy H, Haack TB, Hartill V, Mataković L, Baumgartner ER, Potter H, Mackay R, Alston CL, O'Sullivan S, McFarland R, Connolly G, Gannon C, King R, Mead S, Crozier I, Chan W, Florkowski CM, Sage M, Höfken T, Alhaddad B, Kremer LS, Kopajtich R, Feichtinger RG, Sperl W, Rodenburg RJ, Minet JC, Dobbie A, Strom TM, Meitinger T, George PM, Johnson CA, Taylor RW, Prokisch H, Doudney K, Mayr JA. Kennedy H, et al. Among authors: baumgartner er. Am J Hum Genet. 2016 Sep 1;99(3):674-682. doi: 10.1016/j.ajhg.2016.06.027. Epub 2016 Aug 11. Am J Hum Genet. 2016. PMID: 27523597 Free PMC article.
The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency.
Baumgartner MR, Almashanu S, Suormala T, Obie C, Cole RN, Packman S, Baumgartner ER, Valle D. Baumgartner MR, et al. Among authors: baumgartner er. J Clin Invest. 2001 Feb;107(4):495-504. doi: 10.1172/JCI11948. J Clin Invest. 2001. PMID: 11181649 Free PMC article.
Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.
Andresen BS, Olpin S, Poorthuis BJ, Scholte HR, Vianey-Saban C, Wanders R, Ijlst L, Morris A, Pourfarzam M, Bartlett K, Baumgartner ER, deKlerk JB, Schroeder LD, Corydon TJ, Lund H, Winter V, Bross P, Bolund L, Gregersen N. Andresen BS, et al. Among authors: baumgartner er. Am J Hum Genet. 1999 Feb;64(2):479-94. doi: 10.1086/302261. Am J Hum Genet. 1999. PMID: 9973285 Free PMC article.
Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy.
Van Hove JL, Van Damme-Lombaerts R, Grünewald S, Peters H, Van Damme B, Fryns JP, Arnout J, Wevers R, Baumgartner ER, Fowler B. Van Hove JL, et al. Among authors: baumgartner er. Am J Med Genet. 2002 Aug 1;111(2):195-201. doi: 10.1002/ajmg.10499. Am J Med Genet. 2002. PMID: 12210350
68 results