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

Year Number of Results
1986 1
1997 1
1998 2
1999 2
2000 1
2001 4
2002 1
2003 7
2004 5
2005 5
2006 4
2007 6
2008 5
2009 7
2010 8
2011 8
2012 7
2014 1
2015 1
2018 1
2020 1
2021 1
2022 1
2023 1
2024 0

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76 results

Results by year

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Page 1
X-linked creatine transporter defect: an overview.
Salomons GS, van Dooren SJ, Verhoeven NM, Marsden D, Schwartz C, Cecil KM, DeGrauw TJ, Jakobs C. Salomons GS, et al. Among authors: degrauw tj. J Inherit Metab Dis. 2003;26(2-3):309-18. doi: 10.1023/a:1024405821638. J Inherit Metab Dis. 2003. PMID: 12889669 Review.
Congenital creatine transporter deficiency.
deGrauw TJ, Salomons GS, Cecil KM, Chuck G, Newmeyer A, Schapiro MB, Jakobs C. deGrauw TJ, et al. Neuropediatrics. 2002 Oct;33(5):232-8. doi: 10.1055/s-2002-36743. Neuropediatrics. 2002. PMID: 12536364
Language and social functioning in children and adolescents with epilepsy.
Byars AW, deGrauw TJ, Johnson CS, Perkins SM, Fastenau PS, Dunn DW, Austin JK. Byars AW, et al. Among authors: degrauw tj. Epilepsy Behav. 2014 Feb;31:167-71. doi: 10.1016/j.yebeh.2013.11.007. Epub 2014 Jan 14. Epilepsy Behav. 2014. PMID: 24434307 Free PMC article.
Neuromagnetic measures of word processing in bilinguals and monolinguals.
Wang Y, Xiang J, Vannest J, Holroyd T, Narmoneva D, Horn P, Liu Y, Rose D, deGrauw T, Holland S. Wang Y, et al. Among authors: degrauw t. Clin Neurophysiol. 2011 Sep;122(9):1706-17. doi: 10.1016/j.clinph.2011.02.008. Epub 2011 Mar 16. Clin Neurophysiol. 2011. PMID: 21414839
76 results