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

Year Number of Results
1978 1
1980 1
1982 1
1985 1
1986 5
1987 3
1988 4
1989 3
1990 4
1991 5
1992 5
1993 6
1994 5
1995 4
1996 8
1997 4
1998 10
1999 4
2000 4
2001 7
2002 5
2003 9
2004 5
2005 6
2006 4
2007 5
2008 4
2009 6
2010 5
2011 4
2012 11
2013 8
2014 5
2015 9
2016 10
2017 7
2018 1
2019 7
2020 6
2021 4
2022 1
Text availability
Article attribute
Article type
Publication date

Search Results

185 results
Results by year
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Page 1
Disorders affecting vitamin B6 metabolism.
Wilson MP, Plecko B, Mills PB, Clayton PT. Wilson MP, et al. Among authors: clayton pt. J Inherit Metab Dis. 2019 Jul;42(4):629-646. doi: 10.1002/jimd.12060. Epub 2019 Mar 20. J Inherit Metab Dis. 2019. PMID: 30671974 Review.
Consensus guidelines for the diagnosis and management of pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde dehydrogenase deficiency.
Coughlin CR 2nd, Tseng LA, Abdenur JE, Ashmore C, Boemer F, Bok LA, Boyer M, Buhas D, Clayton PT, Das A, Dekker H, Evangeliou A, Feillet F, Footitt EJ, Gospe SM Jr, Hartmann H, Kara M, Kristensen E, Lee J, Lilje R, Longo N, Lunsing RJ, Mills P, Papadopoulou MT, Pearl PL, Piazzon F, Plecko B, Saini AG, Santra S, Sjarif DR, Stockler-Ipsiroglu S, Striano P, Van Hove JLK, Verhoeven-Duif NM, Wijburg FA, Zuberi SM, van Karnebeek CDM. Coughlin CR 2nd, et al. Among authors: clayton pt. J Inherit Metab Dis. 2021 Jan;44(1):178-192. doi: 10.1002/jimd.12332. Epub 2020 Dec 1. J Inherit Metab Dis. 2021. PMID: 33200442
SLC39A14 Deficiency.
Tuschl K, Gregory A, Meyer E, Clayton PT, Hayflick SJ, Mills PB, Kurian MA. Tuschl K, et al. Among authors: clayton pt. 2017 May 25. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2017 May 25. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 28541650 Free Books & Documents. Review.
Hypermanganesemia with Dystonia 1.
Tuschl K, Clayton PT, Gospe SM Jr, Mills PB. Tuschl K, et al. Among authors: clayton pt. 2012 Aug 30 [updated 2021 Dec 23]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2012 Aug 30 [updated 2021 Dec 23]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 22934317 Free Books & Documents. Review.
Manganese and the brain.
Tuschl K, Mills PB, Clayton PT. Tuschl K, et al. Among authors: clayton pt. Int Rev Neurobiol. 2013;110:277-312. doi: 10.1016/B978-0-12-410502-7.00013-2. Int Rev Neurobiol. 2013. PMID: 24209443 Review.
Inborn errors of metabolism causing epilepsy.
Rahman S, Footitt EJ, Varadkar S, Clayton PT. Rahman S, et al. Among authors: clayton pt. Dev Med Child Neurol. 2013 Jan;55(1):23-36. doi: 10.1111/j.1469-8749.2012.04406.x. Epub 2012 Sep 24. Dev Med Child Neurol. 2013. PMID: 22998469 Free article. Review.
Disorders of cholesterol biosynthesis.
Clayton PT. Clayton PT. Arch Dis Child. 1998 Feb;78(2):185-9. doi: 10.1136/adc.78.2.185. Arch Dis Child. 1998. PMID: 9579167 Free PMC article. Review. No abstract available.
Disorders of bile acid synthesis.
Clayton PT. Clayton PT. J Inherit Metab Dis. 2011 Jun;34(3):593-604. doi: 10.1007/s10545-010-9259-3. Epub 2011 Jan 13. J Inherit Metab Dis. 2011. PMID: 21229319 Review.
Neurotransmitter diseases and related conditions.
Campeau PM, Bernard G, Clayton PT. Campeau PM, et al. Among authors: clayton pt. Mol Genet Metab. 2007 Nov;92(3):189-97. doi: 10.1016/j.ymgme.2007.08.117. Mol Genet Metab. 2007. PMID: 18038456 Review. No abstract available.
185 results