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Results by year

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

Year Number of Results
1979 1
1982 1
1983 1
1984 3
1985 2
1986 1
1987 5
1989 3
1990 5
1991 1
1992 3
1993 2
1996 1
1997 1
1998 1
1999 3
2001 2
2002 1
2003 2
2004 4
2006 1
2008 4
2009 1
2010 3
2011 1
2012 2
2013 1
2014 1
2015 2
2016 2
2017 1
2018 2
2019 1
2024 0

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61 results

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Page 1
Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.
Morris AA, Kožich V, Santra S, Andria G, Ben-Omran TI, Chakrapani AB, Crushell E, Henderson MJ, Hochuli M, Huemer M, Janssen MC, Maillot F, Mayne PD, McNulty J, Morrison TM, Ogier H, O'Sullivan S, Pavlíková M, de Almeida IT, Terry A, Yap S, Blom HJ, Chapman KA. Morris AA, et al. Among authors: mayne pd. J Inherit Metab Dis. 2017 Jan;40(1):49-74. doi: 10.1007/s10545-016-9979-0. Epub 2016 Oct 24. J Inherit Metab Dis. 2017. PMID: 27778219 Free PMC article. Review.
Pseudohyperkalaemia.
Axford JS, Rampton DS, Mayne PD. Axford JS, et al. Among authors: mayne pd. Br Med J (Clin Res Ed). 1985 Oct 26;291(6503):1202-3. doi: 10.1136/bmj.291.6503.1202-b. Br Med J (Clin Res Ed). 1985. PMID: 3931852 Free PMC article. No abstract available.
Amino acids: analytical aspects.
Mayne PD, Roche G, Deverell D. Mayne PD, et al. J Inherit Metab Dis. 2001 Apr;24(2):305-8. doi: 10.1023/a:1010343707174. J Inherit Metab Dis. 2001. PMID: 11405350
Incidence of Congenital Hypothyroidism Over 37 Years in Ireland.
McGrath N, Hawkes CP, McDonnell CM, Cody D, O'Connell SM, Mayne PD, Murphy NP. McGrath N, et al. Among authors: mayne pd. Pediatrics. 2018 Oct;142(4):e20181199. doi: 10.1542/peds.2018-1199. Pediatrics. 2018. PMID: 30242075
Myxoedema coma.
Cullen MJ, Mayne PD, Sliney I. Cullen MJ, et al. Among authors: mayne pd. Ir J Med Sci. 1979 Dec;148(1):201. doi: 10.1007/BF02938083. Ir J Med Sci. 1979. PMID: 27517421
3-Methylglutaconic aciduria in pregnancy.
Walsh R, Conway H, Roche G, Naughten E, Mayne PD. Walsh R, et al. Among authors: mayne pd. Lancet. 1997 Mar 15;349(9054):776. doi: 10.1016/s0140-6736(05)60201-2. Lancet. 1997. PMID: 9074583 No abstract available.
Clinical, biochemical, and genetic features of four patients with short-chain enoyl-CoA hydratase (ECHS1) deficiency.
Fitzsimons PE, Alston CL, Bonnen PE, Hughes J, Crushell E, Geraghty MT, Tetreault M, O'Reilly P, Twomey E, Sheikh Y, Walsh R, Waterham HR, Ferdinandusse S, Wanders RJA, Taylor RW, Pitt JJ, Mayne PD. Fitzsimons PE, et al. Among authors: mayne pd. Am J Med Genet A. 2018 May;176(5):1115-1127. doi: 10.1002/ajmg.a.38658. Epub 2018 Mar 25. Am J Med Genet A. 2018. PMID: 29575569 Free PMC article.
61 results