Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1976 1
1977 2
1979 1
1980 1
1981 1
1982 4
1983 2
1984 4
1985 2
1986 1
1987 5
1989 3
1990 5
1991 2
1992 5
1993 3
1994 3
1996 2
1997 1
1998 4
1999 5
2000 2
2001 4
2002 1
2003 2
2004 4
2005 2
2006 3
2007 2
2008 4
2009 2
2010 6
2011 5
2012 3
2013 4
2014 4
2015 4
2016 5
2017 5
2018 4
2019 5
2020 2
2021 2
2022 0
Text availability
Article attribute
Article type
Publication date

Search Results

122 results
Results by year
Filters applied: . Clear all
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.
Type 1 Tyrosinaemia.
Mannion MA, Smith A, Mayne P, Monavari AA. Mannion MA, et al. Among authors: mayne p. Ir Med J. 2016 Jun 10;109(6):426. Ir Med J. 2016. PMID: 27814443
Newborn screening for homocystinurias: Recent recommendations versus current practice.
Keller R, Chrastina P, Pavlíková M, Gouveia S, Ribes A, Kölker S, Blom HJ, Baumgartner MR, Bártl J, Dionisi-Vici C, Gleich F, Morris AA, Kožich V, Huemer M; individual contributors of the European Network and Registry for Homocystinurias and Methylation Defects (E-HOD), Barić I, Ben-Omran T, Blasco-Alonso J, Bueno Delgado MA, Carducci C, Cassanello M, Cerone R, Couce ML, Crushell E, Delgado Pecellin C, Dulin E, Espada M, Ferino G, Fingerhut R, Garcia Jimenez I, Gonzalez Gallego I, González-Irazabal Y, Gramer G, Juan Fita MJ, Karg E, Klein J, Konstantopoulou V, la Marca G, Leão Teles E, Leuzzi V, Lilliu F, Lopez RM, Lund AM, Mayne P, Meavilla S, Moat SJ, Okun JG, Pasquini E, Pedron-Giner CC, Racz GZ, Ruiz Gomez MA, Vilarinho L, Yahyaoui R, Zerjav Tansek M, Zetterström RH, Zeyda M. Keller R, et al. Among authors: mayne p. J Inherit Metab Dis. 2019 Jan;42(1):128-139. doi: 10.1002/jimd.12034. J Inherit Metab Dis. 2019. PMID: 30740731
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
Maple syrup urine disease: Clinical outcomes, metabolic control, and genotypes in a screened population after four decades of newborn bloodspot screening in the Republic of Ireland.
O'Reilly D, Crushell E, Hughes J, Ryan S, Rogers Y, Borovickova I, Mayne P, Riordan M, Awan A, Carson K, Hunter K, Lynch B, Shahwan A, Rüfenacht V, Häberle J, Treacy EP, Monavari AA, Knerr I. O'Reilly D, et al. Among authors: mayne p. J Inherit Metab Dis. 2021 May;44(3):639-655. doi: 10.1002/jimd.12337. Epub 2020 Dec 20. J Inherit Metab Dis. 2021. PMID: 33300147
122 results