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Results by year

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

Year Number of Results
1965 1
1974 1
1975 6
1976 7
1977 11
1978 5
1979 13
1980 18
1981 17
1982 17
1983 17
1984 25
1985 31
1986 25
1987 32
1988 18
1989 43
1990 27
1991 31
1992 31
1993 47
1994 51
1995 50
1996 59
1997 48
1998 58
1999 61
2000 68
2001 57
2002 37
2003 55
2004 46
2005 62
2006 53
2007 77
2008 62
2009 65
2010 64
2011 85
2012 98
2013 104
2014 104
2015 114
2016 88
2017 100
2018 104
2019 155
2020 136
2021 166
2022 178
2023 173
2024 54

Text availability

Article attribute

Article type

Publication date

PubMed for id: 1708324

2,806 results

Results by year

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Page 1
Newborn screening for X-linked adrenoleukodystrophy in New York State: diagnostic protocol, surveillance protocol and treatment guidelines.
Vogel BH, Bradley SE, Adams DJ, D'Aco K, Erbe RW, Fong C, Iglesias A, Kronn D, Levy P, Morrissey M, Orsini J, Parton P, Pellegrino J, Saavedra-Matiz CA, Shur N, Wasserstein M, Raymond GV, Caggana M. Vogel BH, et al. Mol Genet Metab. 2015 Apr;114(4):599-603. doi: 10.1016/j.ymgme.2015.02.002. Epub 2015 Feb 12. Mol Genet Metab. 2015. PMID: 25724074
Corrigendum: Newborn screening for X-linked adrenoleukodystrophy in Italy: diagnostic algorithm and disease monitoring.
Bonaventura E, Alberti L, Lucchi S, Cappelletti L, Fazzone S, Cattaneo E, Bellini M, Izzo G, Parazzini C, Bosetti A, Di Profio E, Fiore G, Ferrario M, Mameli C, Sangiorgio A, Masnada S, Zuccotti GV, Veggiotti P, Spaccini L, Iascone M, Verduci E, Cereda C, Tonduti D; XALD-NBS Study Group. Bonaventura E, et al. Front Neurol. 2024 Mar 6;15:1376447. doi: 10.3389/fneur.2024.1376447. eCollection 2024. Front Neurol. 2024. PMID: 38510379 Free PMC article.
Patient-reported impact of symptoms in adrenoleukodystrophy (PRISM-ALD).
Varma A, Weinstein J, Seabury J, Rosero S, Dilek N, Heatwole J, Engebrecht C, Khosa S, Chung K, Paker A, Woo A, Brooks G, Beals C, Gandhi R, Heatwole C. Varma A, et al. Orphanet J Rare Dis. 2024 Mar 19;19(1):127. doi: 10.1186/s13023-024-03129-6. Orphanet J Rare Dis. 2024. PMID: 38504253 Free PMC article.
2,806 results