Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
My NCBI Filters
Results by year

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

Year Number of Results
1993 3
1994 1
1995 1
1996 1
1998 1
1999 5
2001 1
2002 2
2003 3
2004 5
2005 5
2006 3
2007 3
2008 12
2009 8
2010 7
2011 15
2012 17
2013 10
2014 9
2015 7
2016 7
2017 6
2018 6
2019 7
2020 6
2021 2
Text availability
Article attribute
Article type
Publication date

PubMed Links for id: 2273

130 results
Results by year
Filters applied: . Clear all
Page 1
Exome Sequencing Identified a Splice Site Mutation in FHL1 that Causes Uruguay Syndrome, an X-Linked Disorder With Skeletal Muscle Hypertrophy and Premature Cardiac Death.
Xue Y, Schoser B, Rao AR, Quadrelli R, Vaglio A, Rupp V, Beichler C, Nelson SF, Schapacher-Tilp G, Windpassinger C, Wilcox WR. Xue Y, et al. Circ Cardiovasc Genet. 2016 Apr;9(2):130-5. doi: 10.1161/CIRCGENETICS.115.001193. Epub 2016 Mar 1. Circ Cardiovasc Genet. 2016. PMID: 26933038 Free PMC article.
Development of autoantibodies against muscle-specific FHL1 in severe inflammatory myopathies.
Albrecht I, Wick C, Hallgren Å, Tjärnlund A, Nagaraju K, Andrade F, Thompson K, Coley W, Phadke A, Diaz-Gallo LM, Bottai M, Nennesmo I, Chemin K, Herrath J, Johansson K, Wikberg A, Ytterberg AJ, Zubarev RA, Danielsson O, Krystufkova O, Vencovsky J, Landegren N, Wahren-Herlenius M, Padyukov L, Kämpe O, Lundberg IE. Albrecht I, et al. J Clin Invest. 2015 Dec;125(12):4612-24. doi: 10.1172/JCI81031. Epub 2015 Nov 9. J Clin Invest. 2015. PMID: 26551678 Free PMC article.
130 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page