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Results by year

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

Year Number of Results
1984 1
1993 4
1994 4
1996 1
1997 1
1998 2
1999 3
2000 3
2001 2
2002 1
2003 2
2004 2
2005 3
2006 1
2007 3
2008 3
2009 6
2010 10
2011 7
2012 5
2013 4
2014 8
2015 11
2016 9
2017 14
2018 23
2019 19
2020 15
2021 15
2022 26
2023 10
2024 0

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PubMed for id: 4141

194 results

Results by year

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Page 1
Deep phenotyping of MARS1 (interstitial lung and liver disease) and LARS1 (infantile liver failure syndrome 1) recessive multisystemic disease using Human Phenotype Ontology annotation: Overlap and differences. Case report and review of literature.
La Fay C, Hoebeke C, Juzaud M, Spraul A, Heux P, Dubus JC, Hadchouel A, Fabre A. La Fay C, et al. Eur J Med Genet. 2021 Nov;64(11):104334. doi: 10.1016/j.ejmg.2021.104334. Epub 2021 Sep 5. Eur J Med Genet. 2021. PMID: 34496286 Review.
Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2.
Gonzalez M, McLaughlin H, Houlden H, Guo M, Yo-Tsen L, Hadjivassilious M, Speziani F, Yang XL, Antonellis A, Reilly MM, Züchner S; Inherited Neuropathy Consortium. Gonzalez M, et al. J Neurol Neurosurg Psychiatry. 2013 Nov;84(11):1247-9. doi: 10.1136/jnnp-2013-305049. Epub 2013 Jun 1. J Neurol Neurosurg Psychiatry. 2013. PMID: 23729695 Free PMC article.
Methionyl-tRNA synthetase.
Deniziak MA, Barciszewski J. Deniziak MA, et al. Acta Biochim Pol. 2001;48(2):337-50. Acta Biochim Pol. 2001. PMID: 11732605 Free article. Review.
194 results