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

Year Number of Results
2001 1
2002 1
2006 2
2007 3
2008 4
2009 4
2010 3
2011 4
2012 6
2013 4
2014 3
2015 4
2016 3
2017 4
2018 2
2019 5
2020 3
2021 5
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2023 1
2024 1

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PubMed (GeneRIF) for id: 3094

55 results

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Page 1
HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling.
Malcorps M, Amor-Barris S, Burnyte B, Vilimiene R, Armirola-Ricaurte C, Grigalioniene K, Ekshteyn A, Morkuniene A, Vaitkevicius A, De Vriendt E, Baets J, Scherer SS, Ambrozaityte L, Utkus A, Jordanova A, Peeters K. Malcorps M, et al. Orphanet J Rare Dis. 2022 Oct 14;17(1):374. doi: 10.1186/s13023-022-02541-0. Orphanet J Rare Dis. 2022. PMID: 36242072 Free PMC article.
HINT1-related neuropathy in Greek patients with Charcot-Marie-Tooth disease.
Kontogeorgiou Z, Voudommatis C, Kartanou C, Pandis D, Breza M, Zambelis T, Stefanis L, Panas M, Koutsis G, Karadima G. Kontogeorgiou Z, et al. J Peripher Nerv Syst. 2021 Dec;26(4):444-448. doi: 10.1111/jns.12473. Epub 2021 Oct 29. J Peripher Nerv Syst. 2021. PMID: 34694653
HINT1 neuropathy in Norway: clinical, genetic and functional profiling.
Amor-Barris S, Høyer H, Brauteset LV, De Vriendt E, Strand L, Jordanova A, Braathen GJ, Peeters K. Amor-Barris S, et al. Orphanet J Rare Dis. 2021 Mar 4;16(1):116. doi: 10.1186/s13023-021-01746-z. Orphanet J Rare Dis. 2021. PMID: 33663550 Free PMC article.
55 results