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Results by year

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

Year Number of Results
1979 4
1981 1
1982 1
1984 1
1985 1
1986 2
1991 3
1992 1
1993 1
1995 1
1996 2
1997 3
1998 2
1999 4
2000 5
2001 5
2002 2
2003 3
2004 1
2005 4
2006 7
2007 6
2008 2
2009 5
2010 4
2011 4
2012 5
2013 11
2014 15
2015 8
2016 6
2017 6
2018 15
2019 17
2020 15
2021 13
2022 14
2023 17
2024 8

Text availability

Article attribute

Article type

Publication date

PubMed for id: 370750

191 results

Results by year

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Page 1
Motor protein mutations cause a new form of hereditary spastic paraplegia.
Caballero Oteyza A, Battaloğlu E, Ocek L, Lindig T, Reichbauer J, Rebelo AP, Gonzalez MA, Zorlu Y, Ozes B, Timmann D, Bender B, Woehlke G, Züchner S, Schöls L, Schüle R. Caballero Oteyza A, et al. Neurology. 2014 Jun 3;82(22):2007-16. doi: 10.1212/WNL.0000000000000479. Epub 2014 May 7. Neurology. 2014. PMID: 24808017 Free PMC article.
Progressive ataxia of Charolais cattle highlights a role of KIF1C in sustainable myelination.
Duchesne A, Vaiman A, Frah M, Floriot S, Legoueix-Rodriguez S, Desmazières A, Fritz S, Beauvallet C, Albaric O, Venot E, Bertaud M, Saintilan R, Guatteo R, Esquerré D, Branchu J, Fleming A, Brice A, Darios F, Vilotte JL, Stevanin G, Boichard D, El Hachimi KH. Duchesne A, et al. PLoS Genet. 2018 Aug 1;14(8):e1007550. doi: 10.1371/journal.pgen.1007550. eCollection 2018 Aug. PLoS Genet. 2018. PMID: 30067756 Free PMC article.
Expanding the allelic spectrum of ELOVL4-related autosomal recessive neuro-ichthyosis.
Alabdulrazzaq F, Alanzi T, Al-Balool HH, Gardham A, Wakeling E, Leitch HG, AlSayed M, Abdulrahim M, Aladwani A, Romito A, Kampe K, Ferdinandusse S, Aboelanine AH, Abdullah A, Alwadani A, Bastaki L, Vaz FM, Bertoli-Avella AM, Marafi D. Alabdulrazzaq F, et al. Mol Genet Genomic Med. 2023 Dec;11(12):e2256. doi: 10.1002/mgg3.2256. Epub 2023 Aug 18. Mol Genet Genomic Med. 2023. PMID: 37592902 Free PMC article.
191 results