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

Year Number of Results
1993 1
1998 1
2003 1
2006 1
2007 3
2008 3
2009 2
2010 1
2011 1
2012 3
2013 2
2014 3
2015 3
2016 1
2017 2
2018 5
2019 1
2021 3
2022 4
2023 3
2024 2

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36 results

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Page 1
Gap junctions couple astrocytes and oligodendrocytes.
Orthmann-Murphy JL, Abrams CK, Scherer SS. Orthmann-Murphy JL, et al. Among authors: abrams ck. J Mol Neurosci. 2008 May;35(1):101-16. doi: 10.1007/s12031-007-9027-5. J Mol Neurosci. 2008. PMID: 18236012 Free PMC article. Review.
AAV1.NT-3 gene therapy for X-linked Charcot-Marie-Tooth neuropathy type 1.
Ozes B, Myers M, Moss K, Mckinney J, Ridgley A, Chen L, Bai S, Abrams CK, Freidin MM, Mendell JR, Sahenk Z. Ozes B, et al. Among authors: abrams ck. Gene Ther. 2022 Apr;29(3-4):127-137. doi: 10.1038/s41434-021-00231-3. Epub 2021 Feb 4. Gene Ther. 2022. PMID: 33542455 Free PMC article.
GJB1 Disorders: Charcot-Marie-Tooth Neuropathy (CMT1X) and Central Nervous System Phenotypes.
Abrams CK. Abrams CK. 1998 Jun 18 [updated 2024 Apr 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 1998 Jun 18 [updated 2024 Apr 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301548 Free Books & Documents. Review.
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders.
Borgia P, Baldassari S, Pedemonte N, Alkhunaizi E, D'Onofrio G, Tortora D, Calì E, Scudieri P, Balagura G, Musante I, Diana MC, Pedemonte M, Vari MS, Iacomino M, Riva A, Chimenz R, Mangano GD, Mohammadi MH, Toosi MB, Ashrafzadeh F, Imannezhad S, Karimiani EG, Accogli A, Schiaffino MC, Maghnie M, Soler MA, Echiverri K, Abrams CK, Striano P, Fortuna S, Maroofian R, Houlden H, Zara F, Fiorillo C, Salpietro V. Borgia P, et al. Among authors: abrams ck. Orphanet J Rare Dis. 2022 Jul 19;17(1):286. doi: 10.1186/s13023-022-02415-5. Orphanet J Rare Dis. 2022. PMID: 35854306 Free PMC article.
36 results