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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2004 | 1 |
2010 | 1 |
2011 | 1 |
2013 | 1 |
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2024 | 0 |
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Late form of Pompe disease with glycogen storage in peripheral nerves axons.
J Neurol Sci. 2011 Feb 15;301(1-2):59-62. doi: 10.1016/j.jns.2010.10.031. Epub 2010 Nov 25.
J Neurol Sci. 2011.
PMID: 21109266
Twenty-two novel mutations in the lysosomal alpha-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II.
Hermans MM, van Leenen D, Kroos MA, Beesley CE, Van Der Ploeg AT, Sakuraba H, Wevers R, Kleijer W, Michelakakis H, Kirk EP, Fletcher J, Bosshard N, Basel-Vanagaite L, Besley G, Reuser AJ.
Hermans MM, et al.
Hum Mutat. 2004 Jan;23(1):47-56. doi: 10.1002/humu.10286.
Hum Mutat. 2004.
PMID: 14695532
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Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literature.
Remiche G, Ronchi D, Magri F, Lamperti C, Bordoni A, Moggio M, Bresolin N, Comi GP.
Remiche G, et al.
J Neurol. 2014 Jan;261(1):83-97. doi: 10.1007/s00415-013-7137-2. Epub 2013 Oct 25.
J Neurol. 2014.
PMID: 24158270
Review.
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