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Results by year

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

Year Number of Results
1970 1
1986 1
1987 3
1988 2
1989 3
1990 8
1991 6
1992 1
1993 8
1994 5
1995 4
1996 7
1997 1
1998 7
1999 2
2000 3
2001 1
2002 6
2003 5
2004 5
2005 5
2006 6
2007 9
2008 11
2009 7
2010 5
2011 5
2012 6
2013 8
2014 8
2015 7
2016 5
2017 9
2018 8
2019 5
2020 14
2021 13
2022 7
2023 6
2024 0

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Publication date

PubMed for id: 2548

204 results

Results by year

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Page 1
Phase I study of liver depot gene therapy in late-onset Pompe disease.
Smith EC, Hopkins S, Case LE, Xu M, Walters C, Dearmey S, Han SO, Spears TG, Chichester JA, Bossen EH, Hornik CP, Cohen JL, Bali D, Kishnani PS, Koeberl DD. Smith EC, et al. Mol Ther. 2023 Jul 5;31(7):1994-2004. doi: 10.1016/j.ymthe.2023.02.014. Epub 2023 Feb 18. Mol Ther. 2023. PMID: 36805083 Clinical Trial.
Classic infantile-onset Pompe disease with histopathological neurologic findings linked to a novel GAA gene 4 bp deletion: A case study.
Cerón-Rodríguez M, Castillo-García D, Acosta-Rodríguez-Bueno CP, Aguirre-Hernández J, Murillo-Eliosa JR, Valencia-Mayoral P, Escobar-Sánchez A, Salgado-Loza JL. Cerón-Rodríguez M, et al. Mol Genet Genomic Med. 2022 Jul;10(7):e1957. doi: 10.1002/mgg3.1957. Epub 2022 May 9. Mol Genet Genomic Med. 2022. PMID: 35532199 Free PMC article.
Late Onset Pompe Disease with Novel Mutations and Atypical Phenotypes.
Chawla T, Preethish-Kumar V, Polavarapu K, Vengalil S, Bardhan M, Puri R, Verma J, Christopher R, Supriya M, Nashi S, Prasad C, Nadeesh B, Nalini A. Chawla T, et al. J Neuromuscul Dis. 2022;9(2):261-273. doi: 10.3233/JND-210728. J Neuromuscul Dis. 2022. PMID: 34864681
Broad variation in phenotypes for common GAA genotypes in Pompe disease.
Niño MY, In't Groen SLM, de Faria DOS, Hoogeveen-Westerveld M, van den Hout HJMP, van der Ploeg AT, Bergsma AJ, Pijnappel WWMP. Niño MY, et al. Hum Mutat. 2021 Nov;42(11):1461-1472. doi: 10.1002/humu.24272. Epub 2021 Sep 8. Hum Mutat. 2021. PMID: 34405923 Free PMC article.
204 results