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Results by year

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

Year Number of Results
1997 4
1998 2
1999 1
2001 3
2002 2
2003 1
2004 2
2006 1
2007 1
2008 4
2009 1
2010 1
2011 2
2012 3
2013 3
2014 3
2015 3
2016 3
2017 3
2018 5
2019 4
2020 5
2021 8
2022 3
2024 0

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PubMed for id: 934627

61 results

Results by year

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Page 1
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.
Alonso-Pérez J, González-Quereda L, Bruno C, Panicucci C, Alavi A, Nafissi S, Nilipour Y, Zanoteli E, Isihi LMA, Melegh B, Hadzsiev K, Muelas N, Vílchez JJ, Dourado ME, Kadem N, Kutluk G, Umair M, Younus M, Pegorano E, Bello L, Crawford TO, Suárez-Calvet X, Töpf A, Guglieri M, Marini-Bettolo C, Gallano P, Straub V, Díaz-Manera J. Alonso-Pérez J, et al. Brain. 2022 Apr 18;145(2):596-606. doi: 10.1093/brain/awab301. Brain. 2022. PMID: 34515763 Free PMC article.
Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.
Tan D, Ge L, Fan Y, Chang X, Wang S, Wei C, Ding J, Liu A, Wang S, Li X, Gao K, Yang H, Que C, Huang Z, Li C, Zhu Y, Mao B, Jin B, Hua Y, Zhang X, Zhang B, Zhu W, Zhang C, Wang Y, Yuan Y, Jiang Y, Rutkowski A, Bönnemann CG, Wu X, Xiong H. Tan D, et al. Orphanet J Rare Dis. 2021 Jul 19;16(1):319. doi: 10.1186/s13023-021-01950-x. Orphanet J Rare Dis. 2021. PMID: 34281576 Free PMC article.
Diseases related to Notch glycosylation.
Matsumoto K, Luther KB, Haltiwanger RS. Matsumoto K, et al. Mol Aspects Med. 2021 Jun;79:100938. doi: 10.1016/j.mam.2020.100938. Epub 2020 Dec 16. Mol Aspects Med. 2021. PMID: 33341260 Review.
61 results