PubMed for id: 414119

Year	Number of Results
1982	1
1983	1
1985	1
1987	1
1988	1
1993	1
1996	1
1998	2
2001	3
2002	1
2003	2
2004	3
2005	2
2006	3
2007	3
2008	1
2009	5
2010	7
2011	8
2012	5
2013	12
2014	7
2015	9
2016	14
2017	10
2018	10
2019	3
2020	13
2021	6
2022	6
2023	3
2024	1

1

BAG3-related myofibrillar myopathy: a further observation with cardiomyopathy at onset in pediatric age.

Scarpini G, Valentino ML, Giannotta M, Ragni L, Torella A, Columbaro M, Nigro V, Pini A. Scarpini G, et al. Acta Myol. 2021 Dec 31;40(4):177-183. doi: 10.36185/2532-1900-061. eCollection 2021 Dec. Acta Myol. 2021. PMID: 35047758 Free PMC article.

2

BAG3-Related Myofibrillar Myopathy Presenting as Hypercapnia: A Case Report and Literature Review.

Xu Y, Liu SX, Xu WB, Luo JM, Niu JW, Liu Z, Gao JM, Wang JL, Dai Y, Wang MZ. Xu Y, et al. Chin Med Sci J. 2021 Dec 31;36(4):265-278. doi: 10.24920/003883. Chin Med Sci J. 2021. PMID: 34986963 Review.

3

Proteome and transcriptome profiling of equine myofibrillar myopathy identifies diminished peroxiredoxin 6 and altered cysteine metabolic pathways.

Valberg SJ, Perumbakkam S, McKenzie EC, Finno CJ. Valberg SJ, et al. Physiol Genomics. 2018 Dec 1;50(12):1036-1050. doi: 10.1152/physiolgenomics.00044.2018. Epub 2018 Oct 5. Physiol Genomics. 2018. PMID: 30289745 Free PMC article.

4

BAG3-related myofibrillar myopathy in a Chinese family.

Lee HC, Cherk SW, Chan SK, Wong S, Tong TW, Ho WS, Chan AY, Lee KC, Mak CM. Lee HC, et al. Clin Genet. 2012 Apr;81(4):394-8. doi: 10.1111/j.1399-0004.2011.01659.x. Epub 2011 Apr 4. Clin Genet. 2012. PMID: 21361913

5

Differential effects of pharmacological modulators of cardiac myofibrillar ATPase activity in normal and myopathic (BIO 14.6) hamsters.

Silver PJ, Monteforte PB. Silver PJ, et al. Eur J Pharmacol. 1988 Mar 15;147(3):335-42. doi: 10.1016/0014-2999(88)90166-5. Eur J Pharmacol. 1988. PMID: 2967769

6

Distal hereditary motor neuronopathy as a new phenotype associated with variants in BAG3.

de Fuenmayor-Fernández de la Hoz CP, Lupo V, Bermejo-Guerrero L, Martín-Jiménez P, Hernández-Laín A, Olivé M, Gallardo E, Esteban-Pérez J, Espinós C, Domínguez-González C. de Fuenmayor-Fernández de la Hoz CP, et al. J Neurol. 2024 Feb;271(2):986-994. doi: 10.1007/s00415-023-12039-9. Epub 2023 Oct 31. J Neurol. 2024. PMID: 37907725

7

A novel in-frame deletion in MYOT causes an early adult onset distal myopathy.

Guglielmi V, Pancheri E, Cannone E, Nigro V, Malatesta M, Vettori A, Giorgetti A, Torella A, Aurino S, Cisterna B, Marchetto G, Tomelleri G, Tonin P, Schiavone M, Vattemi G. Guglielmi V, et al. Clin Genet. 2023 Dec;104(6):705-710. doi: 10.1111/cge.14413. Epub 2023 Aug 8. Clin Genet. 2023. PMID: 37553249

8

Myofibrillar myopathy hallmarks associated with ZAK deficiency.

Stonadge A, Genzor AV, Russell A, Hamed MF, Romero N, Evans G, Pownall ME, Bekker-Jensen S, Blanco G. Stonadge A, et al. Hum Mol Genet. 2023 Aug 26;32(17):2751-2770. doi: 10.1093/hmg/ddad113. Hum Mol Genet. 2023. PMID: 37427997 Free PMC article.

9

Wide Spectrum of Cardiac Phenotype in Myofibrillar Myopathy Associated With a Bcl-2-Associated Athanogene 3 Mutation: A Case Report and Literature Review.

Akaba Y, Takeguchi R, Tanaka R, Makita Y, Kimura T, Yanagi K, Kaname T, Nishino I, Takahashi S. Akaba Y, et al. J Clin Neuromuscul Dis. 2022 Sep 1;24(1):49-54. doi: 10.1097/CND.0000000000000392. J Clin Neuromuscul Dis. 2022. PMID: 36005473 Review.

10

Isoform-specific mutation in Dystonin-b gene causes late-onset protein aggregate myopathy and cardiomyopathy.

Yoshioka N, Kurose M, Yano M, Tran DM, Okuda S, Mori-Ochiai Y, Horie M, Nagai T, Nishino I, Shibata S, Takebayashi H. Yoshioka N, et al. Elife. 2022 Aug 9;11:e78419. doi: 10.7554/eLife.78419. Elife. 2022. PMID: 35942699 Free PMC article.

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