These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
182 related articles for article (PubMed ID: 21361913)
1. 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 Clin Genet; 2012 Apr; 81(4):394-8. PubMed ID: 21361913 [TBL] [Abstract][Full Text] [Related]
2. BAG3 mutation in a patient with atypical phenotypes of myofibrillar myopathy and Charcot-Marie-Tooth disease. Kim SJ; Nam SH; Kanwal S; Nam DE; Yoo DH; Chae JH; Suh YL; Chung KW; Choi BO Genes Genomics; 2018 Dec; 40(12):1269-1277. PubMed ID: 30145633 [TBL] [Abstract][Full Text] [Related]
3. 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 Acta Myol; 2021 Dec; 40(4):177-183. PubMed ID: 35047758 [TBL] [Abstract][Full Text] [Related]
4. BAG3-related myopathy, polyneuropathy and cardiomyopathy with long QT syndrome. Kostera-Pruszczyk A; Suszek M; Płoski R; Franaszczyk M; Potulska-Chromik A; Pruszczyk P; Sadurska E; Karolczak J; Kamińska AM; Rędowicz MJ J Muscle Res Cell Motil; 2015 Dec; 36(6):423-32. PubMed ID: 26545904 [TBL] [Abstract][Full Text] [Related]
5. BAG3 myopathy is not always associated with cardiomyopathy. Andersen AG; Fornander F; Schrøder HD; Krag T; Straub V; Duno M; Vissing J Neuromuscul Disord; 2018 Sep; 28(9):798-801. PubMed ID: 30061062 [TBL] [Abstract][Full Text] [Related]
6. Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation. Odgerel Z; Sarkozy A; Lee HS; McKenna C; Rankin J; Straub V; Lochmüller H; Paola F; D'Amico A; Bertini E; Bushby K; Goldfarb LG Neuromuscul Disord; 2010 Jul; 20(7):438-42. PubMed ID: 20605452 [TBL] [Abstract][Full Text] [Related]
7. BAG3 Myopathy Presenting With Prominent Neuropathic Phenotype and No Cardiac or Respiratory Involvement: A Case Report and Literature Review. Malatesta L; Arya K; Gokden M; Stefans V; Veerapandiyan A J Clin Neuromuscul Dis; 2020 Jun; 21(4):230-239. PubMed ID: 32453099 [TBL] [Abstract][Full Text] [Related]
8. 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 J Clin Neuromuscul Dis; 2022 Sep; 24(1):49-54. PubMed ID: 36005473 [TBL] [Abstract][Full Text] [Related]
9. Dysregulated autophagy in restrictive cardiomyopathy due to Pro209Leu mutation in BAG3. Schänzer A; Rupp S; Gräf S; Zengeler D; Jux C; Akintürk H; Gulatz L; Mazhari N; Acker T; Van Coster R; Garvalov BK; Hahn A Mol Genet Metab; 2018 Mar; 123(3):388-399. PubMed ID: 29338979 [TBL] [Abstract][Full Text] [Related]
10. Xu Y; Liu SX; Xu WB; Luo JM; Niu JW; Liu Z; Gao JM; Wang JL; Dai Y; Wang MZ Chin Med Sci J; 2021 Dec; 36(4):265-278. PubMed ID: 34986963 [TBL] [Abstract][Full Text] [Related]
17. Genetic compensation prevents myopathy and heart failure in an in vivo model of Bag3 deficiency. Diofano F; Weinmann K; Schneider I; Thiessen KD; Rottbauer W; Just S PLoS Genet; 2020 Nov; 16(11):e1009088. PubMed ID: 33137814 [TBL] [Abstract][Full Text] [Related]