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.
3. Induced shift in myosin heavy chain expression in myosin myopathy by endurance training. Tajsharghi H; Sunnerhagen KS; Darin N; Kyllerman M; Oldfors A J Neurol; 2004 Feb; 251(2):179-83. PubMed ID: 14991352 [TBL] [Abstract][Full Text] [Related]
4. Embryonic myosin heavy-chain mutations cause distal arthrogryposis and developmental myosin myopathy that persists postnatally. Tajsharghi H; Kimber E; Kroksmark AK; Jerre R; Tulinius M; Oldfors A Arch Neurol; 2008 Aug; 65(8):1083-90. PubMed ID: 18695058 [TBL] [Abstract][Full Text] [Related]
5. Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations. Tajsharghi H; Hilton-Jones D; Raheem O; Saukkonen AM; Oldfors A; Udd B Brain; 2010 May; 133(Pt 5):1451-9. PubMed ID: 20418530 [TBL] [Abstract][Full Text] [Related]
6. Alport syndrome. Molecular genetic aspects. Hertz JM Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970 [TBL] [Abstract][Full Text] [Related]
8. Low sequence variation in the gene encoding the human beta-myosin heavy chain. Freeman K; Nakao K; Leinwand LA Genomics; 2001 Aug; 76(1-3):73-80. PubMed ID: 11549319 [TBL] [Abstract][Full Text] [Related]
9. Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene. Villard E; Duboscq-Bidot L; Charron P; Benaiche A; Conraads V; Sylvius N; Komajda M Eur Heart J; 2005 Apr; 26(8):794-803. PubMed ID: 15769782 [TBL] [Abstract][Full Text] [Related]
10. Dominantly inherited myosin IIa myopathy caused by aberrant splicing of MYH2. Hedberg-Oldfors C; Elíasdóttir Ó; Geijer M; Lindberg C; Oldfors A BMC Neurol; 2022 Nov; 22(1):428. PubMed ID: 36380287 [TBL] [Abstract][Full Text] [Related]
11. Myopathies associated with myosin heavy chain mutations. Oldfors A; Tajsharghi H; Darin N; Lindberg C Acta Myol; 2004 Sep; 23(2):90-6. PubMed ID: 15605950 [TBL] [Abstract][Full Text] [Related]
12. Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene. Martinsson T; Oldfors A; Darin N; Berg K; Tajsharghi H; Kyllerman M; Wahlstrom J Proc Natl Acad Sci U S A; 2000 Dec; 97(26):14614-9. PubMed ID: 11114175 [TBL] [Abstract][Full Text] [Related]
13. Filamentous tangles with nemaline rods in MYH2 myopathy: a novel phenotype. Madigan NN; Polzin MJ; Cui G; Liewluck T; Alsharabati MH; Klein CJ; Windebank AJ; Mer G; Milone M Acta Neuropathol Commun; 2021 Apr; 9(1):79. PubMed ID: 33926564 [TBL] [Abstract][Full Text] [Related]
15. Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred. Dye DE; Azzarelli B; Goebel HH; Laing NG Neuromuscul Disord; 2006 Jun; 16(6):357-60. PubMed ID: 16684601 [TBL] [Abstract][Full Text] [Related]
16. A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies. D'Amico A; Fattori F; Bellacchio E; Catteruccia M; Servidei S; Bertini E Neuromuscul Disord; 2013 May; 23(5):437-40. PubMed ID: 23489661 [TBL] [Abstract][Full Text] [Related]