Tajsharghi H - Search Results

1

Mutations and sequence variation in the human myosin heavy chain IIa gene (MYH2).

Tajsharghi H, Darin N, Rekabdar E, Kyllerman M, Wahlström J, Martinsson T, Oldfors A. Tajsharghi H, et al. Eur J Hum Genet. 2005 May;13(5):617-22. doi: 10.1038/sj.ejhg.5201375. Eur J Hum Genet. 2005. PMID: 15741996

2

Induced shift in myosin heavy chain expression in myosin myopathy by endurance training.

Tajsharghi H, Sunnerhagen KS, Darin N, Kyllerman M, Oldfors A. Tajsharghi H, et al. J Neurol. 2004 Feb;251(2):179-83. doi: 10.1007/s00415-004-0295-5. J Neurol. 2004. PMID: 14991352

3

A Caenorhabditis elegans model of the myosin heavy chain IIa E706K [corrected] mutation.

Tajsharghi H, Pilon M, Oldfors A. Tajsharghi H, et al. Ann Neurol. 2005 Sep;58(3):442-8. doi: 10.1002/ana.20594. Ann Neurol. 2005. PMID: 16130113

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. Tajsharghi H, et al. Arch Neurol. 2008 Aug;65(8):1083-90. doi: 10.1001/archneur.65.8.1083. Arch Neurol. 2008. PMID: 18695058

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. Tajsharghi H, et al. Brain. 2010 May;133(Pt 5):1451-9. doi: 10.1093/brain/awq083. Brain. 2010. PMID: 20418530

6

Myosinopathies: pathology and mechanisms.

Tajsharghi H, Oldfors A. Tajsharghi H, et al. Acta Neuropathol. 2013 Jan;125(1):3-18. doi: 10.1007/s00401-012-1024-2. Epub 2012 Aug 5. Acta Neuropathol. 2013. PMID: 22918376 Free PMC article. Review.

7

Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations.

Tajsharghi H, Hammans S, Lindberg C, Lossos A, Clarke NF, Mazanti I, Waddell LB, Fellig Y, Foulds N, Katifi H, Webster R, Raheem O, Udd B, Argov Z, Oldfors A. Tajsharghi H, et al. Eur J Hum Genet. 2014 Jun;22(6):801-8. doi: 10.1038/ejhg.2013.250. Epub 2013 Nov 6. Eur J Hum Genet. 2014. PMID: 24193343 Free PMC article.

8

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. Martinsson T, et al. Among authors: tajsharghi h. Proc Natl Acad Sci U S A. 2000 Dec 19;97(26):14614-9. doi: 10.1073/pnas.250289597. Proc Natl Acad Sci U S A. 2000. PMID: 11114175 Free PMC article.

9

Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age.

Tajsharghi H, Thornell LE, Darin N, Martinsson T, Kyllerman M, Wahlström J, Oldfors A. Tajsharghi H, et al. Neurology. 2002 Mar 12;58(5):780-6. doi: 10.1212/wnl.58.5.780. Neurology. 2002. PMID: 11889243

10

Myopathies associated with myosin heavy chain mutations.

Oldfors A, Tajsharghi H, Darin N, Lindberg C. Oldfors A, et al. Among authors: tajsharghi h. Acta Myol. 2004 Sep;23(2):90-6. Acta Myol. 2004. PMID: 15605950 Review.

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