Oldfors A - Search Results

1

Defective regulation of contractile function in muscle fibres carrying an E41K beta-tropomyosin mutation.

Ochala J, Li M, Ohlsson M, Oldfors A, Larsson L. Ochala J, et al. Among authors: oldfors a. J Physiol. 2008 Jun 15;586(12):2993-3004. doi: 10.1113/jphysiol.2008.153650. Epub 2008 Apr 17. J Physiol. 2008. PMID: 18420702 Free PMC article.

2

[Heart failure in amyloidosis--a rare but treatable disease].

Ohlsson M, Oldfors A, Hallgren P. Ohlsson M, et al. Among authors: oldfors a. Lakartidningen. 2002 May 23;99(21):2386-8, 2391. Lakartidningen. 2002. PMID: 12090165 Swedish.

3

Follow-up of nemaline myopathy in two patients with novel mutations in the skeletal muscle alpha-actin gene (ACTA1).

Ohlsson M, Tajsharghi H, Darin N, Kyllerman M, Oldfors A. Ohlsson M, et al. Among authors: oldfors a. Neuromuscul Disord. 2004 Sep;14(8-9):471-5. doi: 10.1016/j.nmd.2004.05.016. Neuromuscul Disord. 2004. PMID: 15336687

4

Mitochondrial abnormalities in inclusion-body myositis.

Oldfors A, Moslemi AR, Jonasson L, Ohlsson M, Kollberg G, Lindberg C. Oldfors A, et al. Neurology. 2006 Jan 24;66(2 Suppl 1):S49-55. doi: 10.1212/01.wnl.0000192127.63013.8d. Neurology. 2006. PMID: 16432145 Review.

5

Muscle cell and motor protein function in patients with a IIa myosin missense mutation (Glu-706 to Lys).

Li M, Lionikas A, Yu F, Tajsharghi H, Oldfors A, Larsson L. Li M, et al. Among authors: oldfors a. Neuromuscul Disord. 2006 Nov;16(11):782-91. doi: 10.1016/j.nmd.2006.07.023. Epub 2006 Sep 26. Neuromuscul Disord. 2006. PMID: 17005402 Free PMC article.

6

Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutation.

Tajsharghi H, Kimber E, Holmgren D, Tulinius M, Oldfors A. Tajsharghi H, et al. Among authors: oldfors a. Neurology. 2007 Mar 6;68(10):772-5. doi: 10.1212/01.wnl.0000256339.40667.fb. Neurology. 2007. PMID: 17339586

7

Effects of a R133W beta-tropomyosin mutation on regulation of muscle contraction in single human muscle fibres.

Ochala J, Li M, Tajsharghi H, Kimber E, Tulinius M, Oldfors A, Larsson L. Ochala J, et al. Among authors: oldfors a. J Physiol. 2007 Jun 15;581(Pt 3):1283-92. doi: 10.1113/jphysiol.2007.129759. Epub 2007 Apr 12. J Physiol. 2007. PMID: 17430991 Free PMC article.

8

Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2).

Tajsharghi H, Ohlsson M, Lindberg C, Oldfors A. Tajsharghi H, et al. Among authors: oldfors a. Arch Neurol. 2007 Sep;64(9):1334-8. doi: 10.1001/archneur.64.9.1334. Arch Neurol. 2007. PMID: 17846275

9

New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations.

Ohlsson M, Quijano-Roy S, Darin N, Brochier G, Lacène E, Avila-Smirnow D, Fardeau M, Oldfors A, Tajsharghi H. Ohlsson M, et al. Among authors: oldfors a. Neurology. 2008 Dec 2;71(23):1896-901. doi: 10.1212/01.wnl.0000336654.44814.b8. Neurology. 2008. PMID: 19047562

10

TPM3 mutation in one of the original cases of cap disease.

Ohlsson M, Fidzianska A, Tajsharghi H, Oldfors A. Ohlsson M, et al. Among authors: oldfors a. Neurology. 2009 Jun 2;72(22):1961-3. doi: 10.1212/WNL.0b013e3181a82659. Neurology. 2009. PMID: 19487656 No abstract available.

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