Ohlsson M - Search Results

1

Hereditary myopathy with early respiratory failure associated with a mutation in A-band titin.

Ohlsson M, Hedberg C, Brådvik B, Lindberg C, Tajsharghi H, Danielsson O, Melberg A, Udd B, Martinsson T, Oldfors A. Ohlsson M, et al. Brain. 2012 Jun;135(Pt 6):1682-94. doi: 10.1093/brain/aws103. Epub 2012 May 9. Brain. 2012. PMID: 22577218

2

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. Neurology. 2008 Dec 2;71(23):1896-901. doi: 10.1212/01.wnl.0000336654.44814.b8. Neurology. 2008. PMID: 19047562

3

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

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

4

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: ohlsson m. Arch Neurol. 2007 Sep;64(9):1334-8. doi: 10.1001/archneur.64.9.1334. Arch Neurol. 2007. PMID: 17846275

5

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. Neuromuscul Disord. 2004 Sep;14(8-9):471-5. doi: 10.1016/j.nmd.2004.05.016. Neuromuscul Disord. 2004. PMID: 15336687

6

Mitochondrial abnormalities in inclusion-body myositis.

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

7

Myopathies associated with β-tropomyosin mutations.

Tajsharghi H, Ohlsson M, Palm L, Oldfors A. Tajsharghi H, et al. Among authors: ohlsson m. Neuromuscul Disord. 2012 Nov;22(11):923-33. doi: 10.1016/j.nmd.2012.05.018. Epub 2012 Jun 29. Neuromuscul Disord. 2012. PMID: 22749895 Review.

8

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: ohlsson m. 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.

9

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

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

10

[Group dialogues with students during the 11th semester. Coordination of training of consultation skills is missing].

Hedberg C, Hensjö LO, Ohlsson M, Furhoff AK. Hedberg C, et al. Among authors: ohlsson m. Lakartidningen. 2001 Nov 21;98(47):5378, 5381. Lakartidningen. 2001. PMID: 11763640 Swedish. No abstract available.

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