Moslemi AR - Search Results

1

Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutations.

Kollberg G, Jansson M, Pérez-Bercoff A, Melberg A, Lindberg C, Holme E, Moslemi AR, Oldfors A. Kollberg G, et al. Among authors: moslemi ar. Eur J Hum Genet. 2005 Apr;13(4):463-9. doi: 10.1038/sj.ejhg.5201341. Eur J Hum Genet. 2005. PMID: 15702133

2

Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit I.

Kollberg G, Moslemi AR, Lindberg C, Holme E, Oldfors A. Kollberg G, et al. Among authors: moslemi ar. J Neuropathol Exp Neurol. 2005 Feb;64(2):123-8. doi: 10.1093/jnen/64.2.123. J Neuropathol Exp Neurol. 2005. PMID: 15751226

3

POLG1 mutations associated with progressive encephalopathy in childhood.

Kollberg G, Moslemi AR, Darin N, Nennesmo I, Bjarnadottir I, Uvebrant P, Holme E, Melberg A, Tulinius M, Oldfors A. Kollberg G, et al. Among authors: moslemi ar. J Neuropathol Exp Neurol. 2006 Aug;65(8):758-68. doi: 10.1097/01.jnen.0000229987.17548.6e. J Neuropathol Exp Neurol. 2006. PMID: 16896309

4

A patient with two mitochondrial DNA mutations causing PEO and LHON.

Melberg A, Moslemi AR, Palm O, Raininko R, Stålberg E, Oldfors A. Melberg A, et al. Among authors: moslemi ar. Eur J Med Genet. 2009 Jan-Feb;52(1):47-8. doi: 10.1016/j.ejmg.2008.10.004. Epub 2008 Nov 5. Eur J Med Genet. 2009. PMID: 19015050

5

A novel mitochondrial tRNA Arg mutation resulting in an anticodon swap in a patient with mitochondrial encephalomyopathy.

Roos S, Darin N, Kollberg G, Andersson Grönlund M, Tulinius M, Holme E, Moslemi AR, Oldfors A. Roos S, et al. Among authors: moslemi ar. Eur J Hum Genet. 2013 May;21(5):571-3. doi: 10.1038/ejhg.2012.153. Epub 2012 Jul 11. Eur J Hum Genet. 2013. PMID: 22781096 Free PMC article.

6

Subnormal levels of POLγA cause inefficient initiation of light-strand DNA synthesis and lead to mitochondrial DNA deletions and progressive external ophthalmoplegia [corrected].

Roos S, Macao B, Fusté JM, Lindberg C, Jemt E, Holme E, Moslemi AR, Oldfors A, Falkenberg M. Roos S, et al. Among authors: moslemi ar. Hum Mol Genet. 2013 Jun 15;22(12):2411-22. doi: 10.1093/hmg/ddt094. Epub 2013 Feb 27. Hum Mol Genet. 2013. PMID: 23446635

7

Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia.

Moslemi AR, Melberg A, Holme E, Oldfors A. Moslemi AR, et al. Ann Neurol. 1996 Nov;40(5):707-13. doi: 10.1002/ana.410400506. Ann Neurol. 1996. PMID: 8957011

8

Analysis of multiple mitochondrial DNA deletions in inclusion body myositis.

Moslemi AR, Lindberg C, Oldfors A. Moslemi AR, et al. Hum Mutat. 1997;10(5):381-6. doi: 10.1002/(SICI)1098-1004(1997)10:5<381::AID-HUMU8>3.0.CO;2-I. Hum Mutat. 1997. PMID: 9375854

9

A novel heteroplasmic point mutation in the mitochondrial tRNA(Lys) gene in a sporadic case of mitochondrial encephalomyopathy: de novo mutation and no transmission to the offspring.

Houshmand M, Lindberg C, Moslemi AR, Oldfors A, Holme E. Houshmand M, et al. Among authors: moslemi ar. Hum Mutat. 1999;13(3):203-9. doi: 10.1002/(SICI)1098-1004(1999)13:3<203::AID-HUMU4>3.0.CO;2-3. Hum Mutat. 1999. PMID: 10090475

10

Autosomal dominant progressive external ophthalmoplegia: distribution of multiple mitochondrial DNA deletions.

Moslemi AR, Melberg A, Holme E, Oldfors A. Moslemi AR, et al. Neurology. 1999 Jul 13;53(1):79-84. doi: 10.1212/wnl.53.1.79. Neurology. 1999. PMID: 10408540

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