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Items: 1 to 50 of 63

1.

Ataxia-telangiectasia-like disorder in a family deficient for MRE11A, caused by a MRE11 variant.

Sedghi M, Salari M, Moslemi AR, Kariminejad A, Davis M, Goullée H, Olsson B, Laing N, Tajsharghi H.

Neurol Genet. 2018 Dec 3;4(6):e295. doi: 10.1212/NXG.0000000000000295. eCollection 2018 Dec.

2.

Genera of phytopathogenic fungi: GOPHY 2.

Marin-Felix Y, Hernández-Restrepo M, Wingfield MJ, Akulov A, Carnegie AJ, Cheewangkoon R, Gramaje D, Groenewald JZ, Guarnaccia V, Halleen F, Lombard L, Luangsa-Ard J, Marincowitz S, Moslemi A, Mostert L, Quaedvlieg W, Schumacher RK, Spies CFJ, Thangavel R, Taylor PWJ, Wilson AM, Wingfield BD, Wood AR, Crous PW.

Stud Mycol. 2019 Mar;92:47-133. doi: 10.1016/j.simyco.2018.04.002. Epub 2018 May 1.

3.

Translation and Psychometric Properties of the Copenhagen Burnout Inventory in Iranian Nurses.

Mahmoudi S, Atashzadeh-Shoorideh F, Rassouli M, Moslemi A, Pishgooie AH, Azimi H.

Iran J Nurs Midwifery Res. 2017 Mar-Apr;22(2):117-122. doi: 10.4103/1735-9066.205958.

4.

Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1.

Darin N, Hedberg-Oldfors C, Kroksmark AK, Moslemi AR, Kollberg G, Oldfors A.

Eur J Neurol. 2017 Apr;24(4):587-593. doi: 10.1111/ene.13249. Epub 2017 Feb 9.

PMID:
28181352
5.

Paraphoma Crown Rot of Pyrethrum (Tanacetum cinerariifolium).

Moslemi A, Ades PK, Groom T, Crous PW, Nicolas ME, Taylor PWJ.

Plant Dis. 2016 Dec;100(12):2363-2369. doi: 10.1094/PDIS-05-16-0628-RE. Epub 2016 Sep 30.

PMID:
30686162
6.

Prevalence of antibodies to a new histo-blood system: the FORS system.

Jesus C, Hesse C, Rocha C, Osório N, Valado A, Caseiro A, Gabriel A, Svensson L, Moslemi AR, Siba WA, Srour MA, Pereira C, Tomaz J, Teixeira P, Mendes F.

Blood Transfus. 2018 Feb;16(2):178-183. doi: 10.2450/2016.0120-16. Epub 2016 Oct 24.

7.

Histopathological changes in skeletal muscle associated with chronic ischaemia.

Roos S, Fyhr IM, Sunnerhagen KS, Moslemi AR, Oldfors A, Ullman M.

APMIS. 2016 Nov;124(11):935-941. doi: 10.1111/apm.12586. Epub 2016 Aug 19.

PMID:
27539941
8.

Truncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndrome.

Kariminejad A, Almadani N, Khoshaeen A, Olsson B, Moslemi AR, Tajsharghi H.

BMC Genet. 2016 May 31;17(1):71. doi: 10.1186/s12863-016-0382-5.

9.

Lethal multiple pterygium syndrome, the extreme end of the RYR1 spectrum.

Kariminejad A, Ghaderi-Sohi S, Hossein-Nejad Nedai H, Varasteh V, Moslemi AR, Tajsharghi H.

BMC Musculoskelet Disord. 2016 Mar 1;17:109. doi: 10.1186/s12891-016-0947-5.

10.

Bayesian Survival Analysis of High-Dimensional Microarray Data for Mantle Cell Lymphoma Patients.

Moslemi A, Mahjub H, Saidijam M, Poorolajal J, Soltanian AR.

Asian Pac J Cancer Prev. 2016;17(1):95-100.

11.

Developmental MYH3 Myopathy Associated with Expression of Mutant Protein and Reduced Expression Levels of Embryonic MyHC.

Pokrzywa M, Norum M, Lengqvist J, Ghobadpour M, Abdul-Hussein S, Moslemi AR, Tajsharghi H.

PLoS One. 2015 Nov 6;10(11):e0142094. doi: 10.1371/journal.pone.0142094. eCollection 2015.

12.

Mitochondrial pathology in inclusion body myositis.

Lindgren U, Roos S, Hedberg Oldfors C, Moslemi AR, Lindberg C, Oldfors A.

Neuromuscul Disord. 2015 Apr;25(4):281-8. doi: 10.1016/j.nmd.2014.12.010. Epub 2015 Jan 6.

PMID:
25638290
13.

Broad phenotypic variability in patients with complex I deficiency due to mutations in NDUFS1 and NDUFV1.

Björkman K, Sofou K, Darin N, Holme E, Kollberg G, Asin-Cayuela J, Holmberg Dahle KM, Oldfors A, Moslemi AR, Tulinius M.

Mitochondrion. 2015 Mar;21:33-40. doi: 10.1016/j.mito.2015.01.003. Epub 2015 Jan 20.

PMID:
25615419
14.

Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations.

Roos S, Lindgren U, Ehrstedt C, Moslemi AR, Oldfors A.

Neuromuscul Disord. 2014 Aug;24(8):713-20. doi: 10.1016/j.nmd.2014.05.009. Epub 2014 May 29.

PMID:
24953930
15.

LC-MS/MS characterization of combined glycogenin-1 and glycogenin-2 enzymatic activities reveals their self-glucosylation preferences.

Nilsson J, Halim A, Larsson E, Moslemi AR, Oldfors A, Larson G, Nilsson J.

Biochim Biophys Acta. 2014 Feb;1844(2):398-405. doi: 10.1016/j.bbapap.2013.11.002. Epub 2013 Nov 14.

PMID:
24239874
16.

Phenotypes of myopathy-related beta-tropomyosin mutants in human and mouse tissue cultures.

Abdul-Hussein S, Rahl K, Moslemi AR, Tajsharghi H.

PLoS One. 2013 Sep 10;8(9):e72396. doi: 10.1371/journal.pone.0072396. eCollection 2013.

17.

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.

Hum Mol Genet. 2013 Jun 15;22(12):2411-22. doi: 10.1093/hmg/ddt094. Epub 2013 Feb 27. Erratum in: Hum Mol Genet. 2013 Dec 20;22(25):5295.

PMID:
23446635
18.

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.

Eur J Hum Genet. 2013 May;21(5):571-3. doi: 10.1038/ejhg.2012.153. Epub 2012 Jul 11.

19.

Phenotypic and genotypic variability in Alpers syndrome.

Sofou K, Moslemi AR, Kollberg G, Bjarnadóttir I, Oldfors A, Nennesmo I, Holme E, Tulinius M, Darin N.

Eur J Paediatr Neurol. 2012 Jul;16(4):379-89. doi: 10.1016/j.ejpn.2011.12.006. Epub 2012 Jan 10.

PMID:
22237560
20.

Molecular pathogenesis of a new glycogenosis caused by a glycogenin-1 mutation.

Nilsson J, Halim A, Moslemi AR, Pedersen A, Nilsson J, Larson G, Oldfors A.

Biochim Biophys Acta. 2012 Apr;1822(4):493-9. doi: 10.1016/j.bbadis.2011.11.017. Epub 2011 Dec 9.

21.

Myopathy in a woman and her daughter associated with a novel splice site MTM1 mutation.

Hedberg C, Lindberg C, Máthé G, Moslemi AR, Oldfors A.

Neuromuscul Disord. 2012 Mar;22(3):244-51. doi: 10.1016/j.nmd.2011.10.010. Epub 2011 Nov 18.

PMID:
22101172
22.

The effect of Reynolds number on the propulsive efficiency of a biomorphic pulsed-jet underwater vehicle.

Moslemi AA, Krueger PS.

Bioinspir Biomim. 2011 Jun;6(2):026001. doi: 10.1088/1748-3182/6/2/026001. Epub 2011 Mar 1.

PMID:
21364256
23.

Propulsive efficiency of a biomorphic pulsed-jet underwater vehicle.

Moslemi AA, Krueger PS.

Bioinspir Biomim. 2010 Sep;5(3):036003. doi: 10.1088/1748-3182/5/3/036003. Epub 2010 Aug 16.

PMID:
20710067
24.

Ophthalmological findings in children and young adults with genetically verified mitochondrial disease.

Grönlund MA, Honarvar AK, Andersson S, Moslemi AR, Oldfors A, Holme E, Tulinius M, Darin N.

Br J Ophthalmol. 2010 Jan;94(1):121-7. doi: 10.1136/bjo.2008.154187.

PMID:
20385529
25.

Glycogenin-1 deficiency and inactivated priming of glycogen synthesis.

Moslemi AR, Lindberg C, Nilsson J, Tajsharghi H, Andersson B, Oldfors A.

N Engl J Med. 2010 Apr 1;362(13):1203-10. doi: 10.1056/NEJMoa0900661.

26.

Fournier gangrene presenting in a patient with undiagnosed rectal adenocarcinoma: a case report.

Moslemi MK, Sadighi Gilani MA, Moslemi AA, Arabshahi A.

Cases J. 2009 Dec 3;2:9136. doi: 10.1186/1757-1626-2-9136.

27.

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.

Horvath R, Kemp JP, Tuppen HA, Hudson G, Oldfors A, Marie SK, Moslemi AR, Servidei S, Holme E, Shanske S, Kollberg G, Jayakar P, Pyle A, Marks HM, Holinski-Feder E, Scavina M, Walter MC, Coku J, Günther-Scholz A, Smith PM, McFarland R, Chrzanowska-Lightowlers ZM, Lightowlers RN, Hirano M, Lochmüller H, Taylor RW, Chinnery PF, Tulinius M, DiMauro S.

Brain. 2009 Nov;132(Pt 11):3165-74. doi: 10.1093/brain/awp221. Epub 2009 Aug 31.

28.

A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion.

Kollberg G, Darin N, Benan K, Moslemi AR, Lindal S, Tulinius M, Oldfors A, Holme E.

Neuromuscul Disord. 2009 Feb;19(2):147-50. doi: 10.1016/j.nmd.2008.11.014. Epub 2009 Jan 12.

PMID:
19138848
29.

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

Melberg A, Moslemi AR, Palm O, Raininko R, Stålberg E, Oldfors A.

Eur J Med Genet. 2009 Jan-Feb;52(1):47-8. doi: 10.1016/j.ejmg.2008.10.004. Epub 2008 Nov 5.

PMID:
19015050
30.

Progressive encephalopathy and complex I deficiency associated with mutations in MTND1.

Moslemi AR, Darin N, Tulinius M, Wiklund LM, Holme E, Oldfors A.

Neuropediatrics. 2008 Feb;39(1):24-8. doi: 10.1055/s-2008-1076739.

PMID:
18504678
31.

MELAS syndrome in a patient with a point mutation in MTTS1.

Lindberg C, Moslemi AR, Oldfors A.

Acta Neurol Scand. 2008 Feb;117(2):128-32. Epub 2007 Sep 25.

PMID:
17894844
32.

Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I.

Darin N, Kroksmark AK, Ahlander AC, Moslemi AR, Oldfors A, Tulinius M.

Eur J Paediatr Neurol. 2007 Nov;11(6):353-7. Epub 2007 Apr 18.

PMID:
17446099
33.

Molecular genetic and clinical aspects of mitochondrial disorders in childhood.

Moslemi AR, Darin N.

Mitochondrion. 2007 Jul;7(4):241-52. Epub 2007 Feb 14. Review.

PMID:
17376748
34.

A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intolerance.

Mayr JA, Moslemi AR, Förster H, Kamper A, Idriceanu C, Muss W, Huemer M, Oldfors A, Sperl W.

Neuromuscul Disord. 2006 Dec;16(12):874-7. Epub 2006 Oct 20.

PMID:
17056256
35.

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.

J Neuropathol Exp Neurol. 2006 Aug;65(8):758-68.

PMID:
16896309
36.

A Western blot and molecular genetic investigation of the estrogen receptor beta in giant cell arteritis.

Larsson K, Nordborg C, Moslemi AR, Nordborg E.

Clin Exp Rheumatol. 2006 Mar-Apr;24(2 Suppl 41):S17-9.

PMID:
16859590
37.

Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNA(phe) gene.

Darin N, Kollberg G, Moslemi AR, Tulinius M, Holme E, Grönlund MA, Andersson S, Oldfors A.

Neuromuscul Disord. 2006 Aug;16(8):504-6. Epub 2006 Jun 27.

PMID:
16806928
38.

Mitochondrial abnormalities in inclusion-body myositis.

Oldfors A, Moslemi AR, Jonasson L, Ohlsson M, Kollberg G, Lindberg C.

Neurology. 2006 Jan 24;66(2 Suppl 1):S49-55. Review.

PMID:
16432145
39.

Two new mutations in the MTATP6 gene associated with Leigh syndrome.

Moslemi AR, Darin N, Tulinius M, Oldfors A, Holme E.

Neuropediatrics. 2005 Oct;36(5):314-8.

PMID:
16217706
40.

Alzheimer pathology associated with POLG1 mutation, multiple mtDNA deletions, and APOE4/4: premature ageing or just coincidence?

Melberg A, Nennesmo I, Moslemi AR, Kollberg G, Luoma P, Suomalainen A, Holme E, Oldfors A.

Acta Neuropathol. 2005 Sep;110(3):315-6. Epub 2005 Jun 25. No abstract available.

PMID:
15981013
41.

Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletion.

Tulinius M, Moslemi AR, Darin N, Holme E, Oldfors A.

Neuromuscul Disord. 2005 Jun;15(6):412-5.

PMID:
15907288
42.

Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.

Kärppä M, Herva R, Moslemi AR, Oldfors A, Kakko S, Majamaa K.

Brain. 2005 Aug;128(Pt 8):1861-9. Epub 2005 Apr 27.

PMID:
15857931
43.

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.

J Neuropathol Exp Neurol. 2005 Feb;64(2):123-8.

PMID:
15751226
44.

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.

Eur J Hum Genet. 2005 Apr;13(4):463-9.

45.

Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency.

Darin N, Moslemi AR, Lebon S, Rustin P, Holme E, Oldfors A, Tulinius M.

Neuropediatrics. 2003 Dec;34(6):311-7. Review.

PMID:
14681757
46.

A novel mutation in the mitochondrial tRNA(Phe) gene associated with mitochondrial myopathy.

Moslemi AR, Lindberg C, Toft J, Holme E, Kollberg G, Oldfors A.

Neuromuscul Disord. 2004 Jan;14(1):46-50.

PMID:
14659412
47.

SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiency.

Moslemi AR, Tulinius M, Darin N, Aman P, Holme E, Oldfors A.

Neurology. 2003 Oct 14;61(7):991-3.

PMID:
14557577
48.

Inclusion body myositis: clonal expansions of muscle-infiltrating T cells persist over time.

Müntzing K, Lindberg C, Moslemi AR, Oldfors A.

Scand J Immunol. 2003 Aug;58(2):195-200.

49.

Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene.

Tulinius M, Moslemi AR, Darin N, Westerberg B, Wiklund LM, Holme E, Oldfors A.

Neuropediatrics. 2003 Apr;34(2):87-91.

PMID:
12776230
50.

Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function.

Fayet G, Jansson M, Sternberg D, Moslemi AR, Blondy P, Lombès A, Fardeau M, Oldfors A.

Neuromuscul Disord. 2002 Jun;12(5):484-93.

PMID:
12031622

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