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Similar articles for PubMed (Select 24014582)

1.

Progressive external ophthalmoplegia (PEO) due to a mutation in the C10orf2 (PEO1) gene mimicking a myasthenic crisis.

Gonzalez-Moron D, Bueri J, Kauffman MA.

BMJ Case Rep. 2013 Sep 7;2013. pii: bcr2013010181. doi: 10.1136/bcr-2013-010181.

PMID:
24014582
2.

Myasthenia gravis mimicking stroke: a case series with sudden onset dysarthria.

Tremolizzo L, Giopato F, Piatti ML, Rigamonti A, Ferrarese C, Appollonio I.

Neurol Sci. 2015 Jun;36(6):895-8. doi: 10.1007/s10072-015-2098-0. Epub 2015 Feb 4.

PMID:
25648108
3.

Myasthenia Gravis following Low-Osmolality Iodinated Contrast Media.

Bonanni L, Dalla Vestra M, Zancanaro A, Presotto F.

Case Rep Radiol. 2014;2014:963461. doi: 10.1155/2014/963461. Epub 2014 Dec 3.

4.

Myasthenia gravis masquerading as dysphagia: unveiled by magnesium infusion.

Klair JS, Rochlani YM, Meena NK.

BMJ Case Rep. 2014 Apr 17;2014. pii: bcr2014204163. doi: 10.1136/bcr-2014-204163.

PMID:
24744075
5.

Horizontal gaze palsy with progressive scoliosis in a Moroccan family.

Handor H, Laghmari M, Hafidi Z, Daoudi R.

Orthop Traumatol Surg Res. 2014 Apr;100(2):255-7. doi: 10.1016/j.otsr.2013.08.012. Epub 2014 Feb 20.

PMID:
24559884
6.

Twinkle mutations in two Chinese families with autosomal dominant progressive external ophthalmoplegia.

Ji K, Liu K, Lin P, Wen B, Luo YB, Zhao Y, Yan C.

Neurol Sci. 2014 Mar;35(3):443-8. doi: 10.1007/s10072-013-1557-8. Epub 2013 Oct 4.

PMID:
24091712
7.

Twinkle mutation in an Italian family with external progressive ophthalmoplegia and parkinsonism: a case report and an update on the state of art.

Kiferle L, Orsucci D, Mancuso M, Lo Gerfo A, Petrozzi L, Siciliano G, Ceravolo R, Bonuccelli U.

Neurosci Lett. 2013 Nov 27;556:1-4. doi: 10.1016/j.neulet.2013.09.034. Epub 2013 Sep 26. Review.

PMID:
24076137
8.

Orthostatic tremor, progressive external ophthalmoplegia, and Twinkle.

Milone M, Klassen BT, Landsverk ML, Haas RH, Wong LJ.

JAMA Neurol. 2013 Nov;70(11):1429-31. doi: 10.1001/jamaneurol.2013.3521.

PMID:
24061067
9.

Longitudinal clinical follow-up of a large family with the R357P Twinkle mutation.

Paradas C, Camaño P, Otaegui D, Oz O, Emmanuele V, DiMauro S, Hirano M.

JAMA Neurol. 2013 Nov;70(11):1425-8. doi: 10.1001/jamaneurol.2013.3185.

10.

Autosomal dominant mutations in POLG and C10orf2: association with late onset chronic progressive external ophthalmoplegia and Parkinsonism in two patients.

Brandon BR, Diederich NJ, Soni M, Witte K, Weinhold M, Krause M, Jackson S.

J Neurol. 2013 Jul;260(7):1931-3. doi: 10.1007/s00415-013-6975-2. Epub 2013 May 30. No abstract available.

PMID:
23719791
11.

What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?

Neeve VC, Samuels DC, Bindoff LA, van den Bosch B, Van Goethem G, Smeets H, Lombès A, Jardel C, Hirano M, Dimauro S, De Vries M, Smeitink J, Smits BW, de Coo IF, Saft C, Klopstock T, Keiling BC, Czermin B, Abicht A, Lochmüller H, Hudson G, Gorman GG, Turnbull DM, Taylor RW, Holinski-Feder E, Chinnery PF, Horvath R.

Brain. 2012 Dec;135(Pt 12):3614-26. doi: 10.1093/brain/aws298.

12.

Miller Fisher syndrome mimicking ocular myasthenia gravis.

Anthony SA, Thurtell MJ, Leigh RJ.

Optom Vis Sci. 2012 Dec;89(12):e118-23. doi: 10.1097/OPX.0b013e31827717c1.

13.

Cardiac screening investigations in adult-onset progressive external ophthalmoplegia patients.

Pfeffer G, Mezei MM.

Muscle Nerve. 2012 Oct;46(4):593-6. doi: 10.1002/mus.23538. Review.

PMID:
22987704
14.

[A clinical test for diagnosis of myasthenic ptosis].

Likhachev SA, Kulikova SL.

Zh Nevrol Psikhiatr Im S S Korsakova. 2012;112(5):18-21. Russian.

PMID:
22951776
15.

Novel POLG1 mutations in a patient with adult-onset progressive external ophthalmoplegia and encephalopathy.

Martikainen MH, Hinttala R, Majamaa K.

BMJ Case Rep. 2010 Sep 29;2010. pii: bcr0120102604. doi: 10.1136/bcr.01.2010.2604.

16.

Levator palpebrae biopsy and diagnosis of progressive external ophthalmoplegia.

Pfeffer G, Waters PJ, Maguire J, Vallance HD, Wong VA, Mezei MM.

Can J Neurol Sci. 2012 Jul;39(4):520-4.

PMID:
22728862
17.

Progressive external ophthalmoplegia in southwestern Finland: a clinical and genetic study.

Martikainen MH, Hinttala R, Röyttä M, Jääskeläinen S, Wendelin-Saarenhovi M, Parkkola R, Majamaa K.

Neuroepidemiology. 2012;38(2):114-9. doi: 10.1159/000336112. Epub 2012 Feb 24.

PMID:
22377773
18.

A new mitochondrial point mutation in the transfer RNA(Lys) gene associated with progressive external ophthalmoplegia with impaired respiratory regulation.

Wolf J, Obermaier-Kusser B, Jacobs M, Milles C, Mörl M, von Pein HD, Grau AJ, Bauer MF.

J Neurol Sci. 2012 May 15;316(1-2):108-11. doi: 10.1016/j.jns.2012.01.013. Epub 2012 Feb 10.

PMID:
22326363
19.

Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia.

Takata A, Kato M, Nakamura M, Yoshikawa T, Kanba S, Sano A, Kato T.

Genome Biol. 2011 Sep 28;12(9):R92. doi: 10.1186/gb-2011-12-9-r92.

20.

Thymidine kinase 2 mutations in autosomal recessive progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.

Tyynismaa H, Sun R, Ahola-Erkkilä S, Almusa H, Pöyhönen R, Korpela M, Honkaniemi J, Isohanni P, Paetau A, Wang L, Suomalainen A.

Hum Mol Genet. 2012 Jan 1;21(1):66-75. doi: 10.1093/hmg/ddr438. Epub 2011 Sep 21.

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