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Results: 1 to 20 of 35

1.

Dopamine-agonist responsive Parkinsonism in a patient with the SANDO syndrome caused by POLG mutation.

Bandettini di Poggio M, Nesti C, Bruno C, Meschini MC, Schenone A, Santorelli FM.

BMC Med Genet. 2013 Oct 7;14:105. doi: 10.1186/1471-2350-14-105.

PMID:
24099403
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Diagnostic challenges in movement disorders: Sensory Ataxia Neuropathy Dysarthria and Ophthalmoplegia (SANDO) syndrome.

Lovan A, Ihtsham ul Haq, Balakrishnan N.

BMJ Case Rep. 2013 Aug 30;2013. pii: bcr2013010343. doi: 10.1136/bcr-2013-010343.

PMID:
23997076
[PubMed - indexed for MEDLINE]
3.

Commercialization of regenerative medicine: learning from spin-outs.

French A, Buckler RL, Brindley DA.

Rejuvenation Res. 2013 Apr;16(2):164-70. doi: 10.1089/rej.2013.1423.

PMID:
23470045
[PubMed - indexed for MEDLINE]
4.

Effects of berberine gelatin on recurrent aphthous stomatitis: a randomized, placebo-controlled, double-blind trial in a Chinese cohort.

Jiang XW, Zhang Y, Zhu YL, Zhang H, Lu K, Li FF, Peng HY.

Oral Surg Oral Med Oral Pathol Oral Radiol. 2013 Feb;115(2):212-7. doi: 10.1016/j.oooo.2012.09.009. Epub 2012 Dec 12.

PMID:
23246229
[PubMed - indexed for MEDLINE]
5.

Promoting wound healing in minor recurrent aphthous stomatitis by non-thermal, non-ablative CO(2) laser therapy: a pilot study.

Zand N, Fateh M, Ataie-Fashtami L, Djavid GE, Fatemi SM, Shirkavand A.

Photomed Laser Surg. 2012 Dec;30(12):719-23. doi: 10.1089/pho.2012.3301. Epub 2012 Oct 31.

PMID:
23113511
[PubMed - indexed for MEDLINE]
6.

Early-onset ataxia with progressive external ophthalmoplegia associated with POLG mutation: autosomal recessive mitochondrial ataxic syndrome or SANDO?

Habek M, Barun B, Adamec I, Mitrović Z, Ozretić D, Brinar VV.

Neurologist. 2012 Sep;18(5):287-9. doi: 10.1097/NRL.0b013e318266f5a6.

PMID:
22931735
[PubMed - indexed for MEDLINE]
7.

Hypertrophic olivary degeneration on magnetic resonance imaging in mitochondrial syndromes associated with POLG and SURF1 mutations.

Kinghorn KJ, Kaliakatsos M, Blakely EL, Taylor RW, Rich P, Clarke A, Omer S.

J Neurol. 2013 Jan;260(1):3-9. doi: 10.1007/s00415-012-6564-9. Epub 2012 Jun 24. Review.

PMID:
22729384
[PubMed - indexed for MEDLINE]
8.

Sensory ataxic neuropathy with dysarthria/dysphagia and ophthalmoplegia (SANDO). Two case reports.

Gáti I, Danielsson O, Jonasson J, Landtblom AM.

Acta Myol. 2011 Dec;30(3):188-90.

PMID:
22616202
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Percutaneous radiofrequency ablation for malignant liver tumours in challenging locations.

Kelogrigoris M, Laspas F, Kyrkou K, Stathopoulos K, Georgiadou V, Thanos L.

J Med Imaging Radiat Oncol. 2012 Feb;56(1):48-54. doi: 10.1111/j.1754-9485.2011.02328.x.

PMID:
22339745
[PubMed - indexed for MEDLINE]
10.

Mitochondrial disease and epilepsy.

Rahman S.

Dev Med Child Neurol. 2012 May;54(5):397-406. doi: 10.1111/j.1469-8749.2011.04214.x. Epub 2012 Jan 28. Review.

PMID:
22283595
[PubMed - indexed for MEDLINE]
11.

Mitochondrial recessive ataxia syndrome mimicking dominant spinocerebellar ataxia.

Palin EJ, Hakonen AH, Korpela M, Paetau A, Suomalainen A.

J Neurol Sci. 2012 Apr 15;315(1-2):160-3. doi: 10.1016/j.jns.2011.11.028. Epub 2011 Dec 12.

PMID:
22166854
[PubMed - indexed for MEDLINE]
12.

Sleep disturbances in chronic progressive external ophthalmoplegia.

Smits BW, Westeneng HJ, van Hal MA, van Engelen BG, Overeem S.

Eur J Neurol. 2012 Jan;19(1):176-8. doi: 10.1111/j.1468-1331.2011.03496.x. Epub 2011 Aug 5.

PMID:
21819490
[PubMed - indexed for MEDLINE]
13.

MELAS/SANDO overlap syndrome associated with POLG1 mutations.

Hansen N, Zwarg T, Wanke I, Zierz S, Kastrup O, Deschauer M.

Neurol Sci. 2012 Feb;33(1):209-12. doi: 10.1007/s10072-011-0631-3. Epub 2011 Jun 7. No abstract available.

PMID:
21647632
[PubMed - indexed for MEDLINE]
14.

Inherited mitochondrial neuropathies.

Finsterer J.

J Neurol Sci. 2011 May 15;304(1-2):9-16. doi: 10.1016/j.jns.2011.02.012. Epub 2011 Mar 13. Review.

PMID:
21402391
[PubMed - indexed for MEDLINE]
15.

POLG1 manifestations in childhood.

Isohanni P, Hakonen AH, Euro L, Paetau I, Linnankivi T, Liukkonen E, Wallden T, Luostarinen L, Valanne L, Paetau A, Uusimaa J, Lönnqvist T, Suomalainen A, Pihko H.

Neurology. 2011 Mar 1;76(9):811-5. doi: 10.1212/WNL.0b013e31820e7b25.

PMID:
21357833
[PubMed - indexed for MEDLINE]
16.

Sensory ataxic neuropathy with dysarthria and ophthalmoparesis (SANDO) in late life due to compound heterozygous POLG mutations.

Weiss MD, Saneto RP.

Muscle Nerve. 2010 Jun;41(6):882-5. doi: 10.1002/mus.21636.

PMID:
20513108
[PubMed - indexed for MEDLINE]
17.

Functional analysis of H. sapiens DNA polymerase gamma spacer mutation W748S with and without common variant E1143G.

Palin EJ, Lesonen A, Farr CL, Euro L, Suomalainen A, Kaguni LS.

Biochim Biophys Acta. 2010 Jun;1802(6):545-51. doi: 10.1016/j.bbadis.2010.02.003. Epub 2010 Feb 12.

PMID:
20153822
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Mitochondrial ataxias.

Finsterer J.

Can J Neurol Sci. 2009 Sep;36(5):543-53. Review.

PMID:
19831121
[PubMed - indexed for MEDLINE]
19.

Sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO) in a sibling pair with a homozygous p.A467T POLG mutation.

McHugh JC, Lonergan R, Howley R, O'Rourke K, Taylor RW, Farrell M, Hutchinson M, Connolly S.

Muscle Nerve. 2010 Feb;41(2):265-9. doi: 10.1002/mus.21494.

PMID:
19813183
[PubMed - indexed for MEDLINE]
20.

Ataxias with autosomal, X-chromosomal or maternal inheritance.

Finsterer J.

Can J Neurol Sci. 2009 Jul;36(4):409-28. Review.

PMID:
19650351
[PubMed - indexed for MEDLINE]

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