O'Donovan DG - Search Results

1

Mitochondrial transfer RNA(Phe) mutation associated with a progressive neurodegenerative disorder characterized by psychiatric disturbance, dementia, and akinesia-rigidity.

Young TM, Blakely EL, Swalwell H, Carter JE, Kartsounis LD, O'Donovan DG, Turnbull DM, Taylor RW, de Silva RN. Young TM, et al. Arch Neurol. 2010 Nov;67(11):1399-402. doi: 10.1001/archneurol.2010.283. Arch Neurol. 2010. PMID: 21060018

2

POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease.

Harrower T, Stewart JD, Hudson G, Houlden H, Warner G, O'Donovan DG, Findlay LJ, Taylor RW, De Silva R, Chinnery PF. Harrower T, et al. Arch Neurol. 2008 Jan;65(1):133-6. doi: 10.1001/archneurol.2007.4. Arch Neurol. 2008. PMID: 18195151 Free article.

3

Early-onset cataracts, spastic paraparesis, and ataxia caused by a novel mitochondrial tRNAGlu (MT-TE) gene mutation causing severe complex I deficiency: a clinical, molecular, and neuropathologic study.

Lax NZ, Gnanapavan S, Dowson SJ, Alston CL, He L, Polvikoski TM, Jaros E, O'Donovan DG, Yarham JW, Turnbull DM, Dean AF, Taylor RW. Lax NZ, et al. J Neuropathol Exp Neurol. 2013 Feb;72(2):164-75. doi: 10.1097/NEN.0b013e31828129c5. J Neuropathol Exp Neurol. 2013. PMID: 23334599

4

Selective impairment of verb processing associated with pathological changes in Brodmann areas 44 and 45 in the motor neurone disease-dementia-aphasia syndrome.

Bak TH, O'Donovan DG, Xuereb JH, Boniface S, Hodges JR. Bak TH, et al. Brain. 2001 Jan;124(Pt 1):103-20. doi: 10.1093/brain/124.1.103. Brain. 2001. PMID: 11133791

5

TB or not TB?

Harrower T, O'Donovan D, Bavetta S, Chaudhuri A. Harrower T, et al. Am J Med. 2008 Aug;121(8):684-6. doi: 10.1016/j.amjmed.2008.01.018. Am J Med. 2008. PMID: 18691479 No abstract available.

6

Paravertebral cervical chordoma--a case report.

Bannur U, Chawda SJ, O'Donovan DG, Kaddour H, David KM. Bannur U, et al. Br J Neurosurg. 2011 Aug;25(4):527-9. doi: 10.3109/02688697.2010.508959. Epub 2010 Sep 20. Br J Neurosurg. 2011. PMID: 20854060

7

Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I).

Houlden H, King R, Blake J, Groves M, Love S, Woodward C, Hammans S, Nicoll J, Lennox G, O'Donovan DG, Gabriel C, Thomas PK, Reilly MM. Houlden H, et al. Brain. 2006 Feb;129(Pt 2):411-25. doi: 10.1093/brain/awh712. Epub 2005 Dec 19. Brain. 2006. PMID: 16364956

8

Giant intracranial hemangioma in a neonate.

Jalloh I, Dean AF, O'Donovan DG, Cross J, Garnett MR, Santarius T. Jalloh I, et al. Acta Neurochir (Wien). 2014 Jun;156(6):1151-4. doi: 10.1007/s00701-014-2007-y. Epub 2014 Feb 5. Acta Neurochir (Wien). 2014. PMID: 24497024

9

Atypical Presentation of Low-Grade Small Lymphocytic Lymphoma of the Lacrimal Sac.

Papastefanou VP, René C, O'Donovan DG, Dean AF, Wright PA. Papastefanou VP, et al. Ophthalmic Plast Reconstr Surg. 2015 Nov-Dec;31(6):e163-5. doi: 10.1097/IOP.0000000000000188. Ophthalmic Plast Reconstr Surg. 2015. PMID: 24892276

10

Wound breakdown secondary to silk granuloma 20 years after craniotomy.

Haliasos N, O'Donovan DG, Brecknell J. Haliasos N, et al. Br J Neurosurg. 2010 Aug;24(4):488-9. doi: 10.3109/02688697.2010.495167. Br J Neurosurg. 2010. PMID: 20649392

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