Hardiman O - Search Results

1

A novel MYH7 Leu1453pro mutation resulting in Laing distal myopathy in an Irish family.

Lefter S, Hardiman O, McLaughlin RL, Murphy SM, Farrell M, Ryan AM. Lefter S, et al. Among authors: hardiman o. Neuromuscul Disord. 2015 Feb;25(2):155-60. doi: 10.1016/j.nmd.2014.09.007. Epub 2014 Sep 28. Neuromuscul Disord. 2015. PMID: 25447691

2

Microdysgenesis in resected temporal neocortex: incidence and clinical significance in focal epilepsy.

Hardiman O, Burke T, Phillips J, Murphy S, O'Moore B, Staunton H, Farrell MA. Hardiman O, et al. Among authors: o moore b. Neurology. 1988 Jul;38(7):1041-7. doi: 10.1212/wnl.38.7.1041. Neurology. 1988. PMID: 3386820

3

Dystrophin deficiency, altered cell signalling and fibre hypertrophy.

Hardiman O. Hardiman O. Neuromuscul Disord. 1994 Jul;4(4):305-15. doi: 10.1016/0960-8966(94)90066-3. Neuromuscul Disord. 1994. PMID: 7981587 Review.

4

Neuropathic findings in oculopharyngeal muscular dystrophy. A report of seven cases and a review of the literature.

Hardiman O, Halperin JJ, Farrell MA, Shapiro BE, Wray SH, Brown RH Jr. Hardiman O, et al. Arch Neurol. 1993 May;50(5):481-8. doi: 10.1001/archneur.1993.00540050033011. Arch Neurol. 1993. PMID: 8387769

5

Inflammatory myopathy in thyrotoxicosis.

Hardiman O, Molloy F, Brett F, Farrell M. Hardiman O, et al. Neurology. 1997 Feb;48(2):339-41. doi: 10.1212/wnl.48.2.339. Neurology. 1997. PMID: 9040717

6

Paramyotonia congenita and hyperkalemic periodic paralysis associated with a Met 1592 Val substitution in the skeletal muscle sodium channel alpha subunit--a large kindred with a novel phenotype.

Kelly P, Yang WS, Costigan D, Farrell MA, Murphy S, Hardiman O. Kelly P, et al. Among authors: hardiman o. Neuromuscul Disord. 1997 Mar;7(2):105-11. doi: 10.1016/s0960-8966(96)00429-4. Neuromuscul Disord. 1997. PMID: 9131651

7

Leptospire-induced acute rhabdomyolysis in a patient with previously undiagnosed mitochondrial myopathy.

Duran S, Hardiman O, Farrell M, O'Connor KG. Duran S, et al. Among authors: hardiman o, o connor kg. Ir Med J. 2000 Sep;93(6):182-3. Ir Med J. 2000. PMID: 11105443 No abstract available.

8

Polymyositis masquerading as motor neuron disease.

Ryan A, Nor AM, Costigan D, Foley-Nolan D, El-Rafie A, Farrell MA, Hardiman O. Ryan A, et al. Among authors: hardiman o. Arch Neurol. 2003 Jul;60(7):1001-3. doi: 10.1001/archneur.60.7.1001. Arch Neurol. 2003. PMID: 12873858

9

Intracranial giant cell arteritis with fatal middle cerebral artery territory infarct.

Browne L, Hardiman O, O'Dwyer H, Farrell M. Browne L, et al. Among authors: o dwyer h, hardiman o. Clin Neuropathol. 2003 Jul-Aug;22(4):199-203. Clin Neuropathol. 2003. PMID: 12908757

10

Sonographically guided percutaneous muscle biopsy in diagnosis of neuromuscular disease: a useful alternative to open surgical biopsy.

O'Sullivan PJ, Gorman GM, Hardiman OM, Farrell MJ, Logan PM. O'Sullivan PJ, et al. Among authors: hardiman om. J Ultrasound Med. 2006 Jan;25(1):1-6. doi: 10.7863/jum.2006.25.1.1. J Ultrasound Med. 2006. PMID: 16371549

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