Kneebone CS - Search Results

1

The causes of sporadic and 'senile' chorea.

Warren JD, Firgaira F, Thompson EM, Kneebone CS, Blumbergs PC, Thompson PD. Warren JD, et al. Among authors: kneebone cs. Aust N Z J Med. 1998 Aug;28(4):429-31. doi: 10.1111/j.1445-5994.1998.tb02075.x. Aust N Z J Med. 1998. PMID: 9777108

2

Chorea, transverse myelitis, neuropathy and a distinctive MRI: paraneoplastic manifestations of probable small cell lung cancer.

Kleinig TJ, Thompson PD, Kneebone CS. Kleinig TJ, et al. Among authors: kneebone cs. J Clin Neurosci. 2009 Jul;16(7):964-6. doi: 10.1016/j.jocn.2008.08.041. Epub 2009 Mar 28. J Clin Neurosci. 2009. PMID: 19329321

3

The distinctive movement disorder of ovarian teratoma-associated encephalitis.

Kleinig TJ, Thompson PD, Matar W, Duggins A, Kimber TE, Morris JG, Kneebone CS, Blumbergs PC. Kleinig TJ, et al. Among authors: kneebone cs. Mov Disord. 2008 Jul 15;23(9):1256-61. doi: 10.1002/mds.22073. Mov Disord. 2008. PMID: 18442127

4

Localized hypertrophic neuropathy: a case report and review of the literature.

Koszyca B, Jones N, Kneebone C, Blumbergs P. Koszyca B, et al. Clin Neuropathol. 2009 Jan-Feb;28(1):54-8. doi: 10.5414/npp28054. Clin Neuropathol. 2009. PMID: 19216221

5

Myoclonus in spinal dysraphism.

Warren JE, Vidailhet M, Kneebone CS, Quinn NP, Thompson PD. Warren JE, et al. Among authors: kneebone cs. Mov Disord. 2003 Aug;18(8):961-4. doi: 10.1002/mds.10469. Mov Disord. 2003. PMID: 12889092

6

Non-coding VMA21 deletions cause X-linked myopathy with excessive autophagy.

Ruggieri A, Ramachandran N, Wang P, Haan E, Kneebone C, Manavis J, Morandi L, Moroni I, Blumbergs P, Mora M, Minassian BA. Ruggieri A, et al. Neuromuscul Disord. 2015 Mar;25(3):207-11. doi: 10.1016/j.nmd.2014.11.014. Epub 2014 Nov 26. Neuromuscul Disord. 2015. PMID: 25683699

7

Unusual focal dyskinesias: the ears, the shoulders, the back, and the abdomen.

Caviness JN, Gabellini A, Kneebone CS, Thompson PD, Lees AJ, Marsden CD. Caviness JN, et al. Among authors: kneebone cs. Mov Disord. 1994 Sep;9(5):531-8. doi: 10.1002/mds.870090505. Mov Disord. 1994. PMID: 7990848

8

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1.

Laing NG, Wilton SD, Akkari PA, Dorosz S, Boundy K, Kneebone C, Blumbergs P, White S, Watkins H, Love DR, et al. Laing NG, et al. Nat Genet. 1995 Jun;10(2):249. doi: 10.1038/ng0695-249. Nat Genet. 1995. PMID: 7663526 No abstract available.

9

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy.

Laing NG, Wilton SD, Akkari PA, Dorosz S, Boundy K, Kneebone C, Blumbergs P, White S, Watkins H, Love DR, et al. Laing NG, et al. Nat Genet. 1995 Jan;9(1):75-9. doi: 10.1038/ng0195-75. Nat Genet. 1995. PMID: 7704029

10

Rendu-Osler-Weber syndrome: a current perspective on cerebral manifestations.

McDonald MJ, Brophy BP, Kneebone C. McDonald MJ, et al. J Clin Neurosci. 1998 Jul;5(3):345-50. doi: 10.1016/s0967-5868(98)90076-5. J Clin Neurosci. 1998. PMID: 18639047

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