Nicholson GA - Search Results

1

Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22-p24.

Spring PJ, Kok C, Nicholson GA, Ing AJ, Spies JM, Bassett ML, Cameron J, Kerlin P, Bowler S, Tuck R, Pollard JD. Spring PJ, et al. Among authors: nicholson ga. Brain. 2005 Dec;128(Pt 12):2797-810. doi: 10.1093/brain/awh653. Brain. 2005. PMID: 16311270

2

A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-p24.

Kok C, Kennerson ML, Spring PJ, Ing AJ, Pollard JD, Nicholson GA. Kok C, et al. Among authors: nicholson ga. Am J Hum Genet. 2003 Sep;73(3):632-7. doi: 10.1086/377591. Epub 2003 Jul 17. Am J Hum Genet. 2003. PMID: 12870133 Free PMC article.

3

RFC1 expansions can mimic hereditary sensory neuropathy with cough and Sjögren syndrome.

Kumar KR, Cortese A, Tomlinson SE, Efthymiou S, Ellis M, Zhu D, Stoll M, Dominik N, Tisch S, Tchan M, Wu KHC, Devery S, Spring PJ, Hawke S, Cremer P, Ng K, Reilly MM, Nicholson GA, Houlden H, Kennerson M. Kumar KR, et al. Among authors: nicholson ga. Brain. 2020 Oct 1;143(10):e82. doi: 10.1093/brain/awaa244. Brain. 2020. PMID: 32949124 Free PMC article. No abstract available.

4

Transcript map of the candidate region for HSNI with cough and gastroesophageal reflux on chromosome 3p and exclusion of candidate genes.

Kok C, Kennerson ML, Myers SJ, Nicholson GA. Kok C, et al. Among authors: nicholson ga. Neurogenetics. 2004 Sep;5(3):197-200. doi: 10.1007/s10048-004-0185-0. Epub 2004 Jul 6. Neurogenetics. 2004. PMID: 15241656

5

A new autosomal dominant pure cerebellar ataxia.

Storey E, Gardner RJ, Knight MA, Kennerson ML, Tuck RR, Forrest SM, Nicholson GA. Storey E, et al. Among authors: nicholson ga. Neurology. 2001 Nov 27;57(10):1913-5. doi: 10.1212/wnl.57.10.1913. Neurology. 2001. PMID: 11723290

6

CMT with pyramidal features. Charcot-Marie-Tooth.

Vucic S, Kennerson M, Zhu D, Miedema E, Kok C, Nicholson GA. Vucic S, et al. Among authors: nicholson ga. Neurology. 2003 Feb 25;60(4):696-9. doi: 10.1212/01.wnl.0000048561.61921.71. Neurology. 2003. PMID: 12601114

7

Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsies.

Sander S, Ouvrier RA, McLeod JG, Nicholson GA, Pollard JD. Sander S, et al. Among authors: nicholson ga. J Neurol Neurosurg Psychiatry. 2000 Apr;68(4):483-8. doi: 10.1136/jnnp.68.4.483. J Neurol Neurosurg Psychiatry. 2000. PMID: 10727485 Free PMC article.

8

Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy.

Silburn PA, Nicholson GA, Teh BT, Blair IP, Pollard JD, Nolan PJ, Larsson C, Boyle RS. Silburn PA, et al. Among authors: nicholson ga. Neurology. 1998 Apr;50(4):1067-73. doi: 10.1212/wnl.50.4.1067. Neurology. 1998. PMID: 9566396

9

Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations.

Vallat JM, Ouvrier RA, Pollard JD, Magdelaine C, Zhu D, Nicholson GA, Grew S, Ryan MM, Funalot B. Vallat JM, et al. Among authors: nicholson ga. J Neuropathol Exp Neurol. 2008 Nov;67(11):1097-102. doi: 10.1097/NEN.0b013e31818b6cbc. J Neuropathol Exp Neurol. 2008. PMID: 18957892

10

Charcot-Marie-Tooth disease: histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and connexin32 mutations (CMTX1).

Sander S, Nicholson GA, Ouvrier RA, McLeod JG, Pollard JD. Sander S, et al. Among authors: nicholson ga. Muscle Nerve. 1998 Feb;21(2):217-25. doi: 10.1002/(sici)1097-4598(199802)21:2<217::aid-mus9>3.0.co;2-e. Muscle Nerve. 1998. PMID: 9466597

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