Nicholson GA - Search Results

1

Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice.

McCann EP, Fifita JA, Grima N, Galper J, Mehta P, Freckleton SE, Zhang KY, Henden L, Hogan AL, Chan Moi Fat S, Wu SS, Jagaraj CJ, Berning BA, Williams KL, Twine NA, Bauer D, Piguet O, Hodges J, Kwok JBJ, Halliday GM, Kiernan MC, Atkin J, Rowe DB, Nicholson GA, Walker AK, Blair IP, Yang S. McCann EP, et al. Among authors: nicholson ga. J Neurol Neurosurg Psychiatry. 2020 Feb;91(2):162-171. doi: 10.1136/jnnp-2019-321790. Epub 2019 Nov 5. J Neurol Neurosurg Psychiatry. 2020. PMID: 31690696

2

Single test for two hereditary neuropathies, CMT1A and HNPP.

Kennerson ML, Gordon MJ, Blair IP, Nicholson GA. Kennerson ML, et al. Among authors: nicholson ga. Clin Chem. 1995 Oct;41(10):1534-5. Clin Chem. 1995. PMID: 7586531 No abstract available.

3

Detection of Charcot-Marie-Tooth type 1A duplication by the polymerase chain reaction.

Blair IP, Kennerson ML, Nicholson GA. Blair IP, et al. Among authors: nicholson ga. Clin Chem. 1995 Aug;41(8 Pt 1):1105-8. Clin Chem. 1995. PMID: 7628084

4

Prevalence and origin of de novo duplications in Charcot-Marie-Tooth disease type 1A: first report of a de novo duplication with a maternal origin.

Blair IP, Nash J, Gordon MJ, Nicholson GA. Blair IP, et al. Among authors: nicholson ga. Am J Hum Genet. 1996 Mar;58(3):472-6. Am J Hum Genet. 1996. PMID: 8644705 Free PMC article.

5

The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3.

Nicholson GA, Dawkins JL, Blair IP, Kennerson ML, Gordon MJ, Cherryson AK, Nash J, Bananis T. Nicholson GA, et al. Nat Genet. 1996 May;13(1):101-4. doi: 10.1038/ng0596-101. Nat Genet. 1996. PMID: 8673084

6

Fine mapping of the hereditary sensory neuropathy type I locus on chromosome 9q22.1-->q22.3: exclusion of GAS1 and XPA.

Blair IP, Dawkins JL, Nicholson GA. Blair IP, et al. Among authors: nicholson ga. Cytogenet Cell Genet. 1997;78(2):140-4. doi: 10.1159/000134649. Cytogenet Cell Genet. 1997. PMID: 9371409

7

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

8

A YAC-based transcript map of human chromosome 9q22.1-q22.3 encompassing the loci for hereditary sensory neuropathy type I and multiple self-healing squamous epithelioma.

Blair IP, Hulme D, Dawkins JL, Nicholson GA. Blair IP, et al. Among authors: nicholson ga. Genomics. 1998 Jul 15;51(2):277-81. doi: 10.1006/geno.1998.5373. Genomics. 1998. PMID: 9722951

9

Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysis.

Hulme DJ, Blair IP, Dawkins JL, Nicholson GA. Hulme DJ, et al. Among authors: nicholson ga. Hum Genet. 2000 Jun;106(6):594-6. doi: 10.1007/s004390000306. Hum Genet. 2000. PMID: 10942106

10

Variable phenotype of Alzheimer's disease with spastic paraparesis.

Smith MJ, Kwok JB, McLean CA, Kril JJ, Broe GA, Nicholson GA, Cappai R, Hallupp M, Cotton RG, Masters CL, Schofield PR, Brooks WS. Smith MJ, et al. Among authors: nicholson ga. Ann Neurol. 2001 Jan;49(1):125-9. doi: 10.1002/1531-8249(200101)49:1<125::aid-ana21>3.0.co;2-1. Ann Neurol. 2001. PMID: 11198283

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

243 results

Search Page