Wood N - Search Results

1

Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological Diseases.

Poole OV, Pizzamiglio C, Murphy D, Falabella M, Macken WL, Bugiardini E, Woodward CE, Labrum R, Efthymiou S, Salpietro V, Chelban V, Kaiyrzhanov R, Maroofian R; SYNaPS Study Group; Amato AA, Gregory A, Hayflick SJ; Queen Square Genomics; Jonvik H, Wood N, Houlden H, Vandrovcova J, Hanna MG, Pittman A, Pitceathly RDS. Poole OV, et al. Among authors: wood n. Ann Neurol. 2021 Jun;89(6):1240-1247. doi: 10.1002/ana.26063. Epub 2021 Apr 1. Ann Neurol. 2021. PMID: 33704825 Free PMC article.

2

Mitochondrial disorders in neuro-ophthalmology.

Riordan-Eva P, Wood NW. Riordan-Eva P, et al. Among authors: wood nw. Curr Opin Neurol. 1996 Feb;9(1):1-4. doi: 10.1097/00019052-199602000-00002. Curr Opin Neurol. 1996. PMID: 8722656 Review.

3

Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease.

Bandmann O, Sweeney MG, Daniel SE, Marsden CD, Wood NW. Bandmann O, et al. Among authors: wood nw. J Neurol. 1997 Apr;244(4):262-5. doi: 10.1007/s004150050082. J Neurol. 1997. PMID: 9112596

4

Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion.

Hanna MG, Davis MB, Sweeney MG, Noursadeghi M, Ellis CJ, Elliot P, Wood NW, Marsden CD. Hanna MG, et al. Among authors: wood nw. Mov Disord. 1998 Mar;13(2):339-40. doi: 10.1002/mds.870130223. Mov Disord. 1998. PMID: 9539351

5

Depletion of mitochondrial DNA by ddC in untransformed human cell lines.

Nelson I, Hanna MG, Wood NW, Harding AE. Nelson I, et al. Among authors: wood nw. Somat Cell Mol Genet. 1997 Jul;23(4):287-90. doi: 10.1007/BF02674419. Somat Cell Mol Genet. 1997. PMID: 9542530

6

Dejerine-Sottas neuropathy and PMP22 point mutations: a new base pair substitution and a possible "hot spot" on Ser72.

Marques W Jr, Thomas PK, Sweeney MG, Carr L, Wood NW. Marques W Jr, et al. Among authors: wood nw. Ann Neurol. 1998 May;43(5):680-3. doi: 10.1002/ana.410430521. Ann Neurol. 1998. PMID: 9585367

7

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

Hanna MG, Nelson IP, Rahman S, Lane RJ, Land J, Heales S, Cooper MJ, Schapira AH, Morgan-Hughes JA, Wood NW. Hanna MG, et al. Among authors: wood nw. Am J Hum Genet. 1998 Jul;63(1):29-36. doi: 10.1086/301910. Am J Hum Genet. 1998. PMID: 9634511 Free PMC article.

8

Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A).

Hanna MG, Stewart J, Schapira AH, Wood NW, Morgan-Hughes JA, Murray NM. Hanna MG, et al. Among authors: wood nw. J Neurol Neurosurg Psychiatry. 1998 Aug;65(2):248-50. doi: 10.1136/jnnp.65.2.248. J Neurol Neurosurg Psychiatry. 1998. PMID: 9703181 Free PMC article.

9

Clinical and laboratory findings in referrals for mitochondrial DNA analysis.

Lamont PJ, Surtees R, Woodward CE, Leonard JV, Wood NW, Harding AE. Lamont PJ, et al. Among authors: wood nw. Arch Dis Child. 1998 Jul;79(1):22-7. doi: 10.1136/adc.79.1.22. Arch Dis Child. 1998. PMID: 9771247 Free PMC article.

10

Ion channels and neurological disease: DNA based diagnosis is now possible, and ion channels may be important in common paroxysmal disorders.

Hanna MG, Wood NW, Kullmann DM. Hanna MG, et al. Among authors: wood nw. J Neurol Neurosurg Psychiatry. 1998 Oct;65(4):427-31. doi: 10.1136/jnnp.65.4.427. J Neurol Neurosurg Psychiatry. 1998. PMID: 9771758 Free PMC article. Review. No abstract available.

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