Harding BN - Search Results

1

A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease.

Rajakulendran S, Pitceathly RD, Taanman JW, Costello H, Sweeney MG, Woodward CE, Jaunmuktane Z, Holton JL, Jacques TS, Harding BN, Fratter C, Hanna MG, Rahman S. Rajakulendran S, et al. Among authors: harding bn. PLoS One. 2016 Jan 6;11(1):e0145500. doi: 10.1371/journal.pone.0145500. eCollection 2016. PLoS One. 2016. PMID: 26735972 Free PMC article.

2

Quantification of normal range of inflammatory changes in morphologically normal pediatric muscle.

Varsani H, Newton KR, Li CK, Harding B, Holton JL, Wedderburn LR. Varsani H, et al. Muscle Nerve. 2008 Feb;37(2):259-61. doi: 10.1002/mus.20898. Muscle Nerve. 2008. PMID: 17847070

3

Epigenetic genome-wide analysis identifies BEX1 as a candidate tumour suppressor gene in paediatric intracranial ependymoma.

Karakoula K, Jacques TS, Phipps KP, Harkness W, Thompson D, Harding BN, Darling JL, Warr TJ. Karakoula K, et al. Among authors: harding bn. Cancer Lett. 2014 Apr 28;346(1):34-44. doi: 10.1016/j.canlet.2013.12.005. Epub 2013 Dec 11. Cancer Lett. 2014. PMID: 24333734

4

Role of routine neuropathological examination for determining cause of death in sudden unexpected deaths in infancy (SUDI).

Pryce JW, Paine SM, Weber MA, Harding B, Jacques TS, Sebire NJ. Pryce JW, et al. J Clin Pathol. 2012 Mar;65(3):257-61. doi: 10.1136/jclinpath-2011-200264. Epub 2011 Dec 1. J Clin Pathol. 2012. PMID: 22135027

5

Deficiency of respiratory chain complex I is a common cause of Leigh disease.

Morris AA, Leonard JV, Brown GK, Bidouki SK, Bindoff LA, Woodward CE, Harding AE, Lake BD, Harding BN, Farrell MA, Bell JE, Mirakhur M, Turnbull DM. Morris AA, et al. Among authors: harding bn, harding ae. Ann Neurol. 1996 Jul;40(1):25-30. doi: 10.1002/ana.410400107. Ann Neurol. 1996. PMID: 8687187

6

Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13.

Karakoula K, Suarez-Merino B, Ward S, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Beck J, Thomas DG, Warr TJ. Karakoula K, et al. Genes Chromosomes Cancer. 2008 Nov;47(11):1005-22. doi: 10.1002/gcc.20607. Genes Chromosomes Cancer. 2008. PMID: 18663750

7

Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisation.

Ward SJ, Karakoula K, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Darling JL, Thomas DG, Warr TJ. Ward SJ, et al. J Neurooncol. 2010 Jul;98(3):305-18. doi: 10.1007/s11060-009-0081-4. Epub 2010 Jan 6. J Neurooncol. 2010. PMID: 20052518

8

Balloon cells in human cortical dysplasia and tuberous sclerosis: isolation of a pathological progenitor-like cell.

Yasin SA, Latak K, Becherini F, Ganapathi A, Miller K, Campos O, Picker SR, Bier N, Smith M, Thom M, Anderson G, Helen Cross J, Harkness W, Harding B, Jacques TS. Yasin SA, et al. Acta Neuropathol. 2010 Jul;120(1):85-96. doi: 10.1007/s00401-010-0677-y. Epub 2010 Mar 30. Acta Neuropathol. 2010. PMID: 20352236

9

The utility of brain biopsy in pediatric cryptogenic neurological disease.

Layard Horsfall H, Toescu SM, Grover PJ, Hassell J, Sayer C, Hemingway C, Harding B, Jacques TS, Aquilina K. Layard Horsfall H, et al. J Neurosurg Pediatr. 2020 Jul 3;26(4):431-438. doi: 10.3171/2020.4.PEDS19783. Print 2020 Oct 1. J Neurosurg Pediatr. 2020. PMID: 32619987

10

Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytoma.

Potter N, Karakoula A, Phipps KP, Harkness W, Hayward R, Thompson DN, Jacques TS, Harding B, Thomas DG, Palmer RW, Rees J, Darling J, Warr TJ. Potter N, et al. Neoplasia. 2008 Aug;10(8):757-72. doi: 10.1593/neo.07914. Neoplasia. 2008. PMID: 18670637 Free PMC article.

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