Harding B - Search Results

1

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. Among authors: harding b. 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

2

Intravascular inflammatory myofibroblastic tumors in infancy.

Sebire NJ, Ramsay A, Sheppard M, Malone M, Harding B, Risdon RA. Sebire NJ, et al. Among authors: harding b. Pediatr Dev Pathol. 2002 Jul-Aug;5(4):400-4. doi: 10.1007/s10024-001-0198-8. Epub 2002 May 21. Pediatr Dev Pathol. 2002. PMID: 12016524

3

Diagnostic accuracy of postmortem MRI for musculoskeletal abnormalities in fetuses and children.

Arthurs OJ, Thayyil S, Addison S, Wade A, Jones R, Norman W, Scott R, Robertson NJ, Chitty LS, Taylor AM, Sebire NJ, Offiah AC; Magnetic Resonance Imaging Autopsy Study (MaRIAS) Collaborative Group. Arthurs OJ, et al. Prenat Diagn. 2014 Dec;34(13):1254-61. doi: 10.1002/pd.4460. Epub 2014 Aug 6. Prenat Diagn. 2014. PMID: 25043483 Free article. Clinical Trial.

4

Diagnostic accuracy of post-mortem MRI for thoracic abnormalities in fetuses and children.

Arthurs OJ, Thayyil S, Olsen OE, Addison S, Wade A, Jones R, Norman W, Scott RJ, Robertson NJ, Taylor AM, Chitty LS, Sebire NJ, Owens CM; Magnetic Resonance Imaging Autopsy Study (MaRIAS) Collaborative Group. Arthurs OJ, et al. Eur Radiol. 2014 Nov;24(11):2876-84. doi: 10.1007/s00330-014-3313-8. Epub 2014 Aug 31. Eur Radiol. 2014. PMID: 25173624 Free PMC article.

5

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. PLoS One. 2016 Jan 6;11(1):e0145500. doi: 10.1371/journal.pone.0145500. eCollection 2016. PLoS One. 2016. PMID: 26735972 Free PMC article.

6

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. Among authors: harding b. Acta Neuropathol. 2010 Jul;120(1):85-96. doi: 10.1007/s00401-010-0677-y. Epub 2010 Mar 30. Acta Neuropathol. 2010. PMID: 20352236

7

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. Among authors: harding b. 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

8

Is CSF cytology a useful diagnostic procedure in staging paediatric CNS tumours?

Cohen NR, Phipps K, Harding B, Jacques TS. Cohen NR, et al. Among authors: harding b. Cytopathology. 2009 Aug;20(4):256-60. doi: 10.1111/j.1365-2303.2009.00676.x. Cytopathology. 2009. PMID: 19659957

9

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. 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

10

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. Among authors: harding b. J Neurooncol. 2010 Jul;98(3):305-18. doi: 10.1007/s11060-009-0081-4. Epub 2010 Jan 6. J Neurooncol. 2010. PMID: 20052518

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