Brian N. Harding, MD PhD
Affiliations: | Pathology and Laboratory Medicine | University of Pennsylvania, Philadelphia, PA, United States |
Website:
http://www.med.upenn.edu/apps/faculty/index.php/g275/p8379070Google:
"Brian Harding"Bio:
http://www.nature.com/nrneurol/journal/v6/n9/authors/nrneurol.2010.118.html
http://pathologytraining.org/FellowshipPdf.aspx?inst_prg_id=460&Dir_Edition=44
Mean distance: 106866
Cross-listing: Neuropathology Tree
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Publications
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| Viaene AN, Harding BN. (2020) The Neuropathology of MIRAGE Syndrome. Journal of Neuropathology and Experimental Neurology |
| Picarsic J, Pysher T, Zhou H, et al. (2019) BRAF V600E mutation in Juvenile Xanthogranuloma family neoplasms of the central nervous system (CNS-JXG): a revised diagnostic algorithm to include pediatric Erdheim-Chester disease. Acta Neuropathologica Communications. 7: 168 |
| Smolicz I, Fairchild A, Pickles J, et al. (2019) 49 The biology of paediatric central nervous system tumours at post-mortem Archives of Disease in Childhood. 104 |
| Adle-Biassette H, Golden JA, Harding B. (2017) Developmental and perinatal brain diseases. Handbook of Clinical Neurology. 145: 51-78 |
| Barth PG, Aronica E, Fox S, et al. (2016) Deregulated expression of EZH2 in congenital brainstem disconnection. Neuropathology and Applied Neurobiology |
| Harding BN, Moccia A, Drunat S, et al. (2016) Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons. American Journal of Human Genetics |
| Rajakulendran S, Pitceathly RD, Taanman JW, et al. (2016) A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease. Plos One. 11: e0145500 |
| Skjei KL, Church EW, Harding BN, et al. (2015) Clinical and histopathological outcomes in patients with SCN1A mutations undergoing surgery for epilepsy. Journal of Neurosurgery. Pediatrics. 1-7 |
| Harding B, Vossough A, Goldberg E, et al. (2015) Pontine tegmental cap dysplasia: neuropathological confirmation of a rare clinical/radiological syndrome. Neuropathology and Applied Neurobiology |
| Jinks RN, Puffenberger EG, Baple E, et al. (2015) Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73. Brain : a Journal of Neurology. 138: 2173-90 |