Brian N. Harding, MD PhD

Pathology and Laboratory Medicine University of Pennsylvania, Philadelphia, PA, United States 
"Brian Harding"

Mean distance: 106866
Cross-listing: Neuropathology Tree

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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
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