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/p8379070
Google:
"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

Cross-listing: Neurotree

BETA: Related publications

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
Harding BN, Moccia A, Drunat S, et al. (2016) Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons. American Journal of Human Genetics
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
Conway RL, Pressman BD, Dobyns WB, et al. (2007) Neuroimaging findings in Macrocephaly-Capillary Malformation: A longitudinal study of 17 patients American Journal of Medical Genetics, Part A. 143: 2981-3008
Lemos MC, Harding B, Shalet SM, et al. (2007) A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1. Clinical Endocrinology. 66: 709-13
Guerrini R, Mei D, Sisodiya S, et al. (2004) Germline and mosaic mutations of FLN1 in men with periventricular heterotopia Neurology. 63: 51-56
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