Brian N. Harding, MD PhD - Publications

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

64 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Viaene AN, Harding BN. The Neuropathology of MIRAGE Syndrome. Journal of Neuropathology and Experimental Neurology. PMID 32106287 DOI: 10.1093/Jnen/Nlaa009  0.36
2019 Picarsic J, Pysher T, Zhou H, Fluchel M, Pettit T, Whitehead M, Surrey LF, Harding B, Goldstein G, Fellig Y, Weintraub M, Mobley BC, Sharples PM, Sulis ML, Diamond EL, et al. 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. PMID 31685033 DOI: 10.1186/S40478-019-0811-6  0.35
2019 Smolicz I, Fairchild A, Pickles J, Stone T, Chalker J, Zapata JG, Wilkhu L, Yasin S, Merve A, Harding B, Hargrave D, Sebire N, Jacques T. 49 The biology of paediatric central nervous system tumours at post-mortem Archives of Disease in Childhood. 104. DOI: 10.1136/Archdischild-2019-Gosh.49  0.318
2017 Adle-Biassette H, Golden JA, Harding B. Developmental and perinatal brain diseases. Handbook of Clinical Neurology. 145: 51-78. PMID 28987191 DOI: 10.1016/B978-0-12-802395-2.00006-7  0.316
2016 Barth PG, Aronica E, Fox S, Fluiter K, Weterman MA, Poretti A, Miller DC, Boltshauser E, Harding B, Santi M, Baas F. Deregulated expression of EZH2 in congenital brainstem disconnection. Neuropathology and Applied Neurobiology. PMID 27886392 DOI: 10.1111/Nan.12368  0.309
2016 Harding BN, Moccia A, Drunat S, Soukarieh O, Tubeuf H, Chitty LS, Verloes A, Gressens P, El Ghouzzi V, Joriot S, Di Cunto F, Martins A, Passemard S, Bielas SL. Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons. American Journal of Human Genetics. PMID 27453579 DOI: 10.1016/J.Ajhg.2016.07.003  0.341
2016 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. A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease. Plos One. 11: e0145500. PMID 26735972 DOI: 10.1371/Journal.Pone.0145500  0.318
2015 Skjei KL, Church EW, Harding BN, Santi M, Holland-Bouley KD, Clancy RR, Porter BE, Heuer GG, Marsh ED. Clinical and histopathological outcomes in patients with SCN1A mutations undergoing surgery for epilepsy. Journal of Neurosurgery. Pediatrics. 1-7. PMID 26339958 DOI: 10.3171/2015.5.Peds14551  0.334
2015 Harding B, Vossough A, Goldberg E, Santi M. Pontine tegmental cap dysplasia: neuropathological confirmation of a rare clinical/radiological syndrome. Neuropathology and Applied Neurobiology. PMID 26331236 DOI: 10.1111/Nan.12281  0.313
2015 Jinks RN, Puffenberger EG, Baple E, Harding B, Crino P, Fogo AB, Wenger O, Xin B, Koehler AE, McGlincy MH, Provencher MM, Smith JD, Tran L, Al Turki S, Chioza BA, et al. 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. PMID 26070982 DOI: 10.1093/Brain/Awv153  0.331
2015 Harding BN, Kariya S, Monani UR, Chung WK, Benton M, Yum SW, Tennekoon G, Finkel RS. Spectrum of neuropathophysiology in spinal muscular atrophy type I. Journal of Neuropathology and Experimental Neurology. 74: 15-24. PMID 25470343 DOI: 10.1097/Nen.0000000000000144  0.351
2014 Nabavizadeh SA, Feygin T, Harding BN, Bilaniuk LT, Zimmerman RA, Vossough A. Imaging findings of patients with metastatic neuroblastoma to the brain. Academic Radiology. 21: 329-37. PMID 24365052 DOI: 10.1016/J.Acra.2013.10.016  0.309
2012 Pryce JW, Paine SM, Weber MA, Harding B, Jacques TS, Sebire NJ. Role of routine neuropathological examination for determining cause of death in sudden unexpected deaths in infancy (SUDI). Journal of Clinical Pathology. 65: 257-61. PMID 22135027 DOI: 10.1136/Jclinpath-2011-200264  0.322
2012 Harding B. Aspects of destructive and degenerative diseases of early life Pathology. 44. DOI: 10.1016/S0031-3025(16)32626-5  0.373
2007 Conway RL, Pressman BD, Dobyns WB, Danielpour M, Lee J, Sanchez-Lara PA, Butler MG, Zackai E, Campbell L, Saitta SC, Clericuzio CL, Milunsky JM, Hoyme HE, Shieh J, Moeschler JB, ... ... Harding B, et al. Neuroimaging findings in Macrocephaly-Capillary Malformation: A longitudinal study of 17 patients American Journal of Medical Genetics, Part A. 143: 2981-3008. PMID 18000912 DOI: 10.1002/Ajmg.A.32040  0.36
2007 Lemos MC, Harding B, Shalet SM, Thakker RV. A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1. Clinical Endocrinology. 66: 709-13. PMID 17388795 DOI: 10.1111/J.1365-2265.2007.02806.X  0.31
2007 Ali A, Christie PT, Grigorieva IV, Harding B, Van Esch H, Ahmed SF, Bitner-Glindzicz M, Blind E, Bloch C, Christin P, Clayton P, Gecz J, Gilbert-Dussardier B, Guillen-Navarro E, Hackett A, et al. Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor. Human Molecular Genetics. 16: 265-75. PMID 17210674 DOI: 10.1093/Hmg/Ddl454  0.302
2006 Bradley KJ, Cavaco BM, Bowl MR, Harding B, Cranston T, Fratter C, Besser GM, Pereira MC, Davie MWJ, Dudley N, Leite V, Sadler GP, Seller A, Thakker RV. Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours. Clinical Endocrinology. 64: 299-306. PMID 16487440 DOI: 10.1111/J.1365-2265.2006.02460.X  0.316
2006 Riney CJ, Harding B, Harkness WJ, Scott RC, Cross JH. Hippocampal sclerosis in children with lesional epilepsy is influenced by age at seizure onset. Epilepsia. 47: 159-66. PMID 16417544 DOI: 10.1111/J.1528-1167.2006.00382.X  0.305
2005 Eltze CM, Chong WK, Bhate S, Harding B, Neville BG, Cross JH. Taylor-type focal cortical dysplasia in infants: some MRI lesions almost disappear with maturation of myelination. Epilepsia. 46: 1988-92. PMID 16393166 DOI: 10.1111/J.1528-1167.2005.00339.X  0.31
2005 Thom M, Martinian L, Sisodiya SM, Cross JH, Williams G, Stoeber K, Harkness W, Harding BN. Mcm2 labelling of balloon cells in focal cortical dysplasia. Neuropathology and Applied Neurobiology. 31: 580-8. PMID 16281906 DOI: 10.1111/J.1365-2990.2005.00651.X  0.345
2005 Thom M, Martinian L, Sen A, Cross JH, Harding BN, Sisodiya SM. Cortical neuronal densities and lamination in focal cortical dysplasia. Acta Neuropathologica. 110: 383-92. PMID 16151726 DOI: 10.1007/S00401-005-1062-0  0.323
2004 Guerrini R, Mei D, Sisodiya S, Sicca F, Harding B, Takahashi Y, Dorn T, Yoshida A, Campistol J, Krämer G, Moro F, Dobyns WB, Parrini E. Germline and mosaic mutations of FLN1 in men with periventricular heterotopia Neurology. 63: 51-56. PMID 15249610 DOI: 10.1212/01.Wnl.0000132818.84827.4D  0.324
2004 Sztriha L, Guerrini R, Harding B, Stewart F, Chelloug N, Johansen JG. Clinical, MRI, and pathological features of polymicrogyria in chromosome 22q11 deletion syndrome American Journal of Medical Genetics Part A. 127: 313-317. PMID 15150787 DOI: 10.1002/Ajmg.A.30014  0.341
2004 Cavaco BM, Guerra L, Bradley KJ, Carvalho D, Harding B, Oliveira A, Santos M, Sobrinho LG, Thakker RV, Leite V. Hyperparathyroidism-Jaw Tumor Syndrome in Roma Families from Portugal Is Due to a Founder Mutation of the HRPT2 Gene The Journal of Clinical Endocrinology and Metabolism. 89: 1747-1752. PMID 15070940 DOI: 10.1210/Jc.2003-031016  0.322
2004 Dale RC, Church AJ, Surtees RA, Lees AJ, Adcock JE, Harding B, Neville BG, Giovannoni G. Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunity. Brain : a Journal of Neurology. 127: 21-33. PMID 14570817 DOI: 10.1093/Brain/Awh008  0.325
2003 Pitt M, Houlden H, Jacobs J, Mok Q, Harding B, Reilly M, Surtees R. Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1. Brain : a Journal of Neurology. 126: 2682-92. PMID 14506069 DOI: 10.1093/Brain/Awg278  0.34
2003 Baxter P, Clarke A, Cross H, Harding B, Hicks E, Livingston J, Surtees R. Idiopathic catastrophic epileptic encephalopathy presenting with acute onset intractable status Seizure-European Journal of Epilepsy. 12: 379-387. PMID 12915084 DOI: 10.1016/S1059-1311(02)00340-0  0.34
2003 Thom M, Harding BN, Lin WR, Martinian L, Cross H, Sisodiya SM. Cajal-Retzius cells, inhibitory interneuronal populations and neuropeptide Y expression in focal cortical dysplasia and microdysgenesis. Acta Neuropathologica. 105: 561-9. PMID 12734663 DOI: 10.1007/S00401-003-0673-6  0.326
2003 Devlin AM, Cross JH, Harkness W, Chong WK, Harding B, Vargha-Khadem F, Neville BG. Clinical outcomes of hemispherectomy for epilepsy in childhood and adolescence. Brain : a Journal of Neurology. 126: 556-66. PMID 12566277 DOI: 10.1093/Brain/Awg052  0.31
2002 Hartley LM, Gordon I, Harkness W, Harding B, Neville BG, Cross JH. Correlation of SPECT with pathology and seizure outcome in children undergoing epilepsy surgery. Developmental Medicine and Child Neurology. 44: 676-80. PMID 12418792 DOI: 10.1017/S0012162201002742  0.306
2002 Sisodiya SM, Thom M, Lin WR, Bajaj NP, Cross JH, Harding BN. Abnormal expression of cdk5 in focal cortical dysplasia in humans. Neuroscience Letters. 328: 217-20. PMID 12147310 DOI: 10.1016/S0304-3940(02)00520-7  0.331
2002 Sebire NJ, Ramsay A, Sheppard M, Malone M, Harding B, Risdon RA. Intravascular inflammatory myofibroblastic tumors in infancy. Pediatric and Developmental Pathology. 5: 400-404. PMID 12016524 DOI: 10.1007/S10024-001-0198-8  0.304
2002 Jacobs J, Groves M, Martinez A, Harding B. Farber's disease diagnosed by nerve biopsy Neuropathology and Applied Neurobiology. 28: 170-170. DOI: 10.1046/J.1365-2990.2002.39286_57.X  0.306
2002 Rahman S, Taanman J-, Harding BN. Alpers syndrome with mitochondrial DNA depletion Neuropathology and Applied Neurobiology. 28: 160-160. DOI: 10.1046/J.1365-2990.2002.39286_32.X  0.315
2002 McLellan A, Harding B, Cross H. Familial hemi-polymicrogyria and neurofibromatosis type 1 Neuropathology and Applied Neurobiology. 28: 158-158. DOI: 10.1046/J.1365-2990.2002.39286_28.X  0.309
2002 Thom M, Sisodiya SM, Lin W-, Cross H, Harding B. Inhibitory interneurons in focal cortical dysplasia and microdysgenesis Neuropathology and Applied Neurobiology. 28: 158-158. DOI: 10.1046/J.1365-2990.2002.39286_27.X  0.349
2001 Harding B, Thom M. Bilateral hippocampal granule cell dispersion: autopsy study of 3 infants. Neuropathology and Applied Neurobiology. 27: 245-251. PMID 11489144 DOI: 10.1046/J.0305-1846.2001.00325.X  0.324
2001 Warr T, Ward S, Burrows J, Harding B, Wilkins P, Harkness W, Hayward R, Darling J, Thomas D. Identification of extensive genomic loss and gain by comparative genomic hybridisation in malignant astrocytoma in children and young adults. Genes, Chromosomes & Cancer. 31: 15-22. PMID 11284031 DOI: 10.1002/Gcc.1113  0.307
2000 Dale RC, de Sousa C, Chong WK, Cox TC, Harding B, Neville BG. Acute disseminated encephalomyelitis, multiphasic disseminated encephalomyelitis and multiple sclerosis in children. Brain : a Journal of Neurology. 123: 2407-22. PMID 11099444 DOI: 10.1093/Brain/123.12.2407  0.307
1999 Copp AJ, Harding BN. Neuronal migration disorders in humans and in mouse models--an overview. Epilepsy Research. 36: 133-41. PMID 10515161 DOI: 10.1016/S0920-1211(99)00047-9  0.334
1998 Bailey A, Luthert P, Dean A, Harding B, Janota I, Montgomery M, Rutter M, Lantos P. A clinicopathological study of autism. Brain. 121: 889-905. PMID 9619192 DOI: 10.1093/Brain/121.5.889  0.333
1997 Martland T, Harding BN, Morton RE, Young I. Dentato-olivary dysplasia in sibs: an autosomal recessive disorder? Journal of Medical Genetics. 34: 1021-3. PMID 9429148 DOI: 10.1136/Jmg.34.12.1021  0.353
1997 Ross ME, Allen KM, Srivastava AK, Featherstone T, Gleeson JG, Hirsch B, Harding BN, Andermann E, Abdullah R, Berg M, Czapansky-Bielman D, Flanders DJ, Guerrini R, Motté J, Mira AP, et al. Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain. Human Molecular Genetics. 6: 555-62. PMID 9097958 DOI: 10.1093/Hmg/6.4.555  0.313
1996 Reardon W, Harding B, Winter RM, Baraitser M. Hemihypertrophy, hemimegalencephaly, and polydactyly American Journal of Medical Genetics. 66: 144-149. PMID 8958320 DOI: 10.1002/(Sici)1096-8628(19961211)66:2<144::Aid-Ajmg4>3.0.Co;2-R  0.319
1996 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. Deficiency of respiratory chain complex I is a common cause of Leigh disease. Annals of Neurology. 40: 25-30. PMID 8687187 DOI: 10.1002/Ana.410400107  0.306
1995 Harding BN, Alsanjari N, Smith SJ, Wiles CM, Thrush D, Miller DH, Scaravilli F, Harding AE. Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adults. Journal of Neurology, Neurosurgery, and Psychiatry. 58: 320-5. PMID 7897414 DOI: 10.1136/Jnnp.58.3.320  0.357
1995 Harding B, Ellis D, Malcolm S. A case of Pelizaeus-Merzbacher disease showing increased dosage of the proteolipid protein gene. Neuropathology and Applied Neurobiology. 21: 111-115. PMID 7541900 DOI: 10.1111/J.1365-2990.1995.Tb01036.X  0.323
1994 Raymond AA, Halpin SF, Alsanjari N, Cook MJ, Kitchen ND, Fish DR, Stevens JM, Harding BN, Scaravilli F, Kendall B. Dysembryoplastic neuroepithelial tumor. Features in 16 patients. Brain : a Journal of Neurology. 117: 461-75. PMID 8032857 DOI: 10.1093/Brain/117.3.461  0.339
1994 Cavanagh JB, Harding BN. Pathogenic factors underlying the lesions in Leigh's disease. Tissue responses to cellular energy deprivation and their clinico-pathological consequences. Brain : a Journal of Neurology. 117: 1357-76. PMID 7820572 DOI: 10.1093/Brain/117.6.1357  0.343
1993 Pridmore CL, Baraitser M, Harding B, Boyd SG, Kendall B, Brett EM. Alexander's disease: clues to diagnosis. Journal of Child Neurology. 8: 134-144. PMID 8505475 DOI: 10.1177/088307389300800205  0.34
1992 Mcshane MA, Boyd S, Harding B, Brett EM, Wilson J. Progressive bulbar paralysis of childhood. A reappraisal of Fazio-Londe disease. Brain. 115: 1889-1900. PMID 1486466 DOI: 10.1093/Brain/115.6.1889  0.352
1991 Horslen SP, Clayton PT, Harding BN, Hall NA, Keir G, Winchester B. Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome. Archives of Disease in Childhood. 66: 1027-32. PMID 1929507 DOI: 10.1136/Adc.66.9.1027  0.334
1991 Scheffer IE, Baraitser M, Wilson J, Harding B, Kendall B, Brett EM. Pelizaeus-Merzbacher disease: classical or connatal? Neuropediatrics. 22: 71-78. PMID 1857497 DOI: 10.1055/S-2008-1071420  0.348
1991 Harding BN, Leonard JV, Erdohazi M. Propionic acidaemia: a neuropathological study of two patients presenting in infancy. Neuropathology and Applied Neurobiology. 17: 133-8. PMID 1857488 DOI: 10.1111/J.1365-2990.1991.Tb00704.X  0.313
1991 Harding BN, Boyd SG. Intractable seizures from infancy can be associated with dentato-olivary dysplasia. Journal of the Neurological Sciences. 104: 157-65. PMID 1719137 DOI: 10.1016/0022-510X(91)90305-Q  0.338
1990 Harding BN. Progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome): a personal review. Journal of Child Neurology. 5: 273-87. PMID 2246481 DOI: 10.1177/088307389000500402  0.31
1989 Patton MA, Giannelli F, Francis AJ, Baraitser M, Harding B, Williams AJ. Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studies. Journal of Medical Genetics. 26: 154-9. PMID 2468771 DOI: 10.1136/Jmg.26.3.154  0.316
1988 Harding BN, Dunger DB, Grant DB, Erdohazi M. Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities. Journal of Neurology, Neurosurgery, and Psychiatry. 51: 385-90. PMID 3162953 DOI: 10.1136/Jnnp.51.3.385  0.334
1987 Ramaekers VT, Lake BD, Harding B, Boyd S, Harden A, Brett EM, Wilson J. Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight cases. Neuropediatrics. 18: 170-5. PMID 3683759 DOI: 10.1055/S-2008-1052474  0.335
1987 Kendall BE, Boyd SG, Egger J, Harding BN. Progressive neuronal degeneration of childhood with liver disease. Computed tomographic features. Neuroradiology. 29: 174-80. PMID 3587592 DOI: 10.1007/Bf00327545  0.347
1987 Egger J, Harding BN, Boyd SG, Wilson J, Erdohazi M. Progressive neuronal degeneration of childhood (PNDC) with liver disease. Clinical Pediatrics. 26: 167-73. PMID 2435443 DOI: 10.1177/000992288702600401  0.351
1985 Torres LF, Grant N, Harding BN, Scaravilli F. Intracerebral neuroblastoma. Report of a case with neuronal maturation and long survival. Acta Neuropathologica. 68: 110-4. PMID 4072619 DOI: 10.1007/Bf00688631  0.311
1985 Harding BN, Tudway AJ, Wilson J. Neuropathological studies in a child showing some features of the Rett syndrome. Brain & Development. 7: 342-4. PMID 4061769 DOI: 10.1016/S0387-7604(85)80041-3  0.317
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