| 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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