| 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 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2014 |
Roth JJ, Santi M, Rorke-Adams LB, Harding BN, Busse TM, Tooke LS, Biegel JA. Diagnostic application of high resolution single nucleotide polymorphism array analysis for children with brain tumors. Cancer Genetics. 207: 111-23. PMID 24767714 DOI: 10.1016/J.Cancergen.2014.03.002 |
0.3 |
|
| 2015 |
Roth JJ, Santi M, Pollock AN, Harding BN, Rorke-Adams LB, Tooke LS, Biegel JA. Chromosome band 7q34 deletions resulting in KIAA1549-BRAF and FAM131B-BRAF fusions in pediatric low-grade Gliomas. Brain Pathology (Zurich, Switzerland). 25: 182-92. PMID 25040262 DOI: 10.1111/Bpa.12167 |
0.299 |
|
| 2010 |
Golden JA, Harding BN. Cortical malformations: unfolding polymicrogyria. Nature Reviews. Neurology. 6: 471-2. PMID 20811463 DOI: 10.1038/Nrneurol.2010.118 |
0.299 |
|
| 2001 |
Ward S, Harding B, Wilkins P, Harkness W, Hayward R, Darling JL, Thomas DG, Warr T. Gain of 1q and loss of 22 are the most common changes detected by comparative genomic hybridisation in paediatric ependymoma. Genes, Chromosomes & Cancer. 32: 59-66. PMID 11477662 DOI: 10.1002/Gcc.1167 |
0.297 |
|
| 1991 |
Wroe SJ, Pires M, Harding B, Youl BD, Shorvon S. Whipple's disease confined to the CNS presenting with multiple intracerebral mass lesions. Journal of Neurology, Neurosurgery, and Psychiatry. 54: 989-992. PMID 1724783 DOI: 10.1136/Jnnp.54.11.989 |
0.296 |
|
| 2004 |
Ansorge O, Giunti P, Michalik A, Van Broeckhoven C, Harding B, Wood N, Scaravilli F. Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats. Annals of Neurology. 56: 448-52. PMID 15349877 DOI: 10.1002/Ana.20230 |
0.295 |
|
| 2010 |
Yasin SA, Latak K, Becherini F, Ganapathi A, Miller K, Campos O, Picker SR, Bier N, Smith M, Thom M, Anderson G, Helen Cross J, Harkness W, Harding B, Jacques TS. Balloon cells in human cortical dysplasia and tuberous sclerosis: isolation of a pathological progenitor-like cell. Acta Neuropathologica. 120: 85-96. PMID 20352236 DOI: 10.1007/S00401-010-0677-Y |
0.294 |
|
| 2002 |
Turner JJO, Leotlela PD, Pannett AAJ, Forbes SA, Bassett JHD, Harding B, Christie PT, Bowen-Jones D, Ellard S, Hattersley A, Jackson CE, Pope R, Quarrell OW, Trembath R, Thakker RV. Frequent Occurrence of an Intron 4 Mutation in Multiple Endocrine Neoplasia Type 1 The Journal of Clinical Endocrinology and Metabolism. 87: 2688-2693. DOI: 10.1210/Jc.87.6.2688 |
0.293 |
|
| 2001 |
Eriksson SH, Thom M, Heffernan J, Lin WR, Harding BN, Squier MV, Sisodiya SM. Persistent reelin-expressing Cajal-Retzius cells in polymicrogyria. Brain : a Journal of Neurology. 124: 1350-61. PMID 11408330 DOI: 10.1093/Brain/124.7.1350 |
0.293 |
|
| 2004 |
Chung BHY, Ip PPK, Wong VCN, Lo JYC, Harding B. Acute fulminant subacute sclerosing panencephalitis with absent measles and PCR studies in cerebrospinal fluid Pediatric Neurology. 31: 222-224. PMID 15351025 DOI: 10.1016/J.Pediatrneurol.2004.03.016 |
0.292 |
|
| 2002 |
Cross J, Hartley L, Harkness W, Harding B, Neville B, Gordon I. Correlation of single photon emission computed tomography with pathology and seizure outcome in children undergoing epilepsy surgery Neuropathology and Applied Neurobiology. 28: 159-160. DOI: 10.1046/J.1365-2990.2002.39286_31.X |
0.291 |
|
| 2004 |
Andrew Nesbit M, Bowl MR, Harding B, Schlessinger D, Whyte MP, Thakker RV. X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase. Genomics. 84: 1060-70. PMID 15533723 DOI: 10.1016/J.Ygeno.2004.08.003 |
0.291 |
|
| 1991 |
Woody RC, Harding BN, Brumback RA, Leech RW. Absence of beta-amyloid immunoreactivity in mesial temporal lobe in Cockayne's syndrome. Journal of Child Neurology. 6: 32-4. PMID 1825835 DOI: 10.1177/088307389100600106 |
0.289 |
|
| 2004 |
Nesbit MA, Bowl MR, Harding B, Ali A, Ayala A, Crowe C, Dobbie A, Hampson G, Holdaway I, Levine MA, McWilliams R, Rigden S, Sampson J, Williams AJ, Thakker RV. Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome. The Journal of Biological Chemistry. 279: 22624-34. PMID 14985365 DOI: 10.1074/Jbc.M401797200 |
0.289 |
|
| 2007 |
Thom M, Martinian L, Sen A, Squier W, Harding BN, Cross JH, Harkness W, McEvoy A, Sisodiya SM. An investigation of the expression of G1-phase cell cycle proteins in focal cortical dysplasia type IIB. Journal of Neuropathology and Experimental Neurology. 66: 1045-55. PMID 17984686 DOI: 10.1097/Nen.0B013E3181598D23 |
0.288 |
|
| 2002 |
Sisodiya SM, Lint WR, Harding BN, Squier MV, Thom M. Drug resistance in epilepsy: human epilepsy. Novartis Foundation Symposium. 243: 167-74; discussion 1. PMID 11990775 DOI: 10.1002/0470846356.Ch12 |
0.286 |
|
| 2010 |
Ward SJ, Karakoula K, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Darling JL, Thomas DG, Warr TJ. Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisation. Journal of Neuro-Oncology. 98: 305-18. PMID 20052518 DOI: 10.1007/S11060-009-0081-4 |
0.286 |
|
| 1985 |
Winter RM, Wigglesworth J, Harding BN. Osteodysplastic primordial dwarfism: report of a further patient with manifestations similar to those seen in patients with types I and III. American Journal of Medical Genetics. 21: 569-74. PMID 4025388 DOI: 10.1002/Ajmg.1320210318 |
0.286 |
|
| 1988 |
Harding B, Baumer JA. Congenital varicella-zoster. A serologically proven case with necrotizing encephalitis and malformation. Acta Neuropathologica. 76: 311-315. PMID 2850700 DOI: 10.1007/Bf00687781 |
0.286 |
|
| 2007 |
Sen A, Thom M, Martinian L, Harding B, Cross JH, Nikolic M, Sisodiya SM. Pathological Tau Tangles Localize to Focal Cortical Dysplasia in Older Patients Epilepsia. 48: 1447-1454. PMID 17441989 DOI: 10.1111/J.1528-1167.2007.01107.X |
0.284 |
|
| 2002 |
Sisodiya SM, Lin WR, Harding BN, Squier MV, Thom M. Drug resistance in epilepsy: expression of drug resistance proteins in common causes of refractory epilepsy. Brain : a Journal of Neurology. 125: 22-31. PMID 11834590 DOI: 10.1093/Brain/Awf002 |
0.283 |
|
| 2005 |
Gunny RS, Hayward RD, Phipps KP, Harding BN, Saunders DE. Spontaneous regression of residual low-grade cerebellar pilocytic astrocytomas in children. Pediatric Radiology. 35: 1086-91. PMID 16047140 DOI: 10.1007/S00247-005-1546-Z |
0.283 |
|
| 2001 |
Costa C, Harding B, Copp AJ. Neuronal migration defects in the Dreher (Lmx1a) mutant mouse: role of disorders of the glial limiting membrane. Cerebral Cortex (New York, N.Y. : 1991). 11: 498-505. PMID 11375911 DOI: 10.1093/Cercor/11.6.498 |
0.282 |
|
| 1997 |
Stapleton SR, David KM, Harkness WF, Harding BN. Central neurocytoma of the cervical spinal cord. Journal of Neurology, Neurosurgery, and Psychiatry. 63: 119. PMID 9221982 DOI: 10.1136/Jnnp.63.1.119 |
0.281 |
|
| 1992 |
Bhattacharjee MB, Wroe SJ, Harding BN, Powell M. Sinus histiocytosis with massive lymphadenopathy--isolated suprasellar involvement. Journal of Neurology, Neurosurgery, and Psychiatry. 55: 156-8. PMID 1538225 DOI: 10.1136/Jnnp.55.2.156 |
0.28 |
|
| 2020 |
Layard Horsfall H, Toescu SM, Grover PJ, Hassell J, Sayer C, Hemingway C, Harding B, Jacques TS, Aquilina K. The utility of brain biopsy in pediatric cryptogenic neurological disease. Journal of Neurosurgery. Pediatrics. 1-8. PMID 32619987 DOI: 10.3171/2020.4.Peds19783 |
0.279 |
|
| 1990 |
Jacobs JM, Harding BN, Lake BD, Payan J, Wilson J. Peripheral neuropathy in Leigh's disease. Brain : a Journal of Neurology. 113: 447-62. PMID 2158380 DOI: 10.1093/Brain/113.2.447 |
0.278 |
|
| 2018 |
López GY, Perry A, Harding B, Li M, Santi M. CDKN2A/B Loss is Associated with Anaplastic Transformation in a Case of NTRK2 Fusion-positive Pilocytic Astrocytoma. Neuropathology and Applied Neurobiology. PMID 29804288 DOI: 10.1111/Nan.12503 |
0.278 |
|
| 2003 |
Sisodiya SM, Martinian L, Scheffer GL, van der Valk P, Cross JH, Scheper RJ, Harding BN, Thom M. Major vault protein, a marker of drug resistance, is upregulated in refractory epilepsy. Epilepsia. 44: 1388-96. PMID 14636345 DOI: 10.1046/J.1528-1157.2003.21803.X |
0.278 |
|
| 2005 |
McLellan A, Davies S, Heyman I, Harding B, Harkness W, Taylor D, Neville BGR, Cross JH. Psychopathology in children with epilepsy before and after temporal lobe resection Developmental Medicine & Child Neurology. 47: 666-672. PMID 16174309 DOI: 10.1017/S0012162205001362 |
0.278 |
|
| 2005 |
Lemos MC, Kotanko P, Christie PT, Harding B, Javor T, Smith C, Eastell R, Thakker RV. A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosis. The Journal of Clinical Endocrinology and Metabolism. 90: 5386-5392. PMID 15985493 DOI: 10.1210/Jc.2004-2520 |
0.277 |
|
| 2005 |
Bowl MR, Nesbit MA, Harding B, Levy E, Jefferson A, Volpi E, Rizzoti K, Lovell-Badge R, Schlessinger D, Whyte MP, Thakker RV. An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism. The Journal of Clinical Investigation. 115: 2822-31. PMID 16167084 DOI: 10.1172/Jci24156 |
0.277 |
|
| 2001 |
Salvatori R, Thakker RV, Lopes MB, Fan X, Eswara JR, Ellison D, Lees P, Harding B, Yang I, Levine MA. Absence of mutations in the growth hormone (GH)-releasing hormone receptor gene in GH-secreting pituitary adenomas. Clinical Endocrinology. 54: 301-7. PMID 11298081 DOI: 10.1046/J.1365-2265.2001.01213.X |
0.277 |
|
| 1990 |
Bentley AJ, Parkinson MC, Harding BN, Bains RM, Lantos PL. A comparative morphological and immunohistochemical study of testicular seminomas and intracranial germinomas. Histopathology. 17: 443-9. PMID 2076869 DOI: 10.1111/J.1365-2559.1990.Tb00766.X |
0.277 |
|
| 2008 |
Karakoula K, Suarez-Merino B, Ward S, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Beck J, Thomas DG, Warr TJ. Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13. Genes, Chromosomes & Cancer. 47: 1005-22. PMID 18663750 DOI: 10.1002/Gcc.20607 |
0.276 |
|
| 2002 |
Turner JJO, Leotlela PD, Pannett AAJ, Harding B, Thakker RV. Frequent Occurrence of An Intron 4 Mutation in Multiple Endocrine Neoplasia Type 1 (Men1) Clinical Science. 103. DOI: 10.1042/Cs103020Pa |
0.276 |
|
| 2009 |
Lemos MC, Harding B, Reed AA, Jeyabalan J, Walls GV, Bowl MR, Sharpe J, Wedden S, Moss JE, Ross A, Davidson D, Thakker RV. Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiers. The Journal of Endocrinology. 203: 133-42. PMID 19587266 DOI: 10.1677/Joe-09-0124 |
0.274 |
|
| 1986 |
Harding BN, Egger J, Portmann B, Erdohazi M. Progressive neuronal degeneration of childhood with liver disease. A pathological study. Brain : a Journal of Neurology. 109: 181-206. PMID 3942854 DOI: 10.1093/Brain/109.1.181 |
0.274 |
|
| 2002 |
Barnes NP, Pollock JR, Harding B, Hayward RD. Papillary glioneuronal tumour in a 4-year-old Pediatric Neurosurgery. 36: 266-270. PMID 12053046 DOI: 10.1159/000058431 |
0.274 |
|
| 2008 |
Potter N, Karakoula A, Phipps KP, Harkness W, Hayward R, Thompson DN, Jacques TS, Harding B, Thomas DG, Palmer RW, Rees J, Darling J, Warr TJ. Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytoma. Neoplasia (New York, N.Y.). 10: 757-72. PMID 18670637 DOI: 10.1593/Neo.07914 |
0.274 |
|
| 1998 |
Harding BN, Win N, Scott R, Cross H. BOTH HIPPOCAMPAL SCLEROSIS AND FASCIA DENTATA DISORGANISATION MAKE IMPORTANT CONTRIBUTIONS TO TEMPORAL LOBE PATHOLOGY IN CHILDHOOD EPILEPSY Journal of Neuropathology and Experimental Neurology. 57: 514. DOI: 10.1097/00005072-199805000-00198 |
0.271 |
|
| 2012 |
Harding B. Mitochondrial diseases of the CNS Pathology. 44. DOI: 10.1016/S0031-3025(16)32624-1 |
0.269 |
|
| 2017 |
Walls GV, Stevenson M, Lines KE, Newey PJ, Reed AA, Bowl MR, Jeyabalan J, Harding B, Bradley KJ, Manek S, Chen J, Wang P, Williams BO, Teh BT, Thakker RV. Mice deleted for cell division cycle 73 gene develop parathyroid and uterine tumours: model for the hyperparathyroidism-jaw tumour syndrome. Oncogene. PMID 28288139 DOI: 10.1038/Onc.2017.43 |
0.268 |
|
| 1989 |
Winter RM, Harding BN, Hyde J. Unknown syndrome: pachygyria, joint contractures, and facial abnormalities. Journal of Medical Genetics. 26: 788-9. PMID 2614803 DOI: 10.1136/Jmg.26.12.788 |
0.268 |
|
| 2013 |
Gorvin CM, Wilmer MJ, Piret SE, Harding B, van den Heuvel LP, Wrong O, Jat PS, Lippiat JD, Levtchenko EN, Thakker RV. Receptor-mediated endocytosis and endosomal acidification is impaired in proximal tubule epithelial cells of Dent disease patients. Proceedings of the National Academy of Sciences of the United States of America. 110: 7014-9. PMID 23572577 DOI: 10.1073/Pnas.1302063110 |
0.268 |
|
| 2016 |
Gmuca S, Boos MD, Treece A, Narula S, Billinghurst L, Bhatti T, Laje P, Perman MJ, Vossough A, Harding B, Burnham J, Banwell B. Degos disease mimicking primary vasculitis of the CNS. Neurology® Neuroimmunology & Neuroinflammation. 3: e206. PMID 26894208 DOI: 10.1212/Nxi.0000000000000206 |
0.265 |
|
| 2000 |
McEvoy AW, Harding BN, Phipps KP, Ellison DW, Elsmore AJ, Thompson D, Harkness W, Hayward RD. Management of choroid plexus tumours in children: 20 years experience at a single neurosurgical centre. Pediatric Neurosurgery. 32: 192-9. PMID 10940770 DOI: 10.1159/000028933 |
0.265 |
|
| 2005 |
Kennedy AM, Inada M, Krane SM, Christie PT, Harding B, López-OtÃn C, Sánchez LM, Pannett AA, Dearlove A, Hartley C, Byrne MH, Reed AA, Nesbit MA, Whyte MP, Thakker RV. MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO). The Journal of Clinical Investigation. 115: 2832-42. PMID 16167086 DOI: 10.1172/Jci22900 |
0.265 |
|
| 2009 |
Cohen NR, Phipps K, Harding B, Jacques TS. Is CSF cytology a useful diagnostic procedure in staging paediatric CNS tumours? Cytopathology : Official Journal of the British Society For Clinical Cytology. 20: 256-60. PMID 19659957 DOI: 10.1111/J.1365-2303.2009.00676.X |
0.263 |
|
| 1986 |
Thompson EM, Harding BN, Lake BD, Smith SC. Necropsy findings in a child with FG syndrome. Journal of Medical Genetics. 23: 372-3. PMID 3746847 DOI: 10.1136/Jmg.23.4.372 |
0.263 |
|
| 2003 |
Stacey JM, Turner JJ, Harding B, Nesbit MA, Kotanko P, Lhotta K, Puig JG, Torres RJ, Thakker RV. Genetic mapping studies of familial juvenile hyperuricemic nephropathy on chromosome 16p11-p13. The Journal of Clinical Endocrinology and Metabolism. 88: 464-70. PMID 12519891 DOI: 10.1210/Jc.2002-021268 |
0.262 |
|
| 2014 |
Karakoula K, Jacques TS, Phipps KP, Harkness W, Thompson D, Harding BN, Darling JL, Warr TJ. Epigenetic genome-wide analysis identifies BEX1 as a candidate tumour suppressor gene in paediatric intracranial ependymoma. Cancer Letters. 346: 34-44. PMID 24333734 DOI: 10.1016/J.Canlet.2013.12.005 |
0.262 |
|
| 2012 |
Hannan FM, Nesbit MA, Zhang C, Cranston T, Curley AJ, Harding B, Fratter C, Rust N, Christie PT, Turner JJ, Lemos MC, Bowl MR, Bouillon R, Brain C, Bridges N, et al. Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites. Human Molecular Genetics. 21: 2768-78. PMID 22422767 DOI: 10.1093/Hmg/Dds105 |
0.261 |
|
| 2000 |
Lewandowicz GM, Harding B, Harkness W, Hayward R, Thomas DG, Darling JL. Chemosensitivity in childhood brain tumours in vitro: evidence of differential sensitivity to lomustine (CCNU) and vincristine. European Journal of Cancer (Oxford, England : 1990). 36: 1955-64. PMID 11000577 DOI: 10.1016/S0959-8049(00)00245-8 |
0.261 |
|
| 2018 |
Arellano JI, Harding B, Thomas JL. Adult Human Hippocampus: No New Neurons in Sight. Cerebral Cortex (New York, N.Y. : 1991). PMID 29746611 DOI: 10.1093/Cercor/Bhy106 |
0.259 |
|
| 1986 |
Clayton PT, Smith I, Harding B, Hyland K, Leonard JV, Leeming RJ. Subacute combined degeneration of the cord, dementia and parkinsonism due to an inborn error of folate metabolism. Journal of Neurology, Neurosurgery, and Psychiatry. 49: 920-7. PMID 3755752 DOI: 10.1136/Jnnp.49.8.920 |
0.258 |
|
| 2006 |
Sisodiya SM, Martinian L, Scheffer GL, van der Valk P, Scheper RJ, Harding BN, Thom M. Vascular colocalization of P-glycoprotein, multidrug-resistance associated protein 1, breast cancer resistance protein and major vault protein in human epileptogenic pathologies. Neuropathology and Applied Neurobiology. 32: 51-63. PMID 16409553 DOI: 10.1111/J.1365-2990.2005.00699.X |
0.256 |
|
| 1981 |
Harding B, Erdohazi M. Traumatic transection of the brainstem Journal of Neurology, Neurosurgery, and Psychiatry. 44: 1156-1158. PMID 7334413 DOI: 10.1136/Jnnp.44.12.1156 |
0.255 |
|
| 2009 |
Harding B, Lemos MC, Reed AA, Walls GV, Jeyabalan J, Bowl MR, Tateossian H, Sullivan N, Hough T, Fraser WD, Ansorge O, Cheeseman MT, Thakker RV. Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia. Endocrine-Related Cancer. 16: 1313-27. PMID 19620250 DOI: 10.1677/Erc-09-0082 |
0.251 |
|
| 2018 |
Patel P, Ross A, Henretig FM, Liu G, Harding B, Panzer J. Clinical Reasoning: A 12-year-old girl with headache and change in mental status. Neurology. 90: 524-529. PMID 29530960 DOI: 10.1212/Wnl.0000000000005116 |
0.251 |
|
| 2004 |
Harding B, Risdon RA, Krous HF. Shaken baby syndrome Bmj. 328: 720-721. PMID 15044268 DOI: 10.1136/Bmj.328.7442.720 |
0.248 |
|
| 2018 |
Jain P, Surrey LF, Straka J, Luo M, Lin F, Harding B, Resnick AC, Storm PB, Buccoliero AM, Santi M, Li MM, Waanders AJ. Novel FGFR2-INA fusion identified in two low-grade mixed neuronal-glial tumors drives oncogenesis via MAPK and PI3K/mTOR pathway activation. Acta Neuropathologica. PMID 29767381 DOI: 10.1007/S00401-018-1864-5 |
0.246 |
|
| 2012 |
Walls GV, Lemos MC, Javid M, Bazan-Peregrino M, Jeyabalan J, Reed AA, Harding B, Tyler DJ, Stuckey DJ, Piret S, Christie PT, Ansorge O, Clarke K, Seymour L, Thakker RV. MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary adenomas. Cancer Research. 72: 5060-8. PMID 22915754 DOI: 10.1158/0008-5472.Can-12-1821 |
0.246 |
|
| 2012 |
Walls GV, Reed AA, Jeyabalan J, Javid M, Hill NR, Harding B, Thakker RV. Proliferation rates of multiple endocrine neoplasia type 1 (MEN1)-associated tumors. Endocrinology. 153: 5167-79. PMID 23024266 DOI: 10.1210/En.2012-1675 |
0.246 |
|
| 2009 |
Potter NE, Phipps K, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Thomas DG, Rees J, Darling JL, Warr TJ. Astrocytoma derived short-term cell cultures retain molecular signatures characteristic of the tumour in situ. Experimental Cell Research. 315: 2835-46. PMID 19523942 DOI: 10.1016/J.Yexcr.2009.06.003 |
0.243 |
|
| 2008 |
Varsani H, Newton KR, Li CK, Harding B, Holton JL, Wedderburn LR. Quantification of normal range of inflammatory changes in morphologically normal pediatric muscle. Muscle & Nerve. 37: 259-61. PMID 17847070 DOI: 10.1002/Mus.20898 |
0.241 |
|
| 2007 |
Wedderburn LR, Varsani H, Li CK, Newton KR, Amato AA, Banwell B, Bove KE, Corse AM, Emslie-Smith A, Harding B, Hoogendijk J, Lundberg IE, Marie S, Minetti C, Nennesmo I, et al. International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trials. Arthritis and Rheumatism. 57: 1192-201. PMID 17907237 DOI: 10.1002/Art.23012 |
0.24 |
|
| 1984 |
Krarup C, Davis CH, Symon L, Harding BN, Hay RJ. Spinal blastomycosis--case report. Journal of Neurology, Neurosurgery, and Psychiatry. 47: 217-8. PMID 6707665 DOI: 10.1136/Jnnp.47.2.217 |
0.236 |
|
| 1973 |
Harding BN. An ultrastructural study of the centre median and ventrolateral thalamic nuclei of the monkey. Brain Research. 54: 335-40. PMID 4196751 DOI: 10.1016/0006-8993(73)90057-7 |
0.235 |
|
| 2008 |
Jacques TS, Miller K, Rampling D, Gatscher S, Harding B. Peritoneal dissemination of a malignant glioma. Cytopathology : Official Journal of the British Society For Clinical Cytology. 19: 264-6. PMID 18093223 DOI: 10.1111/J.1365-2303.2007.00510.X |
0.23 |
|
| 2005 |
Hall NJ, Smith VV, Harding B, Pierro A, Eaton S. Intestinal ischemia-reperfusion injury does not lead to acute central nervous system damage. The Journal of Surgical Research. 129: 288-91. PMID 15936774 DOI: 10.1016/J.Jss.2005.04.036 |
0.23 |
|
| 2002 |
Rahman S, J-W T, Harding B, Aam M. Alpers Syndrome with Mitochondrial Dna Depletion Clinical Science. 103. DOI: 10.1042/Cs103051P |
0.228 |
|
| 1973 |
Harding BN. An ultrastructural study of the termination of afferent fibres within the ventrolateral and centre median nuclei of the monkey thalamus. Brain Research. 54: 341-6. PMID 4196752 DOI: 10.1016/0006-8993(73)90058-9 |
0.225 |
|
| 1977 |
Harding BN, Powell TP. An electron microscopic study of the centre-median and ventrolateral nuclei of the thalamus in the monkey. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 279: 357-412. PMID 19794 DOI: 10.1098/Rstb.1977.0094 |
0.224 |
|
| 2013 |
Prashad PS, Marcus CL, Brown LW, Dlugos DJ, Feygin T, Harding BN, Heuer GG, Mason TB. Brain tumor presenting as somnambulism in an adolescent. Pediatric Neurology. 49: 209-12. PMID 23835274 DOI: 10.1016/J.Pediatrneurol.2013.04.022 |
0.224 |
|
| 2021 |
Burke EA, Sturgeon M, Zastrow DB, Fernandez L, Prybol C, Marwaha S, Frothingham EP, Ward PA, Eng CM, Fresard L, Montgomery SB, Enns GM, Fisher PG, Wolfe LA, Harding B, et al. Compound heterozygous variants in progressive myoclonus epilepsy. Journal of Neurogenetics. 1-10. PMID 33970744 DOI: 10.1080/01677063.2021.1892095 |
0.222 |
|
| 1999 |
Harding BN, Thom M. Bilateral granule cell dispersion in the hippocampi of 3 infants at autopsy. Journal of Neuropathology and Experimental Neurology. 58: 519. DOI: 10.1097/00005072-199905000-00051 |
0.222 |
|
| 2002 |
Turner JJO, Stacey JM, Harding B, Nesbit MA, Kotanko P, Lhotta K, Puig JG, Torres RJ, Thakker RV. Mapping of Familial Juvenile Hyperuricaemic Nephropathy on Chromosome 16P12 in Six Families Clinical Science. 103. DOI: 10.1042/Cs103024Pa |
0.219 |
|
| 2008 |
Harding B. Alexander's Disease Developmental Medicine & Child Neurology. 35: 1025-1025. PMID 8224558 DOI: 10.1111/J.1469-8749.1993.Tb11588.X |
0.218 |
|
| 1986 |
Leonard JV, Pembrey ME, Oley CA, Harding BN. Neuropathologic changes in ornithine carbamoyl transferase deficiency. The Journal of Pediatrics. 109: 1074. PMID 3783335 DOI: 10.1016/S0022-3476(86)80304-3 |
0.209 |
|
| 2019 |
Jain P, Surrey LF, Zhang B, Straka J, Zhao X, Storm PB, Resnick AC, Harding BN, Li MM, Buccoliero AM, Santi M, Waanders AJ. Lgg-14. The Genetic Landscape Of Dysembryoplastic Neuroepithelial Tumors Neuro-Oncology. 21. DOI: 10.1093/Neuonc/Noz036.157 |
0.207 |
|
| 1996 |
Harding B. Laminar Heterotopia: A Possible Failure Of Programmed Cell Death? Journal of Neuropathology and Experimental Neurology. 55: 610. DOI: 10.1097/00005072-199605000-00035 |
0.206 |
|
| 2006 |
Harding B, Curley AJ, Hannan FM, Christie PT, Bowl MR, Turner JJ, Barber M, Gillham-Nasenya I, Hampson G, Spector TD, Thakker RV. Functional characterization of calcium sensing receptor polymorphisms and absence of association with indices of calcium homeostasis and bone mineral density. Clinical Endocrinology. 65: 598-605. PMID 17054460 DOI: 10.1111/J.1365-2265.2006.02634.X |
0.206 |
|
| 1990 |
Harding BN. Rosenthal fibers in Alexander's disease. Journal of Child Neurology. 5: 259-60. PMID 2398242 DOI: 10.1177/088307389000500323 |
0.2 |
|
| 1971 |
Harding BN. Dendro-dendritic synapses, including reciprocal synapses, in the ventrolateral nucleus of the monkey thalamus. Brain Research. 34: 181-5. PMID 5001427 DOI: 10.1016/0006-8993(71)90360-X |
0.198 |
|
| 1993 |
Bailey A, Luthert P, Bolton P, Couteur AL, Rutter M, Harding B. Autism and megalencephaly The Lancet. 341: 1225-1226. PMID 8098126 DOI: 10.1016/0140-6736(93)91065-T |
0.193 |
|
| 2023 |
McCormick EM, Keller K, Taylor JP, Coffey AJ, Shen L, Krotoski D, Harding B, Alves CAPF, Ardissone A, Bai R, de Barcelos IP, Bertini E, Bluske K, Christodoulou J, Clause AR, et al. Expert panel curation of 113 primary mitochondrial disease genes for the Leigh syndrome spectrum. Annals of Neurology. PMID 37255483 DOI: 10.1002/ana.26716 |
0.158 |
|
| 2002 |
Turner JJ, Leotlela PD, Pannett AA, Forbes SA, Bassett JH, Harding B, Christie PT, Bowen-Jones D, Ellard S, Hattersley A, Jackson CE, Pope R, Quarrell OW, Trembath R, Thakker RV. Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1. The Journal of Clinical Endocrinology and Metabolism. 87: 2688-93. PMID 12050235 DOI: 10.1210/jcem.87.6.8607 |
0.155 |
|
| 2019 |
Surrey LF, Jain P, Zhang B, Straka J, Zhao X, Harding BN, Resnick AC, Storm PB, Buccoliero AM, Genitori L, Li MM, Waanders AJ, Santi M. Genomic Analysis of Dysembryoplastic Neuroepithelial Tumor Spectrum Reveals a Diversity of Molecular Alterations Dysregulating the MAPK and PI3K/mTOR Pathways. Journal of Neuropathology and Experimental Neurology. PMID 31617914 DOI: 10.1093/Jnen/Nlz101 |
0.142 |
|
| 2022 |
Boda E, Lorenzati M, Parolisi R, Harding B, Pallavicini G, Bonfanti L, Moccia A, Bielas S, Di Cunto F, Buffo A. Molecular and functional heterogeneity in dorsal and ventral oligodendrocyte progenitor cells of the mouse forebrain in response to DNA damage. Nature Communications. 13: 2331. PMID 35484145 DOI: 10.1038/s41467-022-30010-6 |
0.124 |
|
| 2021 |
Helman G, Zerem A, Almad A, Hacker JL, Woidill S, Sase S, LeFevre AN, Ekstein J, Johansson MM, Stutterd CA, Taft RJ, Simons C, Grinspan JB, Pizzino A, Schmidt JL, ... Harding B, et al. Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy. Pediatric Neurology. 121: 11-19. PMID 34111619 DOI: 10.1016/j.pediatrneurol.2021.04.014 |
0.121 |
|
| 1995 |
Harding BN, Ramani P, Thurley P. The familial syndrome of proliferative vasculopathy and hydranencephaly-hydrocephaly: immunocytochemical and ultrastructural evidence for endothelial proliferation. Neuropathology and Applied Neurobiology. 21: 61-7. PMID 7770122 |
0.109 |
|
| 1991 |
Tasker RC, Boyd SG, Harden A, Kendall B, Harding BN, Matthew DJ. The clinical significance of seizures in critically ill young infants requiring intensive care. Neuropediatrics. 22: 129-38. PMID 1944819 DOI: 10.1055/s-2008-1071431 |
0.1 |
|
| 2014 |
Russell AB, Wexler AG, Harding BN, Whitney JC, Bohn AJ, Goo YA, Tran BQ, Barry NA, Zheng H, Peterson SB, Chou S, Gonen T, Goodlett DR, Goodman AL, Mougous JD. A type VI secretion-related pathway in Bacteroidetes mediates interbacterial antagonism. Cell Host & Microbe. 16: 227-36. PMID 25070807 DOI: 10.1016/J.Chom.2014.07.007 |
0.096 |
|
| 2015 |
Chou S, Daugherty MD, Peterson SB, Biboy J, Yang Y, Jutras BL, Fritz-Laylin LK, Ferrin MA, Harding BN, Jacobs-Wagner C, Yang XF, Vollmer W, Malik HS, Mougous JD. Transferred interbacterial antagonism genes augment eukaryotic innate immune function. Nature. 518: 98-101. PMID 25470067 DOI: 10.1038/Nature13965 |
0.085 |
|
| 1979 |
Dodd PR, Hardy JA, Bradford HF, Bennett GW, Edwardson JA, Harding BN. Metabolic and secretory processes in nerve-endings isolated from post-mortem brain. Neuroscience Letters. 11: 87-92. PMID 431889 DOI: 10.1016/0304-3940(79)90051-X |
0.084 |
|
| 2014 |
Whitney JC, Beck CM, Goo YA, Russell AB, Harding BN, De Leon JA, Cunningham DA, Tran BQ, Low DA, Goodlett DR, Hayes CS, Mougous JD. Genetically distinct pathways guide effector export through the type VI secretion system. Molecular Microbiology. 92: 529-42. PMID 24589350 DOI: 10.1111/Mmi.12571 |
0.082 |
|
| 1984 |
Harding BN, Leonard JV, Erdohazi M. Ornithine carbamoyl transferase deficiency: a neuropathological study. European Journal of Pediatrics. 141: 215-20. PMID 6734670 |
0.08 |
|
| 2014 |
Pittman W, Han Z, Harding B, Rosas C, Jiang J, Pineda A, Mannan MS. Lessons to be learned from an analysis of ammonium nitrate disasters in the last 100 years. Journal of Hazardous Materials. 280: 472-7. PMID 25203808 DOI: 10.1016/j.jhazmat.2014.08.037 |
0.068 |
|
| 2008 |
Harding B, Torres-Harding S, Bond GR, Salyers MP, Rollins AL, Hardin T. Factors associated with early attrition from psychosocial rehabilitation programs. Community Mental Health Journal. 44: 283-8. PMID 18401713 DOI: 10.1007/S10597-008-9128-9 |
0.061 |
|
| 2006 |
Davis KE, Devitt T, Rollins A, O'Neill S, Pavick D, Harding B. Integrated residential treatment for persons with severe and persistent mental illness: lessons in recovery. Journal of Psychoactive Drugs. 38: 263-72. PMID 17165369 DOI: 10.1080/02791072.2006.10399852 |
0.061 |
|
| 1972 |
Harding BN. An electron microscope study of afferent fibre connexions to the monkey thalamus from motor cortex and basal ganglia. Journal of Anatomy. 111: 503-4. PMID 4627154 |
0.06 |
|
| 2011 |
Nahum JR, Harding BN, Kerr B. Evolution of restraint in a structured rock-paper-scissors community. Proceedings of the National Academy of Sciences of the United States of America. 108: 10831-8. PMID 21690371 DOI: 10.1073/Pnas.1100296108 |
0.047 |
|
| 2008 |
Fraser VV, Jones AM, Frounfelker R, Harding B, Hardin T, Bond GR. VR closure rates for two vocational models. Psychiatric Rehabilitation Journal. 31: 332-9. PMID 18407883 DOI: 10.2975/31.4.2008.332.339 |
0.043 |
|
| 2015 |
LeRoux M, Kirkpatrick RL, Montauti EI, Tran BQ, Peterson SB, Harding BN, Whitney JC, Russell AB, Traxler B, Goo YA, Goodlett DR, Wiggins PA, Mougous JD. Kin cell lysis is a danger signal that activates antibacterial pathways of Pseudomonas aeruginosa. Elife. 4. PMID 25643398 DOI: 10.7554/Elife.05701 |
0.034 |
|
| 1982 |
Valentine AR, Kendall BE, Harding BN. Computed tomography in acute haemorrhagic leukoencephalitis. Neuroradiology. 22: 215-9. PMID 7057996 |
0.029 |
|
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