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Items: 1 to 50 of 64

1.

The MIGHTI Wind Retrieval Algorithm: Description and Verification.

Harding BJ, Makela JJ, Englert CR, Marr KD, Harlander JM, England SL, Immel TJ.

Space Sci Rev. 2017 Oct;212(1-2):585-600. doi: 10.1007/s11214-017-0359-3. Epub 2017 Apr 10.

PMID:
30034033
2.

Michelson Interferometer for Global High-resolution Thermospheric Imaging (MIGHTI): Instrument Design and Calibration.

Englert CR, Harlander JM, Brown CM, Marr KD, Miller IJ, Stump JE, Hancock J, Peterson JQ, Kumler J, Morrow WH, Mooney TA, Ellis S, Mende SB, Harris SE, Stevens MH, Makela JJ, Harding BJ, Immel TJ.

Space Sci Rev. 2017 Oct;212(1-2):553-584. doi: 10.1007/s11214-017-0358-4. Epub 2017 Apr 20.

PMID:
30008488
3.

Novel FGFR2-INA fusion identified in two low-grade mixed neuronal-glial tumors drives oncogenesis via MAPK and PI3K/mTOR pathway activation.

Jain P, Surrey LF, Straka J, Luo M, Lin F, Harding B, Resnick AC, Storm PB, Buccoliero AM, Santi M, Li MM, Waanders AJ.

Acta Neuropathol. 2018 May 16. doi: 10.1007/s00401-018-1864-5. [Epub ahead of print] No abstract available.

4.

Adult Human Hippocampus: No New Neurons in Sight.

Arellano JI, Harding B, Thomas JL.

Cereb Cortex. 2018 Jul 1;28(7):2479-2481. doi: 10.1093/cercor/bhy106.

PMID:
29746611
5.

Clinical Reasoning: A 12-year-old girl with headache and change in mental status.

Patel P, Ross A, Henretig FM, Liu G, Harding B, Panzer J.

Neurology. 2018 Mar 13;90(11):524-529. doi: 10.1212/WNL.0000000000005116. No abstract available.

PMID:
29530960
6.

Developmental and perinatal brain diseases.

Adle-Biassette H, Golden JA, Harding B.

Handb Clin Neurol. 2017;145:51-78. doi: 10.1016/B978-0-12-802395-2.00006-7. Review.

PMID:
28987191
7.

Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons.

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.

Am J Hum Genet. 2016 Aug 4;99(2):511-20. doi: 10.1016/j.ajhg.2016.07.003. Epub 2016 Jul 21.

8.

Degos disease mimicking primary vasculitis of the CNS.

Gmuca S, Boos MD, Treece A, Narula S, Billinghurst L, Bhatti T, Laje P, Perman MJ, Vossough A, Harding B, Burnham J, Banwell B.

Neurol Neuroimmunol Neuroinflamm. 2016 Feb 2;3(2):e206. doi: 10.1212/NXI.0000000000000206. eCollection 2016 Apr. No abstract available.

9.

Case study and lessons learned from the ammonium nitrate explosion at the West Fertilizer facility.

Laboureur DM, Han Z, Harding BZ, Pineda A, Pittman WC, Rosas C, Jiang J, Mannan MS.

J Hazard Mater. 2016 May 5;308:164-72. doi: 10.1016/j.jhazmat.2016.01.039. Epub 2016 Jan 18.

PMID:
26812084
10.

A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease.

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.

PLoS One. 2016 Jan 6;11(1):e0145500. doi: 10.1371/journal.pone.0145500. eCollection 2016.

11.

Clinical and histopathological outcomes in patients with SCN1A mutations undergoing surgery for epilepsy.

Skjei KL, Church EW, Harding BN, Santi M, Holland-Bouley KD, Clancy RR, Porter BE, Heuer GG, Marsh ED.

J Neurosurg Pediatr. 2015 Dec;16(6):668-74. doi: 10.3171/2015.5.PEDS14551. Epub 2015 Sep 4.

PMID:
26339958
12.

Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73.

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, Cross H, Harlalka GV, Hurles ME, Maroofian R, Heaps AD, Morton MC, Stempak L, Hildebrandt F, Sadowski CE, Zaritsky J, Campellone K, Morton DH, Wang H, Crosby A, Strauss KA.

Brain. 2015 Aug;138(Pt 8):2173-90. doi: 10.1093/brain/awv153. Epub 2015 Jun 11.

13.

Spectrum of neuropathophysiology in spinal muscular atrophy type I.

Harding BN, Kariya S, Monani UR, Chung WK, Benton M, Yum SW, Tennekoon G, Finkel RS.

J Neuropathol Exp Neurol. 2015 Jan;74(1):15-24. doi: 10.1097/NEN.0000000000000144.

14.

Lessons to be learned from an analysis of ammonium nitrate disasters in the last 100 years.

Pittman W, Han Z, Harding B, Rosas C, Jiang J, Pineda A, Mannan MS.

J Hazard Mater. 2014 Sep 15;280:472-7. doi: 10.1016/j.jhazmat.2014.08.037. Epub 2014 Aug 29. Review.

PMID:
25203808
15.

Chromosome band 7q34 deletions resulting in KIAA1549-BRAF and FAM131B-BRAF fusions in pediatric low-grade Gliomas.

Roth JJ, Santi M, Pollock AN, Harding BN, Rorke-Adams LB, Tooke LS, Biegel JA.

Brain Pathol. 2015 Mar;25(2):182-92. doi: 10.1111/bpa.12167. Epub 2014 Sep 12.

16.

Diagnostic application of high resolution single nucleotide polymorphism array analysis for children with brain tumors.

Roth JJ, Santi M, Rorke-Adams LB, Harding BN, Busse TM, Tooke LS, Biegel JA.

Cancer Genet. 2014 Apr;207(4):111-23. doi: 10.1016/j.cancergen.2014.03.002. Epub 2014 Mar 15.

17.

Nonlinear regression method for estimating neutral wind and temperature from Fabry-Perot interferometer data.

Harding BJ, Gehrels TW, Makela JJ.

Appl Opt. 2014 Feb 1;53(4):666-73. doi: 10.1364/AO.53.000666.

PMID:
24514183
18.

Imaging findings of patients with metastatic neuroblastoma to the brain.

Nabavizadeh SA, Feygin T, Harding BN, Bilaniuk LT, Zimmerman RA, Vossough A.

Acad Radiol. 2014 Mar;21(3):329-37. doi: 10.1016/j.acra.2013.10.016. Epub 2013 Dec 22.

PMID:
24365052
19.

Epigenetic genome-wide analysis identifies BEX1 as a candidate tumour suppressor gene in paediatric intracranial ependymoma.

Karakoula K, Jacques TS, Phipps KP, Harkness W, Thompson D, Harding BN, Darling JL, Warr TJ.

Cancer Lett. 2014 Apr 28;346(1):34-44. doi: 10.1016/j.canlet.2013.12.005. Epub 2013 Dec 11.

PMID:
24333734
20.

Brain tumor presenting as somnambulism in an adolescent.

Prashad PS, Marcus CL, Brown LW, Dlugos DJ, Feygin T, Harding BN, Heuer GG, Mason TB.

Pediatr Neurol. 2013 Sep;49(3):209-12. doi: 10.1016/j.pediatrneurol.2013.04.022. Epub 2013 Jul 5.

PMID:
23835274
21.

Receptor-mediated endocytosis and endosomal acidification is impaired in proximal tubule epithelial cells of Dent disease patients.

Gorvin CM, Wilmer MJ, Piret SE, Harding B, van den Heuvel LP, Wrong O, Jat PS, Lippiat JD, Levtchenko EN, Thakker RV.

Proc Natl Acad Sci U S A. 2013 Apr 23;110(17):7014-9. doi: 10.1073/pnas.1302063110. Epub 2013 Apr 9.

22.

Proliferation rates of multiple endocrine neoplasia type 1 (MEN1)-associated tumors.

Walls GV, Reed AA, Jeyabalan J, Javid M, Hill NR, Harding B, Thakker RV.

Endocrinology. 2012 Nov;153(11):5167-79. doi: 10.1210/en.2012-1675. Epub 2012 Sep 28.

23.

MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary adenomas.

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.

Cancer Res. 2012 Oct 1;72(19):5060-8. doi: 10.1158/0008-5472.CAN-12-1821. Epub 2012 Aug 21.

24.

Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites.

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, Burren C, Connell JM, Jung H, Marks E, McCredie D, Mughal Z, Rodda C, Tollefsen S, Brown EM, Yang JJ, Thakker RV.

Hum Mol Genet. 2012 Jun 15;21(12):2768-78. doi: 10.1093/hmg/dds105. Epub 2012 Mar 14.

PMID:
22422767
25.

Cortical malformations: unfolding polymicrogyria.

Golden JA, Harding BN.

Nat Rev Neurol. 2010 Sep;6(9):471-2. doi: 10.1038/nrneurol.2010.118. No abstract available.

PMID:
20811463
26.

Balloon cells in human cortical dysplasia and tuberous sclerosis: isolation of a pathological progenitor-like cell.

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.

Acta Neuropathol. 2010 Jul;120(1):85-96. doi: 10.1007/s00401-010-0677-y. Epub 2010 Mar 30.

PMID:
20352236
27.

Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisation.

Ward SJ, Karakoula K, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Darling JL, Thomas DG, Warr TJ.

J Neurooncol. 2010 Jul;98(3):305-18. doi: 10.1007/s11060-009-0081-4. Epub 2010 Jan 6.

PMID:
20052518
28.

Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia.

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.

Endocr Relat Cancer. 2009 Dec;16(4):1313-27. doi: 10.1677/ERC-09-0082. Epub 2009 Jul 20.

29.

Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiers.

Lemos MC, Harding B, Reed AA, Jeyabalan J, Walls GV, Bowl MR, Sharpe J, Wedden S, Moss JE, Ross A, Davidson D, Thakker RV.

J Endocrinol. 2009 Oct;203(1):133-42. doi: 10.1677/JOE-09-0124. Epub 2009 Jul 8.

30.

Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytoma.

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.

Neoplasia. 2008 Aug;10(8):757-72.

31.

Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13.

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.

Genes Chromosomes Cancer. 2008 Nov;47(11):1005-22. doi: 10.1002/gcc.20607.

PMID:
18663750
32.

VR closure rates for two vocational models.

Fraser VV, Jones AM, Frounfelker R, Harding B, Hardin T, Bond GR.

Psychiatr Rehabil J. 2008 Spring;31(4):332-9. doi: 10.2975/31.4.2008.332.339.

PMID:
18407883
33.

Factors associated with early attrition from psychosocial rehabilitation programs.

Harding B, Torres-Harding S, Bond GR, Salyers MP, Rollins AL, Hardin T.

Community Ment Health J. 2008 Aug;44(4):283-8. doi: 10.1007/s10597-008-9128-9. Epub 2008 Apr 10.

PMID:
18401713
34.

Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.

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, Crandall B, Lauzon JL, Viskochil DH, Harding B, Graham JM Jr.

Am J Med Genet A. 2007 Dec 15;143A(24):2981-3008.

PMID:
18000912
35.

An investigation of the expression of G1-phase cell cycle proteins in focal cortical dysplasia type IIB.

Thom M, Martinian L, Sen A, Squier W, Harding BN, Cross JH, Harkness W, McEvoy A, Sisodiya SM.

J Neuropathol Exp Neurol. 2007 Nov;66(11):1045-55.

PMID:
17984686
36.

International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trials.

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, Rushing EJ, Sewry C, Charman SC, Pilkington CA, Holton JL; UK Juvenile Dermatomyositis Research Group.

Arthritis Rheum. 2007 Oct 15;57(7):1192-201.

37.

Quantification of normal range of inflammatory changes in morphologically normal pediatric muscle.

Varsani H, Newton KR, Li CK, Harding B, Holton JL, Wedderburn LR.

Muscle Nerve. 2008 Feb;37(2):259-61.

PMID:
17847070
38.

Pathological tau tangles localize to focal cortical dysplasia in older patients.

Sen A, Thom M, Martinian L, Harding B, Cross JH, Nikolic M, Sisodiya SM.

Epilepsia. 2007 Aug;48(8):1447-54. Epub 2007 Apr 18.

39.

A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1.

Lemos MC, Harding B, Shalet SM, Thakker RV.

Clin Endocrinol (Oxf). 2007 May;66(5):709-13. Epub 2007 Mar 27.

PMID:
17388795
40.

Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor.

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, Halac I, Hendy GN, Lalloo F, Mache CJ, Mughal Z, Ong AC, Rinat C, Shaw N, Smithson SF, Tolmie J, Weill J, Nesbit MA, Thakker RV.

Hum Mol Genet. 2007 Feb 1;16(3):265-75. Epub 2007 Jan 8.

PMID:
17210674
41.

Integrated residential treatment for persons with severe and persistent mental illness: lessons in recovery.

Davis KE, Devitt T, Rollins A, O'Neill S, Pavick D, Harding B.

J Psychoactive Drugs. 2006 Sep;38(3):263-72.

PMID:
17165369
42.

Functional characterization of calcium sensing receptor polymorphisms and absence of association with indices of calcium homeostasis and bone mineral density.

Harding B, Curley AJ, Hannan FM, Christie PT, Bowl MR, Turner JJ, Barber M, Gillham-Nasenya I, Hampson G, Spector TD, Thakker RV.

Clin Endocrinol (Oxf). 2006 Nov;65(5):598-605.

PMID:
17054460
43.

Hippocampal sclerosis in children with lesional epilepsy is influenced by age at seizure onset.

Riney CJ, Harding B, Harkness WJ, Scott RC, Cross JH.

Epilepsia. 2006 Jan;47(1):159-66.

44.

Taylor-type focal cortical dysplasia in infants: some MRI lesions almost disappear with maturation of myelination.

Eltze CM, Chong WK, Bhate S, Harding B, Neville BG, Cross JH.

Epilepsia. 2005 Dec;46(12):1988-92.

45.

MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO).

Kennedy AM, Inada M, Krane SM, Christie PT, Harding B, López-Otín C, Sánchez LM, Pannett AA, Dearlove A, Hartley C, Byrne MH, Reed AA, Nesbit MA, Whyte MP, Thakker RV.

J Clin Invest. 2005 Oct;115(10):2832-42.

46.

An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism.

Bowl MR, Nesbit MA, Harding B, Levy E, Jefferson A, Volpi E, Rizzoti K, Lovell-Badge R, Schlessinger D, Whyte MP, Thakker RV.

J Clin Invest. 2005 Oct;115(10):2822-31. Epub 2005 Sep 15.

47.

Spontaneous regression of residual low-grade cerebellar pilocytic astrocytomas in children.

Gunny RS, Hayward RD, Phipps KP, Harding BN, Saunders DE.

Pediatr Radiol. 2005 Nov;35(11):1086-91. Epub 2005 Jul 27.

PMID:
16047140
48.

A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosis.

Lemos MC, Kotanko P, Christie PT, Harding B, Javor T, Smith C, Eastell R, Thakker RV.

J Clin Endocrinol Metab. 2005 Sep;90(9):5386-92. Epub 2005 Jun 28.

PMID:
15985493
49.

X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase.

Andrew Nesbit M, Bowl MR, Harding B, Schlessinger D, Whyte MP, Thakker RV.

Genomics. 2004 Dec;84(6):1060-70.

PMID:
15533723
50.

Acute fulminant subacute sclerosing panencephalitis with absent measles and PCR studies in cerebrospinal fluid.

Chung BH, Ip PP, Wong VC, Lo JY, Harding B.

Pediatr Neurol. 2004 Sep;31(3):222-4.

PMID:
15351025

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