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372 results

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Population screening for variant Creutzfeldt-Jakob disease using a novel blood test: diagnostic accuracy and feasibility study.
Jackson GS, Burk-Rafel J, Edgeworth JA, Sicilia A, Abdilahi S, Korteweg J, Mackey J, Thomas C, Wang G, Schott JM, Mummery C, Chinnery PF, Mead S, Collinge J. Jackson GS, et al. Among authors: schott jm. JAMA Neurol. 2014 Apr;71(4):421-8. doi: 10.1001/jamaneurol.2013.6001. JAMA Neurol. 2014. PMID: 24590363 Free PMC article. Clinical Trial.
The diagnosis of young-onset dementia.
Rossor MN, Fox NC, Mummery CJ, Schott JM, Warren JD. Rossor MN, et al. Among authors: schott jm. Lancet Neurol. 2010 Aug;9(8):793-806. doi: 10.1016/S1474-4422(10)70159-9. Lancet Neurol. 2010. PMID: 20650401 Free PMC article. Review.
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration.
Rohrer JD, Lashley T, Schott JM, Warren JE, Mead S, Isaacs AM, Beck J, Hardy J, de Silva R, Warrington E, Troakes C, Al-Sarraj S, King A, Borroni B, Clarkson MJ, Ourselin S, Holton JL, Fox NC, Revesz T, Rossor MN, Warren JD. Rohrer JD, et al. Among authors: schott jm. Brain. 2011 Sep;134(Pt 9):2565-81. doi: 10.1093/brain/awr198. Brain. 2011. PMID: 21908872 Free PMC article.
Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.
Beck J, Poulter M, Hensman D, Rohrer JD, Mahoney CJ, Adamson G, Campbell T, Uphill J, Borg A, Fratta P, Orrell RW, Malaspina A, Rowe J, Brown J, Hodges J, Sidle K, Polke JM, Houlden H, Schott JM, Fox NC, Rossor MN, Tabrizi SJ, Isaacs AM, Hardy J, Warren JD, Collinge J, Mead S. Beck J, et al. Among authors: schott jm. Am J Hum Genet. 2013 Mar 7;92(3):345-53. doi: 10.1016/j.ajhg.2013.01.011. Epub 2013 Feb 21. Am J Hum Genet. 2013. PMID: 23434116 Free PMC article.
Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.
Rohrer JD, Beck J, Plagnol V, Gordon E, Lashley T, Revesz T, Janssen JC, Fox NC, Warren JD, Rossor MN, Mead S, Schott JM. Rohrer JD, et al. Among authors: schott jm. J Neurol Neurosurg Psychiatry. 2013 Dec;84(12):1411-2. doi: 10.1136/jnnp-2013-306116. Epub 2013 Jul 31. J Neurol Neurosurg Psychiatry. 2013. PMID: 23904625 Free PMC article. No abstract available.
Validation of next-generation sequencing technologies in genetic diagnosis of dementia.
Beck J, Pittman A, Adamson G, Campbell T, Kenny J, Houlden H, Rohrer JD, de Silva R, Shoai M, Uphill J, Poulter M, Hardy J, Mummery CJ, Warren JD, Schott JM, Fox NC, Rossor MN, Collinge J, Mead S. Beck J, et al. Among authors: schott jm. Neurobiol Aging. 2014 Jan;35(1):261-5. doi: 10.1016/j.neurobiolaging.2013.07.017. Epub 2013 Aug 31. Neurobiol Aging. 2014. PMID: 23998997
Profiles of white matter tract pathology in frontotemporal dementia.
Mahoney CJ, Ridgway GR, Malone IB, Downey LE, Beck J, Kinnunen KM, Schmitz N, Golden HL, Rohrer JD, Schott JM, Rossor MN, Ourselin S, Mead S, Fox NC, Warren JD. Mahoney CJ, et al. Among authors: schott jm. Hum Brain Mapp. 2014 Aug;35(8):4163-79. doi: 10.1002/hbm.22468. Epub 2014 Feb 7. Hum Brain Mapp. 2014. PMID: 24510641 Free PMC article.
Altered body schema processing in frontotemporal dementia with C9ORF72 mutations.
Downey LE, Fletcher PD, Golden HL, Mahoney CJ, Agustus JL, Schott JM, Rohrer JD, Beck J, Mead S, Rossor MN, Crutch SJ, Warren JD. Downey LE, et al. Among authors: schott jm. J Neurol Neurosurg Psychiatry. 2014 Sep;85(9):1016-23. doi: 10.1136/jnnp-2013-306995. Epub 2014 Feb 12. J Neurol Neurosurg Psychiatry. 2014. PMID: 24521566 Free PMC article.
372 results