Revesz T - Search Results

1

Neurofilament inclusion body disease: a new proteinopathy?

Josephs KA, Holton JL, Rossor MN, Braendgaard H, Ozawa T, Fox NC, Petersen RC, Pearl GS, Ganguly M, Rosa P, Laursen H, Parisi JE, Waldemar G, Quinn NP, Dickson DW, Revesz T. Josephs KA, et al. Among authors: revesz t. Brain. 2003 Oct;126(Pt 10):2291-303. doi: 10.1093/brain/awg231. Epub 2003 Jul 22. Brain. 2003. PMID: 12876145

2

Frontotemporal lobar degeneration and ubiquitin immunohistochemistry.

Josephs KA, Holton JL, Rossor MN, Godbolt AK, Ozawa T, Strand K, Khan N, Al-Sarraj S, Revesz T. Josephs KA, et al. Among authors: revesz t. Neuropathol Appl Neurobiol. 2004 Aug;30(4):369-73. doi: 10.1111/j.1365-2990.2003.00545.x. Neuropathol Appl Neurobiol. 2004. PMID: 15305982

3

Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes: broadening the clinical picture to include progressive supranuclear palsy.

Paviour DC, Lees AJ, Josephs KA, Ozawa T, Ganguly M, Strand C, Godbolt A, Howard RS, Revesz T, Holton JL. Paviour DC, et al. Among authors: revesz t. Brain. 2004 Nov;127(Pt 11):2441-51. doi: 10.1093/brain/awh265. Epub 2004 Sep 30. Brain. 2004. PMID: 15459024

4

Magnetic resonance imaging signatures of tissue pathology in frontotemporal dementia.

Whitwell JL, Josephs KA, Rossor MN, Stevens JM, Revesz T, Holton JL, Al-Sarraj S, Godbolt AK, Fox NC, Warren JD. Whitwell JL, et al. Among authors: revesz t. Arch Neurol. 2005 Sep;62(9):1402-8. doi: 10.1001/archneur.62.9.1402. Arch Neurol. 2005. PMID: 16157747

5

A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies.

Lashley T, Rohrer JD, Bandopadhyay R, Fry C, Ahmed Z, Isaacs AM, Brelstaff JH, Borroni B, Warren JD, Troakes C, King A, Al-Saraj S, Newcombe J, Quinn N, Ostergaard K, Schrøder HD, Bojsen-Møller M, Braendgaard H, Fox NC, Rossor MN, Lees AJ, Holton JL, Revesz T. Lashley T, et al. Among authors: revesz t. Brain. 2011 Sep;134(Pt 9):2548-64. doi: 10.1093/brain/awr160. Epub 2011 Jul 12. Brain. 2011. PMID: 21752791 Free PMC article.

6

A case of sporadic Pick disease with onset at 27 years.

Jacob J, Revesz T, Thom M, Rossor MN. Jacob J, et al. Among authors: revesz t. Arch Neurol. 1999 Oct;56(10):1289-91. doi: 10.1001/archneur.56.10.1289. Arch Neurol. 1999. PMID: 10520947

7

Semantic dementia with ubiquitin-positive tau-negative inclusion bodies.

Rossor MN, Revesz T, Lantos PL, Warrington EK. Rossor MN, et al. Among authors: revesz t. Brain. 2000 Feb;123 ( Pt 2):267-76. doi: 10.1093/brain/123.2.267. Brain. 2000. PMID: 10648435

8

Evidence for pathological involvement of the spinal cord in motor neuron disease-inclusion dementia.

Holton JL, Révész T, Crooks R, Scaravilli F. Holton JL, et al. Among authors: revesz t. Acta Neuropathol. 2002 Mar;103(3):221-7. doi: 10.1007/s004010100457. Epub 2001 Nov 10. Acta Neuropathol. 2002. PMID: 11907801

9

Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.

Janssen JC, Warrington EK, Morris HR, Lantos P, Brown J, Revesz T, Wood N, Khan MN, Cipolotti L, Fox NC, Rossor MN. Janssen JC, et al. Among authors: revesz t. Neurology. 2002 Apr 23;58(8):1161-8. doi: 10.1212/wnl.58.8.1161. Neurology. 2002. PMID: 11971081

10

Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP.

Morris HR, Osaki Y, Holton J, Lees AJ, Wood NW, Revesz T, Quinn N. Morris HR, et al. Among authors: revesz t. Neurology. 2003 Jul 8;61(1):102-4. doi: 10.1212/01.wnl.0000072325.27824.a5. Neurology. 2003. PMID: 12847166

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