| Year |
Citation |
Score |
| 2020 |
Stehmann C, Senesi M, Sarros S, McGlade A, Simpson M, Klug G, McLean C, Masters CL, Collins S. Creutzfeldt-Jakob disease surveillance in Australia: update to 31 December 2019. Communicable Diseases Intelligence (2018). 44. PMID 32664829 DOI: 10.33321/Cdi.2020.44.56 |
0.319 |
|
| 2020 |
Gao Y, Wilson GR, Stephenson SEM, Oulad-Abdelghani M, Charlet-Berguerand N, Bozaoglu K, McLean CA, Thomas PQ, Finkelstein DI, Lockhart PJ. Distribution of Parkinson's disease associated RAB39B in mouse brain tissue. Molecular Brain. 13: 52. PMID 32228644 DOI: 10.1186/S13041-020-00584-7 |
0.301 |
|
| 2019 |
Grubman A, Chew G, Ouyang JF, Sun G, Choo XY, McLean C, Simmons RK, Buckberry S, Vargas-Landin DB, Poppe D, Pflueger J, Lister R, Rackham OJL, Petretto E, Polo JM. A single-cell atlas of entorhinal cortex from individuals with Alzheimer's disease reveals cell-type-specific gene expression regulation. Nature Neuroscience. PMID 31768052 DOI: 10.1038/S41593-019-0539-4 |
0.305 |
|
| 2019 |
Cali CP, Patino M, Tai YK, Ho WY, McLean CA, Morris CM, Seeley WW, Miller BL, Gaig C, Vonsattel JPG, White CL, Roeber S, Kretzschmar H, Troncoso JC, Troakes C, et al. C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy. Acta Neuropathologica. PMID 31327044 DOI: 10.1007/S00401-019-02045-5 |
0.338 |
|
| 2019 |
Slade CA, McLean C, Scerri T, Giang TB, Megaloudis S, Strathmore A, Tempany JC, Nicholls K, D'Arcy C, Bahlo M, Hodgkin PD, Douglass JA, Bryant VL. Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2. Journal of Clinical Immunology. PMID 30927119 DOI: 10.1007/S10875-019-00602-X |
0.341 |
|
| 2018 |
Cali I, Cohen ML, Haїk S, Parchi P, Giaccone G, Collins SJ, Kofskey D, Wang H, McLean CA, Brandel JP, Privat N, Sazdovitch V, Duyckaerts C, Kitamoto T, Belay ED, et al. Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study. Acta Neuropathologica Communications. 6: 5. PMID 29310723 DOI: 10.1186/S40478-017-0503-Z |
0.323 |
|
| 2017 |
von Jonquieres G, Spencer ZHT, Rowlands BD, Klugmann CB, Bongers A, Harasta AE, Parley KE, Cederholm J, Teahan O, Pickford R, Delerue F, Ittner LM, Fröhlich D, McLean CA, Don AS, et al. Uncoupling N-acetylaspartate from brain pathology: implications for Canavan disease gene therapy. Acta Neuropathologica. PMID 29116375 DOI: 10.1007/S00401-017-1784-9 |
0.315 |
|
| 2017 |
Rita Cardoso B, Hare DJ, Lind M, McLean CA, Volitakis I, Laws SM, Masters CL, Bush AI, Roberts BR. The APOE ε4 allele is associated with lower selenium levels in the brain: implications in Alzheimer's disease. Acs Chemical Neuroscience. PMID 28453930 DOI: 10.1021/Acschemneuro.7B00014 |
0.308 |
|
| 2016 |
Roberts BR, Doecke JD, Rembach A, Yévenes LF, Fowler CJ, McLean CA, Lind M, Volitakis I, Masters CL, Bush AI, Hare DJ. Rubidium and potassium levels are altered in Alzheimer's disease brain and blood but not in cerebrospinal fluid. Acta Neuropathologica Communications. 4: 119. PMID 27842602 DOI: 10.1186/S40478-016-0390-8 |
0.306 |
|
| 2016 |
Byrne S, Jansen L, U-King-Im JM, Siddiqui A, Lidov HG, Bodi I, Smith L, Mein R, Cullup T, Dionisi-Vici C, Al-Gazali L, Al-Owain M, Bruwer Z, Al Thihli K, El-Garhy R, ... ... McLean CA, et al. EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy. Brain : a Journal of Neurology. 139: 765-81. PMID 26917586 DOI: 10.1093/Brain/Awv393 |
0.308 |
|
| 2015 |
Cairns NJ, Perrin RJ, Franklin EE, Carter D, Vincent B, Xie M, Bateman RJ, Benzinger T, Friedrichsen K, Brooks WS, Halliday GM, McLean C, Ghetti B, Morris JC, et al. Neuropathologic assessment of participants in two multi-center longitudinal observational studies: The Alzheimer Disease Neuroimaging Initiative (ADNI) and the Dominantly Inherited Alzheimer Network (DIAN). Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 25964057 DOI: 10.1111/Neup.12205 |
0.317 |
|
| 2014 |
Wilson GR, Sim JC, McLean C, Giannandrea M, Galea CA, Riseley JR, Stephenson SE, Fitzpatrick E, Haas SA, Pope K, Hogan KJ, Gregg RG, Bromhead CJ, Wargowski DS, Lawrence CH, et al. Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology. American Journal of Human Genetics. 95: 729-35. PMID 25434005 DOI: 10.1016/J.Ajhg.2014.10.015 |
0.311 |
|
| 2014 |
Adlard PA, Li QX, McLean C, Masters CL, Bush AI, Fodero-Tavoletti M, Villemagne V, Barnham KJ. β-amyloid in biological samples: not all Aβ detection methods are created equal. Frontiers in Aging Neuroscience. 6: 203. PMID 25165449 DOI: 10.3389/Fnagi.2014.00203 |
0.306 |
|
| 2013 |
Simpson M, Johanssen V, Boyd A, Klug G, Masters CL, Li QX, Pamphlett R, McLean C, Lewis V, Collins SJ. Unusual clinical and molecular-pathological profile of gerstmann-Sträussler-Scheinker disease associated with a novel PRNP mutation (V176G). Jama Neurology. 70: 1180-5. PMID 23857164 DOI: 10.1001/Jamaneurol.2013.165 |
0.341 |
|
| 2013 |
Lee W, Simpson M, Ling H, McLean C, Collins S, Williams DR. Characterising the uncommon corticobasal syndrome presentation of sporadic Creutzfeldt-Jakob disease. Parkinsonism & Related Disorders. 19: 81-5. PMID 22943965 DOI: 10.1016/J.Parkreldis.2012.07.010 |
0.331 |
|
| 2012 |
Lei P, Ayton S, Finkelstein DI, Spoerri L, Ciccotosto GD, Wright DK, Wong BX, Adlard PA, Cherny RA, Lam LQ, Roberts BR, Volitakis I, Egan GF, McLean CA, Cappai R, et al. Tau deficiency induces parkinsonism with dementia by impairing APP-mediated iron export. Nature Medicine. 18: 291-5. PMID 22286308 DOI: 10.1038/Nm.2613 |
0.303 |
|
| 2012 |
Liberski PP, Sikorska B, Lindenbaum S, Goldfarb LG, McLean C, Hainfellner JA, Brown P. Kuru: genes, cannibals and neuropathology. Journal of Neuropathology and Experimental Neurology. 71: 92-103. PMID 22249461 DOI: 10.1097/Nen.0B013E3182444Efd |
0.319 |
|
| 2011 |
Masters CL, Kril JJ, Halliday GM, Pamphlett R, Collins S, Hill AF, McLean C. Overview and recent advances in neuropathology. Part 2: Neurodegeneration. Pathology. 43: 93-102. PMID 21233670 DOI: 10.1097/Pat.0B013E3283426Eee |
0.326 |
|
| 2011 |
McLean C. Creutzfeldt-Jakob disease Pathology. 43. DOI: 10.1016/S0031-3025(16)33139-7 |
0.316 |
|
| 2011 |
McLean C. Neuropathology masterclass – a practical approach to the diagnosis of non-tumour pathology Pathology. 43. DOI: 10.1016/S0031-3025(16)33096-3 |
0.326 |
|
| 2009 |
Fodero-Tavoletti MT, Cappai R, McLean CA, Pike KE, Adlard PA, Cowie T, Connor AR, Masters CL, Rowe CC, Villemagne VL. Amyloid imaging in Alzheimer's disease and other dementias. Brain Imaging and Behavior. 3: 246-61. PMID 22005989 DOI: 10.1007/S11682-009-9067-2 |
0.302 |
|
| 2007 |
Rowe DB, Lewis V, Needham M, Rodriguez M, Boyd A, McLean C, Roberts H, Masters CL, Collins SJ. Novel prion protein gene mutation presenting with subacute PSP-like syndrome. Neurology. 68: 868-70. PMID 17353478 DOI: 10.1212/01.Wnl.0000256819.61531.98 |
0.3 |
|
| 2004 |
Poljak A, McLean CA, Sachdev P, Brodaty H, Smythe GA. Quantification of hemorphins in Alzheimer's disease brains. Journal of Neuroscience Research. 75: 704-14. PMID 14991846 DOI: 10.1002/Jnr.20020 |
0.303 |
|
| 2003 |
Miklossy J, Taddei K, Suva D, Verdile G, Fonte J, Fisher C, Gnjec A, Ghika J, Suard F, Mehta PD, McLean CA, Masters CL, Brooks WS, Martins RN. Two novel presenilin-1 mutations (Y256S and Q222H) are associated with early-onset Alzheimer's disease. Neurobiology of Aging. 24: 655-62. PMID 12885573 DOI: 10.1016/S0197-4580(02)00192-6 |
0.315 |
|
| 2002 |
Halliday G, Ng T, Rodriguez M, Harding A, Blumbergs P, Evans W, Fabian V, Fryer J, Gonzales M, Harper C, Kalnins R, Masters CL, McLean C, Milder DG, Pamphlett R, et al. Consensus neuropathological diagnosis of common dementia syndromes: testing and standardising the use of multiple diagnostic criteria. Acta Neuropathologica. 104: 72-8. PMID 12070667 DOI: 10.1007/S00401-002-0529-5 |
0.314 |
|
| 2001 |
Fodero LR, Sáez-Valero J, Barquero MS, Marcos A, McLean CA, Small DH. Wheat germ agglutinin-binding glycoproteins are decreased in Alzheimer's disease cerebrospinal fluid. Journal of Neurochemistry. 79: 1022-6. PMID 11739614 DOI: 10.1046/J.1471-4159.2001.00640.X |
0.306 |
|
| 2001 |
Collins S, McLean CA, Masters CL. Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 8: 387-97. PMID 11535002 DOI: 10.1054/Jocn.2001.0919 |
0.343 |
|
| 2000 |
Sáez-Valero J, Barquero MS, Marcos A, McLean CA, Small DH. Altered glycosylation of acetylcholinesterase in lumbar cerebrospinal fluid of patients with Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 69: 664-7. PMID 11032625 DOI: 10.1136/Jnnp.69.5.664 |
0.311 |
|
| 2000 |
Collins S, Boyd A, Fletcher A, Byron K, Harper C, McLean CA, Masters CL. Novel prion protein gene mutation in an octogenarian with Creutzfeldt-Jakob disease. Archives of Neurology. 57: 1058-63. PMID 10891990 DOI: 10.1001/Archneur.57.7.1058 |
0.342 |
|
| 2000 |
Collins S, Boyd A, Fletcher A, Gonzales M, McLean CA, Byron K, Masters CL. Creutzfeldt-Jakob disease: diagnostic utility of 14-3-3 protein immunodetection in cerebrospinal fluid. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 7: 203-8. PMID 10833616 DOI: 10.1054/Jocn.1999.0193 |
0.311 |
|
| 2000 |
Collins S, Boyd A, Fletcher A, Gonzales MF, McLean CA, Masters CL. Recent advances in the pre-mortem diagnosis of Creutzfeldt-Jakob disease. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 7: 195-202. PMID 10833615 DOI: 10.1054/Jocn.1999.0191 |
0.314 |
|
| 1997 |
McLean CA, Beyreuther K, Masters CL. Commentary on the consensus recommendations for the post mortem diagnosis of Alzheimer's disease. Neurobiology of Aging. 18: S89-90. PMID 9330993 DOI: 10.1016/S0197-4580(97)00061-4 |
0.304 |
|
| 1997 |
Sáez-Valero J, Sberna G, McLean CA, Masters CL, Small DH. Glycosylation of acetylcholinesterase as diagnostic marker for Alzheimer's disease. Lancet (London, England). 350: 929. PMID 9314873 DOI: 10.1016/S0140-6736(97)24039-0 |
0.322 |
|
| 1995 |
Niekrash RE, McLean CA, Kaye AH, Hjorth R, Desmond PM, Sinicaks V, Gonzales MF. Rapidly progressive Whipple's disease of the central nervous system Journal of Clinical Neuroscience. 2: 171-176. DOI: 10.1016/0967-5868(95)90013-6 |
0.314 |
|
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