The Neuropathology of FTD Associated With ALS : FTDMACKENZIE, Ian R. A.Alzheimer disease and associated disorders. 2007, Vol 21, Num 4, issn 0893-0341, S44-S49Article

Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrumMACKENZIE, Ian R. A; FELDMAN, Howard H.Journal of neuropathology and experimental neurology. 2005, Vol 64, Num 8, pp 730-739, issn 0022-3069, 10 p.Article

The molecular genetics and neuropathology of frontotemporal lobar degeneration : recent developmentsMACKENZIE, Ian R. A; RADEMAKERS, Rosa.Neurogenetics (Oxford. Print). 2007, Vol 8, Num 4, pp 237-248, issn 1364-6745, 12 p.Article

Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic casesMACKENZIE, Ian R. A; FELDMAN, Howard.Acta neuropathologica. 2003, Vol 105, Num 6, pp 543-548, issn 0001-6322, 6 p.Article

The relationship between extramotor ubiquitin-immunoreactive neuronal inclusions and dementia in motor neuron diseaseMACKENZIE, Ian R. A; FELDMAN, Howard.Acta neuropathologica. 2003, Vol 105, Num 2, pp 98-102, issn 0001-6322, 5 p.Article

Progranulin : normal function and role in neurodegenerationERIKSEN, Jason L; MACKENZIE, Ian R. A.Journal of neurochemistry. 2008, Vol 104, Num 2, pp 287-297, issn 0022-3042, 11 p.Article

Postmortem studies of the effect of anti-inflammatory drugs on Alzheimer-type pathology and associated inflammationMACKENZIE, Ian R. A.Neurobiology of aging. 2001, Vol 22, Num 6, pp 819-822, issn 0197-4580Article

A reassessment of the neuropathology of frontotemporal dementia linked to chromosome 3HOLM, Ida Elisabeth; ENGLUND, Elisabet; MACKENZIE, Ian R. A et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 10, pp 884-891, issn 0022-3069, 8 p.Article

rs5848 polymorphism and serum progranulin levelHSIUNG, Ging-Yuek R; FOK, Alice; FELDMAN, Howard H et al.Journal of the neurological sciences. 2011, Vol 300, Num 1-2, pp 28-32, issn 0022-510X, 5 p.Article

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43 -negative neuronal inclusionsMACKENZIE, Ian R. A; FOTI, Dean; WOULFE, John et al.Brain. 2008, Vol 131, pp 1282-1293, issn 0006-8950, 12 p., 5Article

The neuropathology and biochemistry of frontotemporal dementiaMUNOZ, David G; DICKSON, Dennis W; BERGERON, Catherine et al.Annals of neurology. 2003, Vol 54, pp S24-S28, issn 0364-5134, SUP5Conference Paper

Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9pHSIUNG, Ging-Yuek R; DEJESUS-HERNANDEZ, Mariely; BAKER, Matt et al.Brain. 2012, Vol 135, pp 709-722, issn 0006-8950, 14 p., 3Article

Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutationsMACKENZIE, Ian R. A; BIGIO, Eileen H; EISEN, Andrew et al.Annals of neurology. 2007, Vol 61, Num 5, pp 427-434, issn 0364-5134, 8 p.Article

FET proteins in frontotemporal dementia and amyotrophic lateral sclerosisMACKENZIE, Ian R. A; NEUMANN, Manuela.Brain research. 2012, Vol 1462, pp 40-43, issn 0006-8993, 4 p.Article

Superficial Siderosis : A Potential Diagnostic Marker of Cerebral Amyloid Angiopathy in Alzheimer DiseaseFELDMAN, Howard H; MAIA, Luis F; MACKENZIE, Ian R. A et al.Stroke (1970). 2008, Vol 39, Num 10, pp 2894-2897, issn 0039-2499, 4 p.Article

Mutations in progranulin explain atypical phenotypes with variants in MAPTPICKERING-BROWN, Stuart M; BAKER, Matt; KRIL, Jillian et al.Brain. 2006, Vol 129, pp 3124-3126, issn 0006-8950, 3 p., 11Article

FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutationsNEUMANN, Manuela; BENTMANN, Eva; YOKOTA, Osamu et al.Brain. 2011, Vol 134, pp 2595-2609, issn 0006-8950, 15 p., 9Article

Common variants at 7p21 are associated with fronto- temporal lobar degeneration with TDP-43 inclusionsVAN DEERLIN, Vivianna M; SLEIMAN, Patrick M. A; ARNOLD, Steven E et al.Nature genetics. 2010, Vol 42, Num 3, pp 234-239, issn 1061-4036, 6 p.Article

FUS GENE MUTATIONS IN FAMILIAL AND SPORADIC AMYOTROPHIC LATERAL SCLEROSISRADEMAKERS, Rosa; STEWART, Heather; DEJESUS-HERNANDEZ, Mariely et al.Muscle & nerve. 2010, Vol 42, Num 2, pp 170-176, issn 0148-639X, 7 p.Article

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin geneMACKENZIE, Ian R. A; BAKER, Matt; FELDMAN, Howard H et al.Brain. 2006, Vol 129, pp 3081-3090, issn 0006-8950, 10 p., 11Article

α-Internexin is present in the pathological inclusions of neuronal intermediate filament inclusion diseaseCAIRNS, Nigel J; ZHUKAREVA, Victoria; JAROS, Evelyn et al.The American journal of pathology. 2004, Vol 164, Num 6, pp 2153-2161, issn 0002-9440, 9 p.Article

Genetic and Clinical Features of Progranulin-Associated Frontotemporal Lobar DegenerationCHEN-PLOTKIN, Alice S; MARTINEZ-LAGE, Maria; WEINER, Myron F et al.Archives of neurology (Chicago). 2011, Vol 68, Num 4, pp 488-497, issn 0003-9942, 10 p.Article

A new subtype of frontotemporal lobar degeneration with FUS pathologyNEUMANN, Manuela; RADEMAKERS, Rosa; ROEBER, Sigrun et al.Brain. 2009, Vol 132, pp 2922-2931, issn 0006-8950, 10 p., 11Article

Clinical phenotypes of cerebral amyloid angiopathyMAIA, Luis F; MACKENZIE, Ian R. A; FELDMAN, Howard H et al.Journal of the neurological sciences. 2007, Vol 257, Num 1-2, pp 23-30, issn 0022-510X, 8 p.Conference Paper