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Cellular and Molecular Life Sciences : CMLS|November 10, 2009
Cerebral amyloidosis: amyloid subunits, mutants and phenotypesA Rostagno, J L Holton, T Lashley, et al.
Neuropathology and Applied Neurobiology|April 2, 2025
Pathological Characterisation of Posterior Cortical Atrophy in Comparison With Amnestic Alzheimer's DiseaseZ Abdi, K X Yong, J M Schott, et al.
Cellular and Molecular Life Sciences : CMLS|June 22, 2005
Chromosome 13 dementiasA Rostagno, Y Tomidokoro, T Lashley, et al.
Brain Pathology (Zurich, Switzerland)|April 15, 2006
Genetic alterations of the BRI2 gene: familial British and Danish dementiasJ Ghiso, A Rostagno, Y Tomidokoro, et al.
Pediatric Hematology and Oncology|January 1, 1996
History and current state of pediatric oncology and hematology in the United Arab EmiratesC Mpofu, T Revesz
Neuropathology and Applied Neurobiology|February 20, 2008
Expression of BRI2 mRNA and protein in normal human brain and familial British dementia: its relevance to the pathogenesis of diseaseT Lashley, T Revesz, G Plant, et al.
Neuropathology and Applied Neurobiology|November 10, 2007
Proposed neuropathological criteria for the post mortem diagnosis of multiple system atrophyJ Q Trojanowski, T Revesz,
Brain : a Journal of Neurology|April 19, 2002
Pathological, clinical and genetic heterogeneity in progressive supranuclear palsyH R Morris, G Gibb, R Katzenschlager, et al.
The Journal of Biological Chemistry|September 15, 2001
Systemic amyloid deposits in familial British dementiaJ A Ghiso, J Holton, L Miravalle, et al.
Neuropathology and Applied Neurobiology|September 16, 2006
Molecular chaperons, amyloid and preamyloid lesions in the BRI2 gene-related dementias: a morphological studyT Lashley, J L Holton, M M Verbeek, et al.
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