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Regional differences in the Purkinje cells settled pattern: A comparative autoradiographic study in control and homozygous weaver miceMARTI, Joaquin; WILLS, Katherine V; GHETTI, Bernardino et al.Experimental neurology (Print). 2002, Vol 175, Num 1, pp 168-181, issn 0014-4886Article

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Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroidsRADEMAKERS, Rosa; BAKER, Matt; ADAMSON, Jennifer et al.Nature genetics. 2012, Vol 44, Num 2, pp 200-205, issn 1061-4036, 6 p.Article

Failure to Detect the Presence of Prions in the Uterine and Gestational Tissues from a Gravida with Creutzfeldt-Jakob DiseaseXIANGZHU XIAO; MIRAVALLE, Leticia; QINGZHONG KONG et al.The American journal of pathology. 2009, Vol 174, Num 5, pp 1602-1608, issn 0002-9440, 7 p.Article

The ε isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann -Sträussler -Scheinker diseaseDI FEDE, Giuseppe; GIACCONE, Giorgio; LIMIDO, Lucia et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 2, pp 124-130, issn 0022-3069, 7 p.Article

Performance on MMSE sub-items and education level in presenilin-1 mutation carriers without dementiaRINGMAN, John M; RODRIGUEZ, Yaneth; MURRELL, Jill et al.International psychogeriatrics. 2007, Vol 19, Num 2, pp 323-332, issn 1041-6102, 10 p.Article

Symptom onset in autosomal dominant Alzheimer disease: A systematic review and meta-analysisRYMAN, Davis C; ACOSTA-BAENA, Natalia; LOPERA, Francisco et al.Neurology. 2014, Vol 83, Num 3, pp 253-260, issn 0028-3878, 8 p.Article

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Familial Prion Disease with Alzheimer Disease-Like Tau Pathology and Clinical PhenotypeJAYADEV, Suman; NOCHLIN, David; POORKAJ, Parvoneh et al.Annals of neurology. 2011, Vol 69, Num 4, pp 712-720, issn 0364-5134, 9 p.Article

Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted diseasePARCHI, Piero; CESCATTI, Maura; NOTARI, Silvio et al.Brain. 2010, Vol 133, pp 3030-3042, issn 0006-8950, 13 p., 10Article

SNARE protein redistribution and synaptic failure in a transgenic mouse model of Parkinson's diseaseGARCIA-REITBÖCK, Pablo; ANICHTCHIK, Oleg; GOEDERT, Michel et al.Brain. 2010, Vol 133, pp 2032-2044, issn 0006-8950, 13 p., 7Article

Biochemical characterization of a neuroserpin variant associated with hereditary dementiaYAZAKI, Masahide; LIEPNIEKS, Juris J; MURRELL, Jill R et al.The American journal of pathology. 2001, Vol 158, Num 1, pp 227-233, issn 0002-9440Article

Association of Ideomotor Apraxia With Frontal Gray Matter Volume Loss in Corticobasal SyndromeHUEY, Edward D; PARDINI, Matteo; CAVANAGH, Alyson et al.Archives of neurology (Chicago). 2009, Vol 66, Num 10, pp 1274-1280, issn 0003-9942, 7 p.Article

Corticobasal syndrome associated with the A9D Progranulin mutationSPINA, Salvatore; MURRELL, Jill R; HUEY, Edward D et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 10, pp 892-900, issn 0022-3069, 9 p.Article

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Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide geneBARBEITO, Ana G; GARRINGER, Holly J; BARAIBAR, Martin A et al.Journal of neurochemistry. 2009, Vol 109, Num 4, pp 1067-1078, issn 0022-3042, 12 p.Article

The tauopathy associated with mutation +3 in intron 10 of Tau : characterization of the MSTD familySPINA, Salvatore; FARLOW, Martin R; GHETTI, Bernardino et al.Brain. 2008, Vol 131, pp 72-89, issn 0006-8950, 18 p., 1Article

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Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutationBOEVE, Bradley F; TREMONT-LUKATS, Ivo W; KOPPIKAR, Vinaya et al.Brain. 2005, Vol 128, pp 752-772, issn 0006-8950, 21 p., 4Article