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Should spinocerebellar ataxia type 5 be called Lincoln ataxia?NEE, L. E; HIGGINS, J. J.Neurology. 1997, Vol 49, Num 1, pp 298-302, issn 0028-3878Article

Alzheimer's disease in 22 twin pairs : 13-year follow-up : Hormonal, infectious and traumatic factorsNEE, L. E; LIPPA, C. F.Dementia and geriatric cognitive disorders. 1999, Vol 10, Num 2, pp 148-151, issn 1420-8008Article

Serum- and bradykinin-induced calcium transients in familial Alzheimer's fibroblastsMCCOY, K. R; MULLINS, R. D; NEWCOMB, T. G et al.Neurobiology of aging. 1993, Vol 14, Num 5, pp 447-455, issn 0197-4580Article

Alzheimer disease fibroblasts are hypersensitive to the lethal effects of a DNA-damaging chemicalSCUDIERO, D. A; POLINSKY, R. J; BRUMBACK, R. A et al.Mutation research. 1986, Vol 159, Num 1-2, pp 125-131, issn 0027-5107Article

Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer diseasePULST, S.-M; FAIN, P; COHN, V et al.Human genetics. 1991, Vol 87, Num 2, pp 159-161, issn 0340-6717Article

Hippocampal lesions in dominantly inherited Alzheimer's diseaseSTRUBLE, R. G; POLINSKY, R. J; HEDREEN, J. C et al.Journal of neuropathology and experimental neurology. 1991, Vol 50, Num 1, pp 82-94, issn 0022-3069Article

HLA in autonomic failureNEE, L. E; BROWN, R. T; POLINSKY, R. J et al.Archives of neurology (Chicago). 1989, Vol 46, Num 7, pp 758-759, issn 0003-9942Article

An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegiaHIGGINS, J. J; LOVELESS, J. M; GOSWAMI, S et al.Neurology. 2001, Vol 56, Num 11, pp 1482-1485, issn 0028-3878Article

Familial Alzheimer's disease: Site of mutation influences clinical phenotypeLIPPA, C. F; SWEARER, J. M; KANE, K. J et al.Annals of neurology. 2000, Vol 48, Num 3, pp 376-379, issn 0364-5134Article

Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees : effects of marker allele frequencies on lod scoresNECHIPORUK, A; FAIN, P; KORT, E et al.American journal of medical genetics. 1993, Vol 48, Num 1, pp 63-66, issn 0148-7299Article

Dominantly inherited Alzheimer's disease: cerebral glucose metabolismPOLINSKY, R. J; NOBLE, H; DI CHIRO, G et al.Journal of neurology, neurosurgery and psychiatry. 1987, Vol 50, Num 6, pp 752-757, issn 0022-3050Article

Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutationLIPPA, Carol F; ZHUKAREVA, Victoria; LEE, Virginia M.-Y et al.Annals of neurology. 2000, Vol 48, Num 6, pp 850-858, issn 0364-5134Article

A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degenerationHIGGINS, J. J; LITVAN, I; NEE, L. E et al.Neurology. 1999, Vol 52, Num 2, pp 404-406, issn 0028-3878Article

Decreased DNA repair in familial Alzheimer's diseaseJONES, S. K; NEE, L. E; SWEET, L et al.Mutation research. 1989, Vol 219, Num 4, pp 247-255, issn 0027-5107Article

Hypersensitivity to DNA-damaging agents in cultured cells from patients with Usher's syndrome and Duchenne muscular dystrophyROBBINS, J. H; SCUDIERO, D. A; GANGES, M. B et al.Journal of neurology, neurosurgery and psychiatry. 1984, Vol 47, Num 4, pp 391-398, issn 0022-3050Article

Amyloid-β-protein isoforms in brain of subjects with PS1-linked, βAPP-linked and sporadic alzheimer diseaseTAMAOKA, A; FRASER, P. E; YU, G et al.Molecular brain research. 1998, Vol 56, Num 1-2, pp 178-185, issn 0169-328XArticle

A gene (ETM) for essential tremor maps to chromosome 2p22-p25HIGGINS, J. J; PHO, L. T; NEE, L. E et al.Movement disorders. 1997, Vol 12, Num 6, pp 859-864, issn 0885-3185Article

An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosaHIGGINS, J. J; MORTON, D. H; PATRONAS, N et al.Neurology. 1997, Vol 49, Num 6, pp 1717-1720, issn 0028-3878Article

Mutations in American families with spinocerebellar ataxia (SCA) type 3 : SCA3 is allelic to Machado-Joseph diseaseHIGGINS, J. J; NEE, L. E; VASCONCELOS, O et al.Neurology. 1996, Vol 46, Num 1, pp 208-213, issn 0028-3878Article

Studies of activated microglial cells and macrophages using Alzheimer's disease cerebrospinal fluid in adult rats with experimentally induced lesionsLING, E. A; DAHLSTRÖM, A; POLINSKY, R. J et al.Neuroscience. 1992, Vol 51, Num 4, pp 815-825, issn 0306-4522Article

Familial Alzheimer disease: a large, multigeneration German kindredFROMMELT, P; SCHNABEL, R; KÜHNE, W et al.Alzheimer disease and associated disorders. 1991, Vol 5, Num 1, pp 36-43, issn 0893-0341, 8 p.Article

Parkinson's disease and Alzheimer's disease: hypersensitivity to X rays in cultured cell linesROBBINS, J. H; OTSUKA, F; TARONE, R. E et al.Journal of neurology, neurosurgery and psychiatry. 1985, Vol 48, Num 9, pp 916-923, issn 0022-3050Article

AMY plaques in familial AD : Comparison with sporadic Alzheimer's diseaseLIPPA, C. F; SCHMIDT, M. L; NEE, L. E et al.Neurology. 2000, Vol 54, Num 1, pp 100-104, issn 0028-3878Article

-42 deposition precedes other changes in PS-1 Alzheimer's diseaseLIPPA, C. F; NEE, L. E; MORI, H et al.Lancet (British edition). 1998, Vol 352, Num 9134, pp 1117-1118, issn 0140-6736Article

Progressive supranuclear gaze palsy is in linkage disequilibrium with the τ and not the α-synuclein geneHIGGINS, J. J; LITVAN, I; PHO, L. T et al.Neurology. 1998, Vol 50, Num 1, pp 270-273, issn 0028-3878Article

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