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A gene (ETM) for essential tremor maps to chromosome 2p22-p25

Movement disorders, 1997-11, Vol.12 (6), p.859-864

1997

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Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation

Annals of neurology, 2000-12, Vol.48 (6), p.850-858

2000

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Progressive supranuclear gaze palsy is in linkage disequilibrium with the tau and not the alpha-synuclein gene

Neurology, 1998-01, Vol.50 (1), p.270

1998

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Familial Alzheimer's disease: Site of mutation influences clinical phenotype

Annals of neurology, 2000-09, Vol.48 (3), p.376-379

2000

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Lewy Bodies Contain Altered α-Synuclein in Brains of Many Familial Alzheimer's Disease Patients with Mutations in Presenilin and Amyloid Precursor Protein Genes

The American journal of pathology, 1998-11, Vol.153 (5), p.1365-1370

1998

Volltextzugriff (PDF)

Presenilin 1 Suppresses the Function of c-Jun Homodimers via Interaction with QM/Jif-1

The Journal of cell biology, 1999-10, Vol.147 (1), p.121-133

1999

Volltextzugriff (PDF)

Aβ −42 deposition precedes other changes in PS-1 Alzheimer's disease

The Lancet (British edition), 1998-10, Vol.352 (9134), p.1117-1118

1998

Volltextzugriff (PDF)

Alzheimer's disease in 22 twin pairs--13-year follow-up: hormonal, infectious and traumatic factors

Dementia and geriatric cognitive disorders, 1999-03, Vol.10 (2), p.148

1999

Volltextzugriff (PDF)

An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia

Neurology, 2001-06, Vol.56 (11), p.1482

2001

Volltextzugriff (PDF)

Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease

Neurology, 1996-01, Vol.46 (1), p.208

1996

Volltextzugriff (PDF)

Fluorescent Light-Induced Chromatid Breaks Distinguish Alzheimer Disease Cells from Normal Cells in Tissue Culture

Proceedings of the National Academy of Sciences - PNAS, 1996-05, Vol.93 (10), p.5146-5150

1996

Volltextzugriff (PDF)

An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosa

Neurology, 1997-12, Vol.49 (6), p.1717

1997

Volltextzugriff (PDF)

Dementia of the Alzheimer type: clinical and family study of 22 twin pairs

Neurology, 1987-03, Vol.37 (3), p.359

1987

Volltextzugriff (PDF)

Evidence for a new spinocerebellar ataxia locus

Movement disorders, 1997-05, Vol.12 (3), p.412-417

1997

Volltextzugriff (PDF)

A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration

Neurology, 1999-01, Vol.52 (2), p.404

1999

Volltextzugriff (PDF)

Serum- and bradykinin-induced calcium transients in familial Alzheimer's fibroblasts

Neurobiology of aging, 1993-09, Vol.14 (5), p.447-455

1993

Volltextzugriff (PDF)

Should spinocerebellar ataxia type 5 be called Lincoln ataxia?

Neurology, 1997-07, Vol.49 (1), p.298

1997

Volltextzugriff (PDF)

Brain MRI, lumbar CSF monoamine concentrations, and clinical descriptors of patients with spinocerebellar ataxia mutations

Journal of neurology, neurosurgery and psychiatry, 1996-12, Vol.61 (6), p.591-595

1996

Volltextzugriff (PDF)

Studies of activated microglial cells and macrophages using Alzheimer's disease cerebrospinal fluid in adult rats with experimentally induced lesions

Neuroscience, 1992-12, Vol.51 (4), p.815-825

1992

Volltextzugriff (PDF)

Familial Alzheimer disease: a large, multigeneration German kindred

Alzheimer disease and associated disorders, 1991, Vol.5 (1), p.36-43

1991

Volltextzugriff (PDF)

Amyloid- β-protein isoforms in brain of subjects with PS1-linked, βAPP-linked and sporadic Alzheimer disease

Brain research. Molecular brain research., 1998-05, Vol.56 (1), p.178-185

1998

Volltextzugriff (PDF)

Dominantly inherited Alzheimer's disease: cerebral glucose metabolism

Journal of neurology, neurosurgery and psychiatry, 1987-06, Vol.50 (6), p.752-757

1987

Volltextzugriff (PDF)

Parkinson's disease and Alzheimer's disease: hypersensitivity to X rays in cultured cell lines

Journal of neurology, neurosurgery and psychiatry, 1985-09, Vol.48 (9), p.916-923

1985

Volltextzugriff (PDF)

Hippocampal Lesions in Dominantly Inherited Alzheimerʼs Disease

Journal of neuropathology and experimental neurology, 1991-01, Vol.50 (1), p.82-94

1991

Volltextzugriff (PDF)

Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer disease

Human genetics, 1991-06, Vol.87 (2), p.159-161

1991

Volltextzugriff (PDF)

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A gene (ETM) for essential tremor maps to chromosome 2p22-p25

Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation

Progressive supranuclear gaze palsy is in linkage disequilibrium with the tau and not the alpha-synuclein gene

Familial Alzheimer's disease: Site of mutation influences clinical phenotype

Lewy Bodies Contain Altered α-Synuclein in Brains of Many Familial Alzheimer's Disease Patients with Mutations in Presenilin and Amyloid Precursor Protein Genes

Presenilin 1 Suppresses the Function of c-Jun Homodimers via Interaction with QM/Jif-1

Aβ −42 deposition precedes other changes in PS-1 Alzheimer's disease

Alzheimer's disease in 22 twin pairs--13-year follow-up: hormonal, infectious and traumatic factors

An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia

Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease

Fluorescent Light-Induced Chromatid Breaks Distinguish Alzheimer Disease Cells from Normal Cells in Tissue Culture

An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosa

Dementia of the Alzheimer type: clinical and family study of 22 twin pairs

Evidence for a new spinocerebellar ataxia locus

A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration

Serum- and bradykinin-induced calcium transients in familial Alzheimer's fibroblasts

Should spinocerebellar ataxia type 5 be called Lincoln ataxia?

Brain MRI, lumbar CSF monoamine concentrations, and clinical descriptors of patients with spinocerebellar ataxia mutations

Studies of activated microglial cells and macrophages using Alzheimer's disease cerebrospinal fluid in adult rats with experimentally induced lesions

Familial Alzheimer disease: a large, multigeneration German kindred

Amyloid- β-protein isoforms in brain of subjects with PS1-linked, βAPP-linked and sporadic Alzheimer disease

Dominantly inherited Alzheimer's disease: cerebral glucose metabolism

Parkinson's disease and Alzheimer's disease: hypersensitivity to X rays in cultured cell lines

Hippocampal Lesions in Dominantly Inherited Alzheimerʼs Disease

Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer disease

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