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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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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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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

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Should spinocerebellar ataxia type 5 be called Lincoln ataxia?

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

1997

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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)

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)

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)

Proteolytic processing of presenilin-1 (PS-1) is not associated with Alzheimer's disease with or without PS-1 mutations

FEBS letters, 1997-11, Vol.418 (1), p.162-166

1997

Volltextzugriff (PDF)

Platelet APP isoform ratios in asymptomatic young adults expressing an AD-related presenilin-1 mutation

Journal of the neurological sciences, 2001-01, Vol.183 (1), p.85-88

2001

Volltextzugriff (PDF)

TNF-α and IL-1β–mediated regulation of MMP-9 and TIMP-1 in renal proximal tubular cells

Kidney international, 2004-10, Vol.66 (4), p.1376-1386

2004

Volltextzugriff (PDF)

Prothrombotic factors in children with stroke or porencephaly

Pediatrics (Evanston), 2005-08, Vol.116 (2), p.447

2005

Volltextzugriff (PDF)

Effects of Psychosocial Interactions at a Cellular Level

Social work (New York), 1995-03, Vol.40 (2), p.259-262

Nee, Linda E.

1995

Volltextzugriff (PDF)

Linkage of familial alzheimer disease to chromosome 14 in two large early-onset pedigrees: Effects of marker allele frequencies on lod scores

American journal of medical genetics, 1993-05, Vol.48 (1), p.63-66

1993

Volltextzugriff (PDF)

Asyndromic Bilateral Transverse Facial Cleft

Annals of medical and health sciences research, 2013-01, Vol.3 (1), p.122-124

2013

Volltextzugriff (PDF)

Radiosensitivity in alzheimer disease and Parkinson disease

The Lancet (British edition), 1983-02, Vol.1 (8322), p.468-469

1983

Volltextzugriff (PDF)

(A Beta-42) deposition precedes other changes in PS-1 Alzheimer's disease

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

1998

Volltextzugriff (PDF)

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

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

1998

Volltextzugriff (PDF)

DNA repair deficiency for alkylation damage in cells from Alzheimer's disease patients

Progress in clinical and biological research, 1989, Vol.317, p.715

1989

Volltextzugriff (PDF)

Frontotemporal dementia with novel tau pathology and a Glu342Valtau mutation

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

2000

Volltextzugriff (PDF)

Clinical research in neuropsychiatry

General hospital psychiatry, 1983-01, Vol.5 (2), p.105-109

1983

Volltextzugriff (PDF)

Alzheimer's Disease: Headlines, Confusion, and the Unknown

Journal of geriatric psychiatry and neurology, 1993-04, Vol.6 (2), p.65-65

Nee, Linda E.

1993

Volltextzugriff (PDF)

Asyndromic bilateral transverse facial cleft

Annals of medical and health sciences research, 2013, Vol.3 (1), p.122-124

2013

Volltextzugriff (PDF)

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

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

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

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

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

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

Proteolytic processing of presenilin-1 (PS-1) is not associated with Alzheimer's disease with or without PS-1 mutations

Platelet APP isoform ratios in asymptomatic young adults expressing an AD-related presenilin-1 mutation

TNF-α and IL-1β–mediated regulation of MMP-9 and TIMP-1 in renal proximal tubular cells

Prothrombotic factors in children with stroke or porencephaly

Effects of Psychosocial Interactions at a Cellular Level

Linkage of familial alzheimer disease to chromosome 14 in two large early-onset pedigrees: Effects of marker allele frequencies on lod scores

Asyndromic Bilateral Transverse Facial Cleft

Radiosensitivity in alzheimer disease and Parkinson disease

(A Beta-42) deposition precedes other changes in PS-1 Alzheimer's disease

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

DNA repair deficiency for alkylation damage in cells from Alzheimer's disease patients

Frontotemporal dementia with novel tau pathology and a Glu342Valtau mutation

Clinical research in neuropsychiatry

Alzheimer's Disease: Headlines, Confusion, and the Unknown

Asyndromic bilateral transverse facial cleft

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