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Manic depressive illness in a founder population

European journal of human genetics : EJHG, 2003-08, Vol.11 (8), p.597-602

2003

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Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene

Brain (London, England : 1878), 1999-12, Vol.122 (12), p.2375-2386

1999

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The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid β-protein gene

Nature (London), 1987-09, Vol.329 (6135), p.156-157

1987

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Encephalopathie par implantation accidentelle d'aluminium metallique dans le cerveau humain. Etude combinee par microsonde et neuropahologie classique et ultrastructurale

Biology of the cell, 1988, Vol.63 (S1), p.26-26a

1988

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Absence of Duplication of Chromosome 21 Genes in Familial and Sporadic Alzheimer's Disease

Science (American Association for the Advancement of Science), 1987-10, Vol.238 (4827), p.664-666

1987

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Modifications of Oligodendroglial Cells in Spongiform Encephalopathies

Experimental neurology, 1998-11, Vol.154 (1), p.23-30

1998

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The Genetic Defect Causing Familial Alzheimer's Disease Maps on Chromosome 21

Science (American Association for the Advancement of Science), 1987-02, Vol.235 (4791), p.885-890

1987

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Relationship between non-fibrillary amyloid precursors and cell processes in the cortical neuropil of Alzheimer patients

Neuroscience letters, 1991-08, Vol.129 (1), p.119-122

1991

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Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation

Archives of neurology (Chicago), 2004-08, Vol.61 (8), p.1314

2004

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Supratentorial low-grade astrocytomas in adults

Neurosurgery, 1993-04, Vol.32 (4), p.554-559

1993

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Genotypic differences in hemangiopericytic meningioma

Human pathology, 1991-04, Vol.22 (4), p.402-402

1991

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Cerebral Edema Associated with Meningiomas: Possible Role of a Secretory-Excretory Phenomenon

Neurosurgery, 1984-01, Vol.14 (3), p.295-301

1984

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Widespread immunoreactivity of presenilin in neurons of normal and Alzheimer's disease brains : double-labeling immunohistochemical study

Acta neuropathologica, 1996-10, Vol.92 (4), p.325-330

1996

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Putative neurosurgical transmission of Creutzfeldt-Jakob disease with analysis of donor and recipient: agent strains

Comptes rendus de l'Académie des sciences, Série III, Sciences de la vie, 1997-04, Vol.320 (4), p.319-328

1997

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An Embedding Method for Monolayer Cell Cultures for Light and Electron Microscopy

Biotechnic & histochemistry, 1977-01, Vol.52 (4), p.240-242

1977

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Creutzfeldt-Jakob disease

The Lancet (British edition), 1996-05, Vol.347 (9011), p.1332-1333

1996

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Comparison of Clinical and Pathological Phenotypes in Two Ethnically and Geographically Unrelated Pedigrees Segregating an Equivalent Presenilin 1 Mutation

The journal of neuropsychiatry and clinical neurosciences, 2000, Vol.12 (3), p.359-363

2000

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Cerebral edema associated with meningiomas: possible role of a secretory-excretory phenomenon

Neurosurgery, 1984-03, Vol.14 (3), p.295-301

1984

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Mixed features of Alzheimer disease and Creutzfeldt-Jakob disease in a family with a presenilin 1 mutation in chromosome 14

Amyloid, 1996, Vol.3 (4), p.223-233

1996

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Detection of homozygosity by descent

European journal of human genetics : EJHG, 1995, Vol.3 (3), p.203-204

1995

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Senile plaques, "aging" and Alzheimer's disease

Acta neuropathologica, 1994-12, Vol.88 (6), p.600-601

1994

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Supratentorial Low-Grade Astrocytomas in Adults

Neurosurgery, 1993-04, Vol.32 (4), p.554-559

1993

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A New Italian Pedigree with Early-Onset Alzheimer's Disease

Journal of geriatric psychiatry and neurology, 1994-01, Vol.7 (1), p.28-32

1994

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Alzheimer's Disease: A Model From the Quantitative Study of a Large Kindred

Journal of geriatric psychiatry and neurology, 1992-07, Vol.5 (3), p.126-131

1992

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Primary and borderline brain lymphosarcoma: a neuropathological review of nine cases

Acta neuropathologica. Supplementum, 1975, Vol.Suppl 6, p.107

1975

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Manic depressive illness in a founder population

Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene

The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid β-protein gene

Encephalopathie par implantation accidentelle d'aluminium metallique dans le cerveau humain. Etude combinee par microsonde et neuropahologie classique et ultrastructurale

Absence of Duplication of Chromosome 21 Genes in Familial and Sporadic Alzheimer's Disease

Modifications of Oligodendroglial Cells in Spongiform Encephalopathies

The Genetic Defect Causing Familial Alzheimer's Disease Maps on Chromosome 21

Relationship between non-fibrillary amyloid precursors and cell processes in the cortical neuropil of Alzheimer patients

Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation

Supratentorial low-grade astrocytomas in adults

Genotypic differences in hemangiopericytic meningioma

Cerebral Edema Associated with Meningiomas: Possible Role of a Secretory-Excretory Phenomenon

Widespread immunoreactivity of presenilin in neurons of normal and Alzheimer's disease brains : double-labeling immunohistochemical study

Putative neurosurgical transmission of Creutzfeldt-Jakob disease with analysis of donor and recipient: agent strains

An Embedding Method for Monolayer Cell Cultures for Light and Electron Microscopy

Creutzfeldt-Jakob disease

Comparison of Clinical and Pathological Phenotypes in Two Ethnically and Geographically Unrelated Pedigrees Segregating an Equivalent Presenilin 1 Mutation

Cerebral edema associated with meningiomas: possible role of a secretory-excretory phenomenon

Mixed features of Alzheimer disease and Creutzfeldt-Jakob disease in a family with a presenilin 1 mutation in chromosome 14

Detection of homozygosity by descent

Senile plaques, "aging" and Alzheimer's disease

Supratentorial Low-Grade Astrocytomas in Adults

A New Italian Pedigree with Early-Onset Alzheimer's Disease

Alzheimer's Disease: A Model From the Quantitative Study of a Large Kindred

Primary and borderline brain lymphosarcoma: a neuropathological review of nine cases

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