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Publications by Bernadette Curry

Variant Alzheimer Disease With Spastic Paraparesis: A Rare Presenilin-1 Mutation

Canadian Journal of Neurological Sciences

English

Fatal Nemaline Myopathy in Infancy

Canadian Journal of Neurological Sciences

English

Related publications

Homozygosity of the Autosomal Dominant Alzheimer Disease Presenilin 1 E280A Mutation

English

Wide Range of Disease Onset in a Family With Alzheimer Disease and a His163Tyr Mutation in the Presenilin-1 Gene

Archives of Neurology

English

Alzheimer Disease: Presenilin Springs a Leak

Nature Medicine

Molecular Biology

English

Novel Presenilin 1 Mutation (S170F) Causing Alzheimer Disease With Lewy Bodies in the Third Decade of Life

Archives of Neurology

English

Phenotypic Variability in Autosomal Dominant Familial Alzheimer Disease Due to the S170F Mutation of Presenilin-1

Neurodegenerative Diseases

English

Formation of Tau Inclusions in Knock-In Mice With Familial Alzheimer Disease (FAD) Mutation of Presenilin 1 (PS1)

Journal of Biological Chemistry

Molecular Biology

English

Spastic Paraparesis, Cerebellar Ataxia, and Intention Tremor: A Severe Variant of FXTAS?

Journal of Medical Genetics

English

Mutation Analysis of the Spastin Gene (SPG4) in Patients With Hereditary Spastic Paraparesis

Journal of Medical Genetics

English

Microstructural Integrity of Cerebral Fiber Tracts in Hereditary Spastic Paraparesis With SPG11 Mutation

American Journal of Neuroradiology

Nuclear Medicine

English