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Publications by Hannes O. Tiedt

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

Neurodegenerative Diseases

English

Related publications

Homozygosity of the Autosomal Dominant Alzheimer Disease Presenilin 1 E280A Mutation

English

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

Archives of Neurology

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

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

Canadian Journal of Neurological Sciences

English

Cortical Microstructural Correlates of Astrocytosis in Autosomal Dominant Alzheimer Disease

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

Variability of Age at Onset in Siblings With Familial Alzheimer Disease

Archives of Neurology

English

Abnormal Dark Adaptation Kinetics in Autosomal Dominant Sector Retinitis Pigmentosa Due to Rod Opsin Mutation.

British Journal of Ophthalmology

Molecular Neuroscience

Sensory Systems

English

Autosomal Dominant C1149R Von Willebrand Disease: Phenotypic Findings and Their Implications

English