Alzheimer’s disease phenotypes and genotypes associated with mutations in presenilin 2

A Novel Italian Presenilin 2 Gene Mutation with Prevalent Behavioral Phenotype

(2017) Gabriella Marcon et al.   JOURNAL OF ALZHEIMERS DISEASE

Epilepsy and Cognitive Impairments in Alzheimer Disease

(2009) Jorge J. Palop   ARCHIVES OF NEUROLOGY

Seizures in Alzheimer Disease

(2009) Nikolaos Scarmeas et al.   ARCHIVES OF NEUROLOGY

Alterations in excitotoxicity and prostaglandin metabolism in a transgenic mouse model of Alzheimer's disease

(2009) Eva C. Schulte et al.   NEUROCHEMISTRY INTERNATIONAL

A Swedish family with de novo α-synuclein A53T mutation: Evidence for early cortical dysfunction

(2009) Andreas Puschmann et al.   PARKINSONISM & RELATED DISORDERS

RESEARCH ARTICLE: Empiric Refinement of the Pathologic Assessment of Lewy-Related Pathology in the Dementia Patient

(2008) James B. Leverenz et al.   BRAIN PATHOLOGY

A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment

(2008) S. G. Lindquist et al.   EUROPEAN JOURNAL OF NEUROLOGY

Intramembrane Proteolysis of GXGD-type Aspartyl Proteases Is Slowed by a Familial Alzheimer Disease-like Mutation

(2008) Regina Fluhrer et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism

(2008) L. Bernardi et al.   JOURNAL OF NEUROLOGY

A novel PSEN2 mutation associated with a peculiar phenotype

(2008) P. Piscopo et al.   NEUROLOGY

Defective signal transduction in B lymphocytes lacking presenilin proteins

(2008) T. Yagi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA