Variant Alzheimer Disease With Spastic paraparesis: Neuropathological phenotype-Reference-Cited by-同舟云学术

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Variant Alzheimer Disease With Spastic paraparesis: Neuropathological phenotype

Published:2001-05 Issue:5 Volume:60 Page:483-492
ISSN:0022-3069
Container-title:Journal of Neuropathology & Experimental Neurology
language:en
Short-container-title:J Neuropathol Exp Neurol

Author:

Verkkoniemi Auli,Kalimo Hannu,Paetau Anders,Somer Mirja,Iwatsubo Takeshi,Hardy John,Haltia Matti

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine

Reference47 articles.

1. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

2. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

3. The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families

4. Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus

5. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

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3. Spastic Paraplegia and Cognitive Impairment Due to a De Novo Pathogenic Variant in Presenilin ‐1 ;Movement Disorders Clinical Practice;2022-10-23

4. Structural MRI Reveals Cervical Spinal Cord Atrophy in the P301L Mouse Model of Tauopathy: Gender and Transgene-Dosing Effects;Frontiers in Aging Neuroscience;2022-05-02

5. 11C-PiB PET can underestimate brain amyloid-β burden when cotton wool plaques are numerous;Brain;2021-12-16

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