(Q53236678)

English

Atypical dementia and spastic paraplegia in a patient with primary lateral sclerosis and numerous necortical beta amyloid plaques: new disorder or Alzheimer's disease variant?

scientific article published in January 2000

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

Atypical dementia and spastic paraplegia in a patient with primary lateral sclerosis and numerous necortical beta amyloid plaques: new disorder or Alzheimer's disease variant? (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

0 references

Alzheimer's disease

1 reference

based on heuristic

inferred from title

author name string

P A Engel

1

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

M Grunnet

2

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

publication date

1 January 2000

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

Journal of Geriatric Psychiatry and Neurology

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

13

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

2

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

60-64

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families.

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q.

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15.

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Strümpell's familial spastic paraplegia: genetics and neuropathology

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

The neuropathology of hereditary spastic paraparesis

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Upper motor neuron predominant degeneration with frontal and temporal lobe atrophy

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Primary lateral sclerosis: a neuropsychological study.

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Cognitive impairment in families with pure autosomal dominant hereditary spastic paraparesis

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p.

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Congophilic angiopathy of the brain: a clinical and pathological report on two siblings

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1.

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Spastic tetraplegia as an initial manifestation of familial Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Comparison of two brief tests of organic brain impairment, the MSQ and the short portable MSQ.

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Application of the National Institute on Aging (NIA)-Reagan Institute criteria for the neuropathological diagnosis of Alzheimer disease.

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Neuropathological stageing of Alzheimer-related changes

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Distribution of Alzheimer-type pathologic changes in nondemented elderly individuals matches the pattern in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Association of late onset spastic paraparesis and dementia: probably an autosomal dominant form of complicated paraplegia

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Cytoskeletal pathology in familial cerebral amyloid angiopathy (British type) with non-neuritic amyloid plaque formation

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family

1 reference

https://api.crossref.org/works/10.1177%2F089198870001300203

21 January 2018

A stop-codon mutation in the BRI gene associated with familial British dementia

1 reference

https://opencitations.net/index/coci/api/v1/citations/10.1038/21637

15 July 2023

Identifiers

10.1177/089198870001300203

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/10912726

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q53236678&oldid=1934747721"