(Q34220982)

31 July 2017

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title

The Worster-Drought syndrome and other syndromes of dementia with spastic paraparesis: the paradox of molecular pathology (English)

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31 July 2017

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Worster-Drought syndrome

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Masters CL

1

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31 July 2017

Beyreuther K

series ordinal

2

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31 July 2017

language of work or name

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1 April 2001

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Journal of Neuropathology & Experimental Neurology

31 July 2017

published in

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31 July 2017

volume

60

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31 July 2017

issue

4

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31 July 2017

page(s)

317-319

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Familial Presenile Dementia with Spastic Paralysis

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

A decamer duplication in the 3' region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

Novel prion protein gene mutation in an octogenarian with Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

Variable phenotype of Alzheimer's disease with spastic paraparesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

Clearance of Alzheimer's amyloid-ss(1-40) peptide from brain by LDL receptor-related protein-1 at the blood-brain barrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.317

21 January 2018

Identifiers

DOI

10.1093/JNEN/60.4.317

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31 July 2017

1 reference