Progressive dementia and leucoencephalopathy as the initial presentation of late onset hereditary cystatin-C amyloidosis Clinicopathological presentation of two cases

Author:

Sveinbjörnsdóttir Sigurlaug,Blöndal Hannes,Gudmundsson Gretar,Kjartansson Ólafur,Jónsdóttir Sif,Gudmundsson Gunnar

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference33 articles.

1. Hereditary cystatin C amyloid angiopathy: identificatin of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis;Abrahamson;Hum. Genet.,1992

2. Cerebral amyloid angiopathy presenting as multiple intracranial lesions on magnetic resonance imaging;Awasthi;J. Neurosurg.,1991

3. Cystein proteinase inhibitors of the cystatin superfamily;Barrett,1986

4. Dementia with non-hereditary cystatin-C angiopathy;Benedikz;Alzheimer's Dis. Relat. Dis.,1989

5. Hereditary cystatin C amyloidosis: The Icelandic type. Investigation of an asymptomatic individual;Benedikz;J. Trop. Geogr. Neurol.,1991

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