Familial primary progressive aphasia

Alzheimer Disease and Associated Disorders

Volumn 17, Issue 2, 2003, Pages 106-112

  Krefft, Thomas A ^a   Graff Radford, Neill R ^a   Dickson, Dennis W ^a   Baker, Matt ^a   Castellani, Rudy J ^b  

^a MAYO CLINIC   (United States)

^b CASE WESTERN RESERVE UNIVERSITY   (United States)

Author keywords

Clinical; Hereditary; Pathology; Progressive aphasia

Indexed keywords

UBIQUITIN;

ADULT; AGED; ANOMIA; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BEHAVIOR DISORDER; CASE REPORT; CHROMOSOME 17; CHROMOSOME MUTATION; CLINICAL FEATURE; CONTROLLED STUDY; DEGENERATIVE DISEASE; DNA DETERMINATION; EXON; FAMILIAL DISEASE; FAMILY HISTORY; FEMALE; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; HUMAN TISSUE; LANGUAGE DISABILITY; MALE; MEMORY DISORDER; MOTOR DYSFUNCTION; ONSET AGE; PATHOLOGY; PRIMARY PROGRESSIVE APHASIA; PRIORITY JOURNAL;

AGE OF ONSET; AGED; APHASIA, PRIMARY PROGRESSIVE; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; PEDIGREE;

EID: 0037971512     PISSN: 08930341     EISSN: None     Source Type: Journal    
DOI: 10.1097/00002093-200304000-00009     Document Type: Article

References (17)

1. Basun H, Almkvist O, Axelman K, et al. Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia. Arch Neurol 1997;54:539-44.
2. Bird TD, Wijsrnan EM, Nochlin D, et al. Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD. Neurology 1997;48:949-54.
3. Ghorayeb I, Series C, Parchi P, et al. Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case. Neurology 1998;51:271-4.
4. Ikeda K, Akiyama H, Iritani S, et al. Corticobasal degeneration with primary progressive aphasia and accentuated cortical lesion in superior temporal gyrus: case report and review. Acta Neuropathol (Berl) 1996;92:534-9.
5. Kirshner HS, Tanridag O, Thurman L, et al. Progressive aphasia without dementia: two cases with focal spongiform degeneration. Ann Neurol 1987;22:527-32.
6. Knopman DS, Mastri AR, Frey WH 2nd, et al. Dementia lacking distinctive histologic features: a common non-Alzheimer degenerative dementia. Neurology 1990;40:251-6.
7. Lendon CL, Lynch T, Norton J, et al. Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22. Neurology 1998;50:1546-55.
8. Mandell AM, Alexander MP, Carpenter S. Creutzfeldt-Jakob disease presenting as isolated aphasia. Neurology 1989;39:55-8.
9. Mendez MF, Zander BA. Dementia presenting with aphasia: clinical characteristics. J Neurol Neurosurg Psychiatry 1991;54:542-5.
10. Mesulam MM. Slowly progressive aphasia without generalized dementia. Ann Neurol 1982;11:592-8.
11. Mesulam MM. Primary progressive aphasia. Ann Neurol 2001;49:425-32.
12. Morris JC, Cole M, Banker BQ, et al. Hereditary dysphasic dementia and the Pick-Alzheimer spectrum. Ann Neurol 1984;16:455-66.
13. Murrell JR, Spillantini MG, Zolo P, et al. Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits. J Neuropathol Exp Neurol 1999;58:1207-26.
14. Neary D, Snowden JS, Mann DM. The clinical pathological correlates of lobar atrophy. Dementia 1993;4:154-9.
15. Parchi P, Castellani R, Capellari S, et al. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 1996;39:767-78.
16. Snowden JS, Mann DMA, Neary D. Fronto-temporal Lobar Degeneration: Fronto-temporal Dementia, Progressive Aphasia, Semantic Dementia. New York: Churchill Livingstone, 1996
17. Weintraub S, Rubin NP, Mesulam MM. Primary progressive aphasia: longitudinal course, neuropsychological profile, and language features. Arch Neurol 1990;47:1329-35.