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Titolo:
FRONTOTEMPORAL DEMENTIA AND PARKINSONISM LINKED TO CHROMOSOME-17 - A CONSENSUS CONFERENCE
Autore:
FOSTER NL; WILHELMSEN K; SIMA AAF; JONES MZ; DAMATO CJ; GILMAN S; SPILLANTINI MG; LYNCH T; MAYEUX RP; GASKELL PC; HULETTE CM; PERICAKVANCE MA; WELSHBOHMER KA; DICKSON DW; HEUTINK P; KROS J; VANSWIETEN JC; ARWERT F; GHETTI MB; MURRELL J; LANNFELT L; HUTTON M; JONES M; PHELPS CH; SNYDER DS; OLIVER E; BALL MJ; CUMMINGS JL; MILLER BL; KATZMAN R; REED L; SCHELPER RL; LANDSKA DJ; BRUN A; FINK JK; KUHL DE; KNOPMAN DS; WSZOLEK Z; MILLER CA; BIRD TD; LENDON C; ELECHI C;
Indirizzi:
UNIV MICHIGAN,MED CTR,TAUBMAN CTR 1920,DEPT NEUROL,BOX 0316 ANN ARBORMI 48109 UNIV MICHIGAN,DEPT PATHOL ANN ARBOR MI 48109 WAYNE STATE UNIV,DEPT PATHOL DETROIT MI 48202 WAYNE STATE UNIV,DEPT NEUROL DETROIT MI 48202 MICHIGAN STATE UNIV,DEPT PATHOL E LANSING MI 48824 UNIV CALIF SAN FRANCISCO,DEPT NEUROL SAN FRANCISCO CA 94143
Titolo Testata:
Annals of neurology
fascicolo: 6, volume: 41, anno: 1997,
pagine: 706 - 715
SICI:
0364-5134(1997)41:6<706:FDAPLT>2.0.ZU;2-5
Fonte:
ISI
Lingua:
ENG
Soggetto:
AUTOSOMAL-DOMINANT PARKINSONISM; PROGRESSIVE SUBCORTICAL GLIOSIS; FRONTAL-LOBE DEGENERATION; PONTO-NIGRAL DEGENERATION; NON-ALZHEIMER TYPE; NEUROFIBRILLARY TANGLES; SUPRANUCLEAR PALSY; FAMILIAL DEMENTIA; PICKS-DISEASE; NEUROPATHOLOGY;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Science Citation Index Expanded
Citazioni:
41
Recensione:
Indirizzi per estratti:
Citazione:
N.L. Foster et al., "FRONTOTEMPORAL DEMENTIA AND PARKINSONISM LINKED TO CHROMOSOME-17 - A CONSENSUS CONFERENCE", Annals of neurology, 41(6), 1997, pp. 706-715

Abstract

We held an international consensus conference on frontotemporal dementia, behavioral disturbances, and parkinsonism linked to chromosome 17to determine whether these are homogeneous or heterogeneous disorders, to agree on terminology, and to develop strategies for further research. The group identified 13 kindreds with sufficient evidence for linkage, finding in common to all a critical 2 cM between markers D17S791and D17S800. There was agreement that (1) despite previous descriptions that have emphasized one or another clinical or neuropathological feature, the kindreds share clinical and neuropathological features; (2) until more specific information about the genetic defects becomes available, this disorder is best termed frontotemporal dementia and parkinsonism linked to chromosome 17; and (3) further research will be enhanced by identifying the gene or genes responsible for this disorder, detecting additional cases within known families and, in new families,correlating mutations with phenotypes and more fully delineating the clinical, neuropsychological, and neuropathological characteristics ofthis disorder.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 08/07/20 alle ore 06:28:40