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3. Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21. Wijker M; Wszolek ZK; Wolters EC; Rooimans MA; Pals G; Pfeiffer RF; Lynch T; Rodnitzky RL; Wilhelmsen KC; Arwert F Hum Mol Genet; 1996 Jan; 5(1):151-4. PubMed ID: 8789453 [TBL] [Abstract][Full Text] [Related]
4. Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. Lynch T; Sano M; Marder KS; Bell KL; Foster NL; Defendini RF; Sima AA; Keohane C; Nygaard TG; Fahn S Neurology; 1994 Oct; 44(10):1878-84. PubMed ID: 7936241 [TBL] [Abstract][Full Text] [Related]
5. Rapidly progressive autosomal dominant Parkinsonism and dementia with Pallido-Ponto-Nigral Gegeneration (PPND) and Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex (DDPAC) are clinically distinct conditions that are both linked to 17q21-22. Wszolek ZK; Lynch T; Wilhelmsen KC Parkinsonism Relat Disord; 1997 Apr; 3(2):67-76. PubMed ID: 18591058 [TBL] [Abstract][Full Text] [Related]
6. Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22. Baker M; Kwok JB; Kucera S; Crook R; Farrer M; Houlden H; Isaacs A; Lincoln S; Onstead L; Hardy J; Wittenberg L; Dodd P; Webb S; Hayward N; Tannenberg T; Andreadis A; Hallupp M; Schofield P; Dark F; Hutton M Ann Neurol; 1997 Nov; 42(5):794-8. PubMed ID: 9392579 [TBL] [Abstract][Full Text] [Related]
7. Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism. Hardy J; Pérez-Tur J; Baker M; Farrer M; Crook R; Hutton M; Johnson WG; Gwinn K; Muenter M; Rocca WA; Maraganore D Am J Med Genet; 1998 Mar; 81(2):166-71. PubMed ID: 9613857 [TBL] [Abstract][Full Text] [Related]
8. Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21. Froelich S; Basun H; Forsell C; Lilius L; Axelman K; Andreadis A; Lannfelt L Am J Med Genet; 1997 Jul; 74(4):380-5. PubMed ID: 9259373 [TBL] [Abstract][Full Text] [Related]
15. Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval. Rademakers R; Cruts M; Dermaut B; Sleegers K; Rosso SM; Van den Broeck M; Backhovens H; van Swieten J; van Duijn CM; Van Broeckhoven C Mol Psychiatry; 2002; 7(10):1064-74. PubMed ID: 12476321 [TBL] [Abstract][Full Text] [Related]
16. Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684. Hulette CM; Pericak-Vance MA; Roses AD; Schmechel DE; Yamaoka LH; Gaskell PC; Welsh-Bohmer KA; Crowther RA; Spillantini MG J Neuropathol Exp Neurol; 1999 Aug; 58(8):859-66. PubMed ID: 10446810 [TBL] [Abstract][Full Text] [Related]
17. Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants. Foster NL; Wilhelmsen K; Sima AA; Jones MZ; D'Amato CJ; Gilman S Ann Neurol; 1997 Jun; 41(6):706-15. PubMed ID: 9189031 [TBL] [Abstract][Full Text] [Related]
18. Determination of the gene structure of human GFAP and absence of coding region mutations associated with frontotemporal dementia with parkinsonism linked to chromosome 17. Isaacs A; Baker M; Wavrant-De Vrièze F; Hutton M Genomics; 1998 Jul; 51(1):152-4. PubMed ID: 9693047 [No Abstract] [Full Text] [Related]
19. Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22. Krakow D; Reinker K; Powell B; Cantor R; Priore MA; Garber A; Lachman RS; Rimoin DL; Cohn DH Am J Hum Genet; 1998 Jul; 63(1):120-4. PubMed ID: 9634519 [TBL] [Abstract][Full Text] [Related]
20. Tau is a candidate gene for chromosome 17 frontotemporal dementia. Poorkaj P; Bird TD; Wijsman E; Nemens E; Garruto RM; Anderson L; Andreadis A; Wiederholt WC; Raskind M; Schellenberg GD Ann Neurol; 1998 Jun; 43(6):815-25. PubMed ID: 9629852 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]