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Items: 1 to 20 of 102

1.

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.

PMID:
9392579
2.

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. Erratum in: Ann Neurol 1998 Sep;44(3):428.

PMID:
9629852
3.

Extended investigation of tau and mutation screening of other candidate genes on chromosome 17q21 in a Swedish FTDP-17 family.

Froelich Fabre S, Axelman P, Almkvist A, Basun H, Lannfelt L.

Am J Med Genet B Neuropsychiatr Genet. 2003 Aug 15;121B(1):112-8.

PMID:
12898585
4.

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.

Dumanchin C, Camuzat A, Campion D, Verpillat P, Hannequin D, Dubois B, Saugier-Veber P, Martin C, Penet C, Charbonnier F, Agid Y, Frebourg T, Brice A.

Hum Mol Genet. 1998 Oct;7(11):1825-9.

PMID:
9736786
5.

From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.

Nasreddine ZS, Loginov M, Clark LN, Lamarche J, Miller BL, Lamontagne A, Zhukareva V, Lee VM, Wilhelmsen KC, Geschwind DH.

Ann Neurol. 1999 Jun;45(6):704-15.

PMID:
10360762
6.

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.

PMID:
10446810
7.

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

Lendon CL, Lynch T, Norton J, McKeel DW Jr, Busfield F, Craddock N, Chakraverty S, Gopalakrishnan G, Shears SD, Grimmett W, Wilhelmsen KC, Hansen L, Morris JC, Goate AM.

Neurology. 1998 Jun;50(6):1546-55.

PMID:
9633693
8.

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.

9.

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.

PMID:
8789453
10.

Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families.

Heutink P, Stevens M, Rizzu P, Bakker E, Kros JM, Tibben A, Niermeijer MF, van Duijn CM, Oostra BA, van Swieten JC.

Ann Neurol. 1997 Feb;41(2):150-9.

PMID:
9029063
11.

Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia.

Basun H, Almkvist O, Axelman K, Brun A, Campbell TA, Collinge J, Forsell C, Froelich S, Wahlund LO, Wetterberg L, Lannfelt L.

Arch Neurol. 1997 May;54(5):539-44.

PMID:
9152110
12.

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 25;74(4):380-5.

PMID:
9259373
13.

Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.

Wilhelmsen KC, Lynch T, Pavlou E, Higgins M, Nygaard TG.

Am J Hum Genet. 1994 Dec;55(6):1159-65.

14.
15.

Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy.

Filla A, De Michele G, Cocozza S, Patrignani A, Volpe G, Castaldo I, Ruggiero G, Bonavita V, Masters C, Casari G, Bruni A.

Neurology. 2002 Mar 26;58(6):922-8.

PMID:
11914409
16.

Tau pathology in a family with dementia and a P301L mutation in tau.

Mirra SS, Murrell JR, Gearing M, Spillantini MG, Goedert M, Crowther RA, Levey AI, Jones R, Green J, Shoffner JM, Wainer BH, Schmidt ML, Trojanowski JQ, Ghetti B.

J Neuropathol Exp Neurol. 1999 Apr;58(4):335-45.

PMID:
10218629
17.

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.

Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, Rademakers R, Vandenberghe R, Dermaut B, Martin JJ, van Duijn C, Peeters K, Sciot R, Santens P, De Pooter T, Mattheijssens M, Van den Broeck M, Cuijt I, Vennekens K, De Deyn PP, Kumar-Singh S, Van Broeckhoven C.

Nature. 2006 Aug 24;442(7105):920-4. Epub 2006 Jul 16.

PMID:
16862115
18.

[Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP 17)].

Nakano I.

Ryoikibetsu Shokogun Shirizu. 1999;(27 Pt 2):20-3. Review. Japanese. No abstract available.

PMID:
10434580
19.

Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies.

Spillantini MG, Bird TD, Ghetti B.

Brain Pathol. 1998 Apr;8(2):387-402. Review.

PMID:
9546295

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