Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 94

1.

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.

2.
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.

PMID:
8789453
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, et al.

Neurology. 1994 Oct;44(10):1878-84.

PMID:
7936241
5.

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
6.

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 28;81(2):166-71.

PMID:
9613857
7.

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
8.

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
10.

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.

11.

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994.

Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, Sima AA, Keohane C, Nygaard TG, Fahn S, Mayeux R, Rowland LP, Wilhelmsen KC.

Neurology. 2001 Nov;57(10 Suppl 3):S39-45. No abstract available.

PMID:
11775599
12.

Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22.

Mangino M, Sanchez O, Torrente I, De Luca A, Capon F, Novelli G, Dallapiccola B.

Am J Hum Genet. 1999 Aug;65(2):441-7.

13.

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
14.

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
15.

The NIK protein kinase and C17orf1 genes: chromosomal mapping, gene structures and mutational screening in frontotemporal dementia and parkinsonism linked to chromosome 17.

Aronsson FC, Magnusson P, Andersson B, Karsten SL, Shibasaki Y, Lendon CL, Goate AM, Brookes AJ.

Hum Genet. 1998 Sep;103(3):340-5.

PMID:
9799091
16.

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
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. Review.

18.

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
19.

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
20.

Tau and neurofilaments in a family with frontotemporal dementia unlinked to chromosome 17q21-22.

Savioz A, Riederer BM, Heutink P, Rizzu P, Tolnay M, Kövari E, Probst A, Riederer Ir, Bouras C, Leuba G.

Neurobiol Dis. 2003 Feb;12(1):46-55.

PMID:
12609488

Supplemental Content

Support Center