BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 17995932)

  • 1. Variable phenotype of Alzheimer's disease with spastic paraparesis.
    Karlstrom H; Brooks WS; Kwok JB; Broe GA; Kril JJ; McCann H; Halliday GM; Schofield PR
    J Neurochem; 2008 Feb; 104(3):573-83. PubMed ID: 17995932
    [TBL] [Abstract][Full Text] [Related]  

  • 2. No association of spastic paraparesis genes in PSEN1 Alzheimer's disease with spastic paraparesis.
    Karlstrom H; Kwok JB; Gregory GC; Hallupp M; Brooks WS; Schofield PR
    Neuroreport; 2007 Aug; 18(12):1267-9. PubMed ID: 17632280
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A presenilin 1 mutation (Arg278Ser) associated with early onset Alzheimer's disease and spastic paraparesis.
    Raman A; Lin X; Suri M; Hewitt M; Constantinescu CS; Phillips MF
    J Neurol Sci; 2007 Sep; 260(1-2):78-82. PubMed ID: 17507029
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel presenilin 1 mutation (Y154N) in a patient with early onset Alzheimer's disease with spastic paraparesis.
    Hattori S; Sakuma K; Wakutani Y; Wada K; Shimoda M; Urakami K; Kowa H; Nakashima K
    Neurosci Lett; 2004 Sep; 368(3):319-22. PubMed ID: 15364419
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biological effects of four PSEN1 gene mutations causing Alzheimer disease with spastic paraparesis and cotton wool plaques.
    Dumanchin C; Tournier I; Martin C; Didic M; Belliard S; Carlander B; Rouhart F; Duyckaerts C; Pellissier JF; Latouche JB; Hannequin D; Frebourg T; Tosi M; Campion D
    Hum Mutat; 2006 Oct; 27(10):1063. PubMed ID: 16941492
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations.
    Houlden H; Baker M; McGowan E; Lewis P; Hutton M; Crook R; Wood NW; Kumar-Singh S; Geddes J; Swash M; Scaravilli F; Holton JL; Lashley T; Tomita T; Hashimoto T; Verkkoniemi A; Kalimo H; Somer M; Paetau A; Martin JJ; Van Broeckhoven C; Golde T; Hardy J; Haltia M; Revesz T
    Ann Neurol; 2000 Nov; 48(5):806-8. PubMed ID: 11079548
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis.
    Ataka S; Tomiyama T; Takuma H; Yamashita T; Shimada H; Tsutada T; Kawabata K; Mori H; Miki T
    Arch Neurol; 2004 Nov; 61(11):1773-6. PubMed ID: 15534188
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Alzheimer's disease with spastic paresis and cotton wool type plaques.
    Tabira T; Chui DH; Nakayama H; Kuroda S; Shibuya M
    J Neurosci Res; 2002 Nov; 70(3):367-72. PubMed ID: 12391599
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variable phenotype of Alzheimer's disease with spastic paraparesis.
    Smith MJ; Kwok JB; McLean CA; Kril JJ; Broe GA; Nicholson GA; Cappai R; Hallupp M; Cotton RG; Masters CL; Schofield PR; Brooks WS
    Ann Neurol; 2001 Jan; 49(1):125-9. PubMed ID: 11198283
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel mutation (G217D) in the Presenilin 1 gene ( PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum.
    Takao M; Ghetti B; Hayakawa I; Ikeda E; Fukuuchi Y; Miravalle L; Piccardo P; Murrell JR; Glazier BS; Koto A
    Acta Neuropathol; 2002 Aug; 104(2):155-70. PubMed ID: 12111359
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Alzheimer's disease with spastic paraparesis and 'cotton wool' plaques: two pedigrees with PS-1 exon 9 deletions.
    Brooks WS; Kwok JB; Kril JJ; Broe GA; Blumbergs PC; Tannenberg AE; Lamont PJ; Hedges P; Schofield PR
    Brain; 2003 Apr; 126(Pt 4):783-91. PubMed ID: 12615638
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variations in the neuropathology of familial Alzheimer's disease.
    Shepherd C; McCann H; Halliday GM
    Acta Neuropathol; 2009 Jul; 118(1):37-52. PubMed ID: 19306098
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Presenilin-1 mutations in Alzheimer's disease: an update on genotype-phenotype relationships.
    Larner AJ
    J Alzheimers Dis; 2013; 37(4):653-9. PubMed ID: 23948899
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of a presenilin 1 S170F mutation with a novel Alzheimer disease molecular phenotype.
    Piccini A; Zanusso G; Borghi R; Noviello C; Monaco S; Russo R; Damonte G; Armirotti A; Gelati M; Giordano R; Zambenedetti P; Russo C; Ghetti B; Tabaton M
    Arch Neurol; 2007 May; 64(5):738-45. PubMed ID: 17502474
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.
    Gallo M; Frangipane F; Cupidi C; De Bartolo M; Turone S; Ferrari C; Nacmias B; Grimaldi G; Laganà V; Colao R; Bernardi L; Anfossi M; Conidi ME; Vasso F; Curcio SAM; Mirabelli M; Smirne N; Torchia G; Muraca MG; Puccio G; Di Lorenzo R; Piccininni M; Tedde A; Maletta RG; Sorbi S; Bruni AC
    Neurobiol Aging; 2017 Aug; 56():213.e7-213.e12. PubMed ID: 28532646
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Alzheimer disease: autosomal dominant forms].
    Guyant-Maréchal L; Campion D; Hannequin D
    Rev Neurol (Paris); 2009 Mar; 165(3):223-31. PubMed ID: 19081588
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Presenilin-1 mutation Alzheimer's disease: a genetic epilepsy syndrome?
    Larner AJ
    Epilepsy Behav; 2011 May; 21(1):20-2. PubMed ID: 21501974
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and Molecular Findings in a Turkish Family Who Had a (c.869- 1G>A) Splicing Variant in PSEN1 Gene with A Rare Condition: The Variant Alzheimer's Disease with Spastic Paraparesis.
    Doğan M; Eröz R; Tecellioğlu M; Gezdirici A; Çevik B; Barış İ
    Curr Alzheimer Res; 2022; 19(3):223-235. PubMed ID: 35430993
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Young adult-onset, very slowly progressive cognitive decline with spastic paraparesis in Alzheimer's disease with cotton wool plaques due to a novel presenilin1 G417S mutation.
    Miki T; Yokota O; Haraguchi T; Ikeuchi T; Zhu B; Takenoshita S; Terada S; Yamada N
    Acta Neuropathol Commun; 2019 Feb; 7(1):19. PubMed ID: 30755281
    [No Abstract]   [Full Text] [Related]  

  • 20. Variant Alzheimer disease with spastic paraparesis: neuropathological phenotype.
    Verkkoniemi A; Kalimo H; Paetau A; Somer M; Iwatsubo T; Hardy J; Haltia M
    J Neuropathol Exp Neurol; 2001 May; 60(5):483-92. PubMed ID: 11379823
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.