These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

237 related articles for article (PubMed ID: 19797784)

  • 1. Novel PSEN1 mutation in a Bulgarian patient with very early-onset Alzheimer's disease, spastic paraparesis, and extrapyramidal signs.
    Dintchov Traykov L; Mehrabian S; Van den Broeck M; Radoslavova Raycheva M; Cruts M; Kirilova Jordanova A; Van Broeckhoven C
    Am J Alzheimers Dis Other Demen; 2009; 24(5):404-7. PubMed ID: 19797784
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update.
    Raux G; Guyant-Maréchal L; Martin C; Bou J; Penet C; Brice A; Hannequin D; Frebourg T; Campion D
    J Med Genet; 2005 Oct; 42(10):793-5. PubMed ID: 16033913
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A novel presenilin 1 mutation (V261L) associated with presenile Alzheimer's disease and spastic paraparesis.
    Jiménez Caballero PE; Lladó A; de Diego Boguna C; Martin Correa E; Serviá Candela M; Marsal Alonso C
    Eur J Neurol; 2008 Sep; 15(9):991-4. PubMed ID: 18637955
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland.
    Zekanowski C; Styczyńska M; Pepłońska B; Gabryelewicz T; Religa D; Ilkowski J; Kijanowska-Haładyna B; Kotapka-Minc S; Mikkelsen S; Pfeffer A; Barczak A; Łuczywek E; Wasiak B; Chodakowska-Zebrowska M; Gustaw K; Łaczkowski J; Sobów T; Kuźnicki J; Barcikowska M
    Exp Neurol; 2003 Dec; 184(2):991-6. PubMed ID: 14769392
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Early-onset familial Alzheimer's disease with spastic paraparesis associated with PSEN1 gene].
    Rudenskaya GE; Petukhova MS; Zabnenkova VV; Cherevatova TB; Ryzhkova OP
    Zh Nevrol Psikhiatr Im S S Korsakova; 2023; 123(11):120-127. PubMed ID: 37994898
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The genetics of very early onset Alzheimer disease.
    Filley CM; Rollins YD; Anderson CA; Arciniegas DB; Howard KL; Murrell JR; Boyer PJ; Kleinschmidt-DeMasters BK; Ghetti B
    Cogn Behav Neurol; 2007 Sep; 20(3):149-56. PubMed ID: 17846513
    [TBL] [Abstract][Full Text] [Related]  

  • 11. What is 'early onset dementia'?
    Miyoshi K
    Psychogeriatrics; 2009 Jun; 9(2):67-72. PubMed ID: 19604328
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel mutation in the PSEN2 gene (T430M) associated with variable expression in a family with early-onset Alzheimer disease.
    Ezquerra M; Lleó A; Castellví M; Queralt R; Santacruz P; Pastor P; Molinuevo JL; Blesa R; Oliva R
    Arch Neurol; 2003 Aug; 60(8):1149-51. PubMed ID: 12925374
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotype-phenotype analysis in early-onset Alzheimer's disease due to presenilin-1 mutations at codon 139.
    Hanisch F; Kölmel HW
    Eur J Med Res; 2004 Jul; 9(7):361-4. PubMed ID: 15337637
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DGGE method for the mutational analysis of the coding and proximal promoter regions of the Alzheimer's disease presenilin-1 gene: two novel mutations.
    Aldudo J; Bullido MJ; Valdivieso F
    Hum Mutat; 1999; 14(5):433-9. PubMed ID: 10533070
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel presenilin1 mutation (Q223R) associated with early onset Alzheimer's disease, dysarthria and spastic paraparesis and decreased Abeta levels in CSF.
    Uttner I; Kirchheiner J; Tumani H; Mottaghy FM; Lebedeva E; Ozer E; Ludolph AC; Huber R; von Arnim CA
    Eur J Neurol; 2010 Apr; 17(4):631-3. PubMed ID: 19912322
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two novel presenilin 1 gene mutations connected with frontotemporal dementia-like clinical phenotype: genetic and bioinformatic assessment.
    Zekanowski C; Golan MP; Krzyśko KA; Lipczyńska-Łojkowska W; Filipek S; Kowalska A; Rossa G; Pepłońska B; Styczyńska M; Maruszak A; Religa D; Wender M; Kulczycki J; Barcikowska M; Kuźnicki J
    Exp Neurol; 2006 Jul; 200(1):82-8. PubMed ID: 16546171
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Enhanced brain activity may precede the diagnosis of Alzheimer's disease by 30 years.
    Mondadori CR; Buchmann A; Mustovic H; Schmidt CF; Boesiger P; Nitsch RM; Hock C; Streffer J; Henke K
    Brain; 2006 Nov; 129(Pt 11):2908-22. PubMed ID: 17012294
    [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. Very Early-Onset Alzheimer's Disease in the Third Decade of Life with de novo PSEN1 Mutations.
    Chen KL; Li PX; Sun YM; Chen SF; Zuo CT; Wang J; Dong Q; Cui M; Yu JT
    J Alzheimers Dis; 2022; 85(1):65-71. PubMed ID: 34776449
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.