Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Dementia and NOS3[original query] |
---|
Nitric oxide synthase gene polymorphisms in Alzheimer's disease and dementia with Lewy bodies. Neuroscience letters 2001 Apr 303 (1): 33-6. Singleton AB, Gibson AM, McKeith IG, Ballard CG, Edwardson JA, Morris CM |
Pharmacogenomics for the treatment of dementia. Annals of medicine 2002 34 (5): 357-79. Cacabelos Ram |
The nitric oxide synthase-3 codon 298 polymorphism is not associated with late-onset sporadic Alzheimer's dementia and Lewy body disease in a sample from Hungary. Psychiatric genetics 2003 Dec 13 (4): 201-4. Kálmán János, Juhász Anna, Rimanóczy Agnes, Palotás András, Palotás Miklós, Boda Krisztina, Márki-Zay János, Csibri Eva, Janka Zolt |
Poorer cognitive performance in humans with mild cognitive impairment carrying the T variant of the Glu/Asp NOS3 polymorphism. Neuroscience letters 2004 Mar 358 (1): 5-8. Solé-Padullés C, Bartrés-Faz D, Junqué C, Via M, Matarín M, González-Pérez E, Moral P, Moya A, Clemente IC |
NOS3 gene rs1799983 polymorphism and incident dementia in elderly stroke survivors. Neurobiology of aging 2011 Mar 32 (3): 554.e1-6. Morris Christopher M, Ballard Clive G, Allan Louise, Rowan Elise, Stephens Sally, Firbank Michael, Ford Gary A, Kenny Rose Anne, O'Brien John T, Kalaria Raj |
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
Stroke 2020 07 51 (7): 2111-2121. Armstrong Nicola J, Mather Karen A, Sargurupremraj Muralidharan, Knol Maria J, Malik Rainer, Satizabal Claudia L, Yanek Lisa R, Wen Wei, Gudnason Vilmundur G, Dueker Nicole D, Elliott Lloyd T, Hofer Edith, Bis Joshua, Jahanshad Neda, Li Shuo, Logue Mark A, Luciano Michelle, Scholz Markus, Smith Albert V, Trompet Stella, Vojinovic Dina, Xia Rui, Alfaro-Almagro Fidel, Ames David, Amin Najaf, Amouyel Philippe, Beiser Alexa S, Brodaty Henry, Deary Ian J, Fennema-Notestine Christine, Gampawar Piyush G, Gottesman Rebecca, Griffanti Ludovica, Jack Clifford R, Jenkinson Mark, Jiang Jiyang, Kral Brian G, Kwok John B, Lampe Leonie, C M Liewald David, Maillard Pauline, Marchini Jonathan, Bastin Mark E, Mazoyer Bernard, Pirpamer Lukas, Rafael Romero José, Roshchupkin Gennady V, Schofield Peter R, Schroeter Matthias L, Stott David J, Thalamuthu Anbupalam, Trollor Julian, Tzourio Christophe, van der Grond Jeroen, Vernooij Meike W, Witte Veronica A, Wright Margaret J, Yang Qiong, Morris Zoe, Siggurdsson Siggi, Psaty Bruce, Villringer Arno, Schmidt Helena, Haberg Asta K, van Duijn Cornelia M, Jukema J Wouter, Dichgans Martin, Sacco Ralph L, Wright Clinton B, Kremen William S, Becker Lewis C, Thompson Paul M, Mosley Thomas H, Wardlaw Joanna M, Ikram M Arfan, Adams Hieab H H, Seshadri Sudha, Sachdev Perminder S, Smith Stephen M, Launer Lenore, Longstreth William, DeCarli Charles, Schmidt Reinhold, Fornage Myriam, Debette Stephanie, Nyquist Paul |
Analysis of Genotype-Phenotype Correlations in Patients With Degenerative Dementia Through the Whole Exome Sequencing. Frontiers in aging neuroscience 2021 11 13 745407. Sun Lin, Zhang Jianye, Su Ning, Zhang Shaowei, Yan Feng, Lin Xiang, Yu Jie, Li Wei, Li Xia, Xiao Shi |
Analysis of endothelial gene polymorphisms in Spanish patients with vascular dementia and Alzheimer´s disease. Scientific reports 2023 8 13 (1): 13441. Raquel Manso-Calderón, Purificación Cacabelos-Pérez, M Dolores Sevillano-García, M Elisa Herrero-Prieto, Rogelio González-Sarmien |
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 25, 2024
- Content source: