Associated Papers
The genetics of incontinence: A scoping review.
Breinbjerg A et al.
Clinical Genetics, 2023
Association of G84A and C276T polymorphism in neuronal nitric oxide synthase (nNOS) gene with herpes simplex encephalitis in eastern Indian population.
Rathore SK et al.
Nitric Oxide : Biology and Chemistry, 2021
Endothelial nitric oxide synthase (-786T>C) polymorphism and migraine susceptibility: A meta-analysis.
Dong H et al.
Medicine, 2018
Updated meta-analysis of the role of APOE ε2/ε3/ε4 alleles in frontotemporal lobar degeneration.
Su WH et al.
Oncotarget, 2017
Single Nucleotide Polymorphisms in Pediatric Idiopathic Nephrotic Syndrome.
Suvanto M et al.
International Journal of Nephrology, 2016
Neuronal Nitric Oxide Synthase (nNOS, NOS1) rs693534 and rs7977109 Variants and Risk for Migraine.
García-Martín E et al.
Headache, 2015
Clinical significance of pharmacogenomic studies in tardive dyskinesia associated with patients with psychiatric disorders.
Chang FC et al.
Pharmacogenomics and Personalized Medicine, 2014
RNAsnp: efficient detection of local RNA secondary structure changes induced by SNPs.
Sabarinathan R et al.
Human Mutation, 2013
Common polymorphisms in nitric oxide synthase (NOS) genes influence quality of aging and longevity in humans.
Montesanto A et al.
Biogerontology, 2013
Lack of association between the C276T polymorphism of the neuronal nitric oxide synthase gene and migraine.
Alaşehirli B et al.
The International Journal of Neuroscience, 2013
Frontotemporal lobar degeneration: current knowledge and future challenges.
Cerami C et al.
Journal of Neurology, 2012
Behavioral genetics of neurodegenerative disorders.
Galimberti D et al.
Current Topics in Behavioral Neurosciences, 2012
Genetics of frontotemporal lobar degeneration.
Galimberti D et al.
Frontiers in Neurology, 2012
Genetic polymorphisms in DNA repair and oxidative stress pathways associated with malignant melanoma susceptibility.
Ibarrola-Villava M et al.
European Journal of Cancer (oxford, England : 1990), 2011
Genomic variants in the coding region of neuronal nitric oxide synthase (NOS1) in infantile hypertrophic pyloric stenosis.
Serra A et al.
Journal of Pediatric Surgery, 2011
Inflammation and oxidative damage in Alzheimer's disease: friend or foe?
Galimberti D et al.
Frontiers in Bioscience (scholar Edition), 2011
Association study of xenobiotic detoxication and repair genes with malignant brain tumors in children.
Salnikova LE et al.
Acta Naturae, 2010
Genetics and biology of Alzheimer's disease and frontotemporal lobar degeneration.
Galimberti D et al.
International Journal of Clinical and Experimental Medicine, 2010
Genetic association analysis of functional polymorphisms in neuronal nitric oxide synthase 1 gene (NOS1) and mood disorders and fluvoxamine response in major depressive disorder in the Japanese population.
Okumura T et al.
Neuropsychobiology, 2010
Genetic variation in neuronal nitric oxide synthase (nNOS) gene and susceptibility to cerebral malaria in Indian adults.
Dhangadamajhi G et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases, 2009
Nitric oxide synthase gene polymorphisms in children with minimal change nephrotic syndrome.
Alasehirli B et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2009
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration.
Venturelli E et al.
European Journal of Neurology, 2009
Association of a NOS1 promoter repeat with Alzheimer's disease.
Galimberti D et al.
Neurobiology of Aging, 2008
Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degeneration.
Borroni B et al.
Rejuvenation Research, 2008
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.
Venturelli E et al.
European Journal of Neurology, 2008
Nitric oxide synthase gene polymorphisms in children with primary nocturnal enuresis: a preliminary study.
Balat A et al.
Renal Failure, 2007
Association of neuronal nitric oxide synthase C276T polymorphism with Alzheimer's disease.
Galimberti D et al.
Journal of Neurology, 2005
Association analysis of a neural nitric oxide synthase gene polymorphism and antipsychotics-induced tardive dyskinesia in Chinese schizophrenic patients.
Wang YC et al.
Journal of Neural Transmission (vienna, Austria : 1996), 2004
Association analysis for neuronal nitric oxide synthase gene polymorphism with major depression and fluoxetine response.
Yu YW et al.
Neuropsychobiology, 2003
Recent advances in the molecular genetics of frontotemporal lobar degeneration.
Rainero I et al.
Functional Neurology, 0