Lista de obras - Zsanett Tarnok - Dominio Público Uruguay

Association analysis of norepinephrine transporter polymorphisms and methylphenidate response in ADHD patients.

artículo científico publicado en 2018

Association between the 120-bp duplication of the dopamine D4 receptor gene and attention deficit hyperactivity disorder: Genetic and molecular analyses

article

Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort

artículo científico publicado en 2015

Association of the tumor necrosis factor -308 A/G promoter polymorphism with Tourette syndrome

artículo científico publicado en 2014

Catechol-O-methyltransferase Val158Met polymorphism is associated with methylphenidate response in ADHD children.

artículo científico publicado en 2008

Dopaminergic candidate genes in Tourette syndrome: Association between tic severity and 3′ UTR polymorphism of the dopamine transporter gene

article

Executive dysfunction in frontal lesions and frontal epilepsy

artículo científico publicado en 2006

Genetic association signal near NTN4 in Tourette syndrome

artículo científico publicado en 2014

Geographically separate increases in the frequency of the derived ADH1B*47His allele in eastern and western Asia

artículo científico publicado en 2007

Is procedural memory enhanced in Tourette syndrome? Evidence from a sequence learning task.

artículo científico publicado en 2017

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

artículo científico publicado en 2017

Reduced fronto-cortical brain connectivity during NREM sleep in Asperger syndrome: an EEG spectral and phase coherence study.

artículo científico publicado en 2010

Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families

artículo científico publicado en 2013

Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology

artículo científico publicado en 2016

The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.