No association between catechol-O-methyltransferase (COMT) genotype and attention deficit hyperactivity disorder (ADHD) in Japanese children-Reference-Cited by-同舟云学术

No association between catechol-O-methyltransferase (COMT) genotype and attention deficit hyperactivity disorder (ADHD) in Japanese children

Published:2014-08 Issue:7 Volume:36 Page:620-625
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Yatsuga Chiho,Toyohisa Daiki,Fujisawa Takashi X.,Nishitani Shota,Shinohara Kazuyuki,Matsuura Naomi,Ikeda Shinobu,Muramatsu Masaaki,Hamada Akinobu,Tomoda Akemi

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

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1. Val158Met polymorphisms of COMT gene and serum concentrations of catecholaminergic neurotransmitters of ADHD in Chinese children and adolescents;Medicine;2021-12-10

2. Association of Val158Met polymorphism in COMT gene with attention-deficit hyperactive disorder;Medicine;2020-11-25

3. Genetic Influence on Efficacy of Pharmacotherapy for Pediatric Attention-Deficit/Hyperactivity Disorder: Overview and Current Status of Research;CNS Drugs;2020-03-04

4. PharmGKB summary;Pharmacogenetics and Genomics;2019-08

5. Methylphenidate for attention deficit hyperactivity disorder (ADHD) in children and adolescents - assessment of adverse events in non-randomised studies;Cochrane Database of Systematic Reviews;2018-05-10