Volume 12 (2024)
Volume 11 (2023)
Volume 10 (2022)
Volume 9 (2021)
Volume 8 (2020)
Volume 7 (2019)
Volume 6 (2018)
Volume 5 (2017)
Volume 4 (2016)
Volume 3 (2015)
Volume 2 (2014)
Volume 1 (2013)
Author = Leila Mehdizadeh Fanid
Number of Articles: 8
The rs6323 and uVNTR Polymorphisms in the MAOA Gene are Associated with Attention Deficit Hyperactivity Disorder in Iranian Azeri Children
Volume 10, Issue 9 , September 2022, , Pages 16712-16718
Abstract
Background: ADHD is the most prevalent psychiatric health issue in youth, which may also affect adults. Environmental and genetic factors both contribute significantly to the development ... Read More
Polymorphism of dopamine transporter gene 3'-UTR VNTR in Iranian Azeri Turkish patients with ADHD
Volume 10, Issue 2 , February 2022, , Pages 15466-15473
Abstract
Background: Attention Deficit Hyperactivity Disorder (ADHD) is the most common neurobehavioral disorder among children, which several studies have indicated the role of genetic factors ... Read More
The Survey of DBH Gene Polymorphism Rs5320 in Children with Attention Deficit Hyperactivity Disorder (ADHD)
Volume 6, Issue 9 , September 2018, , Pages 8177-8184
Abstract
Background Attention deficit hyperactivity disorder (ADHD) is a common behavioral disorder that affects 8-12% of school-age children. Several environmental and genetic factors play ... Read More
Evaluating Sleep Disorders amongst Children with Attention Deficit/ Hyperactivity Disorder (ADHD)
Volume 5, Issue 10 , October 2017, , Pages 5907-5917
Abstract
Background: The attention deficit/ hyperactivity disorder (ADHD) is one of the most compromising mental disorders of childhood and adolescence. Subsequently, different studies in recent ... Read More
Study of Polymorphism of the DRD2 Gene (-141C Ins/Del, rs1799732) with Attention Deficit Hyperactivity Disorder a Population Sample of Children in Iranian-Azeri
Volume 5, Issue 3 , March 2017, , Pages 4569-4574
Abstract
BackgroundAttention deficit hyperactivity disorder (ADHD), is a multifactorial disorder and converging evidence has implicated abnormalities of dopamine neurotransmission. The aim of ... Read More
An Association Analysis of Reelin Gene (RELN) Exon 22 (G/C), Rs.362691, Polymorphism with Autism Spectrum Disorder among Iranian-Azeri Population
Volume 4, Issue 7 , July 2016, , Pages 2027-2033
Abstract
Background Autism spectrum disorder (ASD) is a intricate childhood neuropsychiatric disorder that is described by deficits in communication of verbal and non-verbal, reciprocal social ... Read More
The Association of DRD2 Gene TaqI Polymorphism with Attention Deficit Hyperactivity Disorder a Population Sample of Iranian Azeri-children
Volume 4, Issue 5 , May 2016, , Pages 1803-1807
Abstract
Background Attention deficit hyperactivity disorder (ADHD) is a multi-factorial disorder that has defined by hyperactivity, impulsivity and attention deficits. Various neurotransmitters ... Read More
Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients
Volume 3, Issue 6.1 , November 2015, , Pages 1065-1071