Results 81 to 90 of about 26,853 (215)
ABSTRACT Fragile X Syndrome (FXS), an X‐linked genetic condition, is associated with a wide range of phenotypic manifestations, namely intellectual disability (ID), autism spectrum disorder (ASD), attention deficit hyperactivity disorder (ADHD), and atypical behaviors.
Mélodie Proteau‐Lemieux +14 more
wiley +1 more source
Effects of sulpiride and methylphenidate on brain and cognition: a PET pharmaco-fMRI study
Jessica I. Määttä +6 more
openalex +1 more source
Methylphenidate Treatment in ADHD/borderline Personality Disorder Adolescent Girls and Smoking Behavior [PDF]
Pavel Golubchik +4 more
openalex +1 more source
Methylphenidate hydrochloride and asymptomatic ocular changes
Objective: To examine cataract formation and assess intraocular pressure (IOP) measurement with Goldmann applanation tonometry in children taking methylphenidate hydrochloride. Methods: Forty children with attention deficit hyperactivity disorder aged
Nagihan Saday Duman +8 more
doaj
Psychoactive prescription drug use and misuse in patients on opioid agonist treatment
Aims To identify the patterns and trends in prescription drug use and misuse in patients on opioid agonist treatment. Methods We used data from the OPPIDUM programme, which collects data from patients attending substance abuse treatment facilities. Data collected include use of psychoactive prescription drugs in the past week.
Thomas Soeiro +5 more
wiley +1 more source
Effect of Oral Methylphenidate on the Experimental Epileptiform Activity in Male Rats [PDF]
Yousef Panahi +2 more
openalex +1 more source
ABSTRACT Cancer was the second leading cause of death worldwide in 2018 according to WHO. The disease burden continues to grow and has tremendous impacts on families and healthcare systems. Cancer‐related fatigue is one of the most distressing symptoms experienced by cancer patients and has adverse impacts on the patients' quality of life and ...
Benjamin K. K. Lau +3 more
wiley +1 more source
ABSTRACT Smith‐Magenis Syndrome (SMS) is an uncommon genetic disorder caused by microdeletions of chromosome 17p11.2 including the RAI1 gene, or loss‐of‐function mutations that directly affect RAI1. Due to the involvement of RAI1 in neurodevelopment, SMS leads to typical pathologic features in the behavioral and physical phenotype that must be ...
Edgar Andrés Chavarría‐Martínez +4 more
wiley +1 more source
Chronic methylphenidate treatment during adolescence has long-term effects on monoaminergic function [PDF]
Mathieu Di Miceli +2 more
openalex +1 more source

