Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Zainunisha Arieff"'
Publikováno v:
Journal of Medical Primatology. 45:189-194
Background Non-ketotic hyperglycinaemia (NKH) is an autosomal recessive inborn error of glycine metabolism characterized by accumulation of glycine in body fluids and various neurological symptoms. Methods This study describes the first screening of
Autor:
Lize van der Merwe, Hajirah Gameeldien, Muneera Davids, Jyoti R. Sharma, Zainunisha Arieff, Mandeep Kaur
Publikováno v:
Genetic Testing and Molecular Biomarkers. 17:93-98
Background: Autism (MIM209850) is a neurodevelopmental disorder characterized by a triad of impairments, namely impairment in social interaction, impaired communication skills, and restrictive and repetitive behavior. A number of family and twin stud
Publikováno v:
Journal of Neural Transmission. 115:755-760
The serotonin transporter promoter length polymorphism (5-hydroxytryptamine transporter length polymorphism, 5-HTTLPR) in serotonin transporter gene has been implicated in numerous psychiatric disorders. Having a high affinity for the neurotransmitte
Publikováno v:
Lab animal. 43(2)
Niacin is the most effective drug available for raising levels of high-density lipoprotein (HDL) cholesterol. To evaluate its effects on plasma lipid concentrations, the authors administered a low dose of niacin to healthy, adult, female African gree
Publikováno v:
Human biology. 82(3)
The serotonin transporter promoter length polymorphism (5-hydroxytryptamine transporter length polymorphism; 5-HTTLPR) has long been implicated in autism and other psychiatric disorders. The use of selective serotonin reuptake inhibitors (SSRIs) has
Publikováno v:
Autism Insights. :1