Inflammatory status is one of the main drivers in the development of non-communicable
diseases (NCDs). Specific unhealthy dietary patterns and the growing consumption of ultra …

Hepatic glycogenosis (HG) in type 1 diabetes is a underrecognized complication. Mauriac
firstly described the syndrome characterized by hepatomegaly with altered liver enzymes …

A life-long dietary intervention can affect the substrates' availability for gut fermentation in
metabolic diseases such as the glycogen-storage diseases (GSD). Besides drug …

Glycogen storage diseases (GSDs) are a group of carbohydrate metabolism disorders, most
of which are inherited in autosomal recessive patterns. GSDs are of two types: those that …

Patients and Methods: A retrospective chart review of 32 GSD-I patients, followed at the
American University of Beirut Medical Center, between 2007 and 2018 was conducted …

Hepatic glycogen storage diseases (GSDs) are inborn errors of metabolism whose dietary
treatment involves uncooked cornstarch administration and restriction of simple …

Hypoxia and Inflammation are strictly interconnected with important consequences at clinical
and therapeutic level. While cell and tissue damage due to acute hypoxia mostly leads to …

Metabolic disorders, whether hereditary or acquired, affect the brain, and abnormalities of
the brain are related to cellular integrity; particularly in regard to neurons and astrocytes as …

Background Glycogen storage disease type I (GSDI) is caused by deficiency of the enzyme
glucose-6-phosphatase or glucose-6-phosphate transporter. Mainstay of treatment is …

Inborn errors of metabolism (IEMs) are rare hereditary or acquired disorders resulting from
an enzymatic deformity in biochemical and metabolic pathways influencing proteins, fats …