A patient with glutaric aciduria type I had an acute encephalopathic crisis despite early treatment. This report indicates that current therapeutic strategies may be insufficient for some high-risk patients and stresses the demand for new approaches in glutaric aciduria type I
Glutaric aciduria type 1 is a rare inherited neurometabolic disorder of lysine metabolism caused by ...
Glutaric aciduria type I (GA-I; synonym, glutaric acidemia type I) is a rare inherited metabolic dis...
Objective Glutaricaciduria type 1 (GA1), is a rare, treatable neuro metabolic disease, due to gluta...
Objectives: The impact of coronavirus disease-19 (COVID-19) on metabolic outcome in patients with in...
Glutaric aciduria type I (synonym, glutaric acidemia type I) is a rare organic aciduria. Untreated p...
Glutaric Aciduria type I (GA-I) is a rare organic acidemia, caused by mutations in the GCDH gene, an...
Glutaryl-CoA dehydrogenase (GCDH) deficiency is an autosomal recessive disease with an estimated ove...
Glutaric acidemia type I (GA-1) is a neurological disease of metabolic ethiology. Although considere...
Objective: Glutaric aciduria type 1 (GA1), is a rare, treatable neuro- metabolic disease, due to Glu...
Glutaric aciduria type 1 (GA1), resulting from the genetic deficiency of glutaryl-CoA dehydrogenase ...
Glutaric aciduria type 1 (GA1) is an organic acidaemia. The objective of this study was to describe ...
ABSTRACT: Glutaryl-CoA dehydrogenase (GCDH) deficiency is a rare neurometabolic disorder that is con...
Glutaric aciduria type I (GA-I) is an autosomal recessive genetic disorder caused by a deficiency in...
Glutaric aciduria type I (GA-I; synonym, glutaric acidemia type I) is a rare inherited metabolic dis...
Glutaric aciduria type I (GA-I) is an inborn error of lysine and tryptophan metabolism. Clinical man...
Glutaric aciduria type 1 is a rare inherited neurometabolic disorder of lysine metabolism caused by ...
Glutaric aciduria type I (GA-I; synonym, glutaric acidemia type I) is a rare inherited metabolic dis...
Objective Glutaricaciduria type 1 (GA1), is a rare, treatable neuro metabolic disease, due to gluta...
Objectives: The impact of coronavirus disease-19 (COVID-19) on metabolic outcome in patients with in...
Glutaric aciduria type I (synonym, glutaric acidemia type I) is a rare organic aciduria. Untreated p...
Glutaric Aciduria type I (GA-I) is a rare organic acidemia, caused by mutations in the GCDH gene, an...
Glutaryl-CoA dehydrogenase (GCDH) deficiency is an autosomal recessive disease with an estimated ove...
Glutaric acidemia type I (GA-1) is a neurological disease of metabolic ethiology. Although considere...
Objective: Glutaric aciduria type 1 (GA1), is a rare, treatable neuro- metabolic disease, due to Glu...
Glutaric aciduria type 1 (GA1), resulting from the genetic deficiency of glutaryl-CoA dehydrogenase ...
Glutaric aciduria type 1 (GA1) is an organic acidaemia. The objective of this study was to describe ...
ABSTRACT: Glutaryl-CoA dehydrogenase (GCDH) deficiency is a rare neurometabolic disorder that is con...
Glutaric aciduria type I (GA-I) is an autosomal recessive genetic disorder caused by a deficiency in...
Glutaric aciduria type I (GA-I; synonym, glutaric acidemia type I) is a rare inherited metabolic dis...
Glutaric aciduria type I (GA-I) is an inborn error of lysine and tryptophan metabolism. Clinical man...
Glutaric aciduria type 1 is a rare inherited neurometabolic disorder of lysine metabolism caused by ...
Glutaric aciduria type I (GA-I; synonym, glutaric acidemia type I) is a rare inherited metabolic dis...
Objective Glutaricaciduria type 1 (GA1), is a rare, treatable neuro metabolic disease, due to gluta...