Item does not contain fulltextBACKGROUND: Sedoheptulose, arabitol, ribitol, and erythritol have been identified as key diagnostic metabolites in TALDO deficiency. METHOD: Urine from 6 TALDO-deficient patients and TALDO-deficient knock-out mice were analyzed using (1)H-NMR spectroscopy and GC-mass spectrometry. RESULTS: Our data confirm the known metabolic characteristics in TALDO-deficient patients. The beta-furanose form was the major sedoheptulose anomer in TALDO-deficient patients. Erythronic acid was identified as a major abnormal metabolite in all patients and in knock-out TALDO mice implicating an as yet unknown biochemical pathway in this disease. A putative sequence of enzymatic reactions leading to the formation of erythronic acid ...
Methylmalonic acidurias represent a group of rare inborn errors of metabolism caused by deficient ac...
Defects in the gene encoding the persulfide dioxygenase ETHE1 are known to cause the severe inherite...
Alkaptonuria (AKU) is an inherited disorder of tyrosine metabolism caused by lack of active enzyme h...
BACKGROUND: Sedoheptulose, arabitol, ribitol, and erythritol have been identified as key diagnostic ...
AbstractBackgroundSedoheptulose, arabitol, ribitol, and erythritol have been identified as key diagn...
Abstract Transaldolase (TALDO) deficiency is a rare meta-bolic disease in the pentose phosphate path...
To access publisher's full text version of this article click on the hyperlink belowInborn errors of...
BackgroundTransaldolase deficiency (TALDO-D) is a rare autosomal recessive inborn error of the pento...
BACKGROUND: Transaldolase deficiency (TALDO-D) is a rare autosomal recessive inborn error of the pen...
BACKGROUND: Transaldolase deficiency (TALDO-D) is a rare autosomal recessive inborn error of the pen...
This article describes the first patient with a deficiency of transaldolase (TALDO1 [E.C.2.2.1.2]). ...
This article describes the first patient with a deficiency of transaldolase (TALDO1 [E.C.2.2.1.2]). ...
MSc (Biochemistry), North-West University, Potchefstroom CampusMitochondrial diseases (MDs) are the ...
polyol profiles in body fluids have been reported, but the origins of these polyols are unknown. We ...
Metabolic dysfunction burdens tissues with high energy demands, particularly the brain. Leigh syndro...
Methylmalonic acidurias represent a group of rare inborn errors of metabolism caused by deficient ac...
Defects in the gene encoding the persulfide dioxygenase ETHE1 are known to cause the severe inherite...
Alkaptonuria (AKU) is an inherited disorder of tyrosine metabolism caused by lack of active enzyme h...
BACKGROUND: Sedoheptulose, arabitol, ribitol, and erythritol have been identified as key diagnostic ...
AbstractBackgroundSedoheptulose, arabitol, ribitol, and erythritol have been identified as key diagn...
Abstract Transaldolase (TALDO) deficiency is a rare meta-bolic disease in the pentose phosphate path...
To access publisher's full text version of this article click on the hyperlink belowInborn errors of...
BackgroundTransaldolase deficiency (TALDO-D) is a rare autosomal recessive inborn error of the pento...
BACKGROUND: Transaldolase deficiency (TALDO-D) is a rare autosomal recessive inborn error of the pen...
BACKGROUND: Transaldolase deficiency (TALDO-D) is a rare autosomal recessive inborn error of the pen...
This article describes the first patient with a deficiency of transaldolase (TALDO1 [E.C.2.2.1.2]). ...
This article describes the first patient with a deficiency of transaldolase (TALDO1 [E.C.2.2.1.2]). ...
MSc (Biochemistry), North-West University, Potchefstroom CampusMitochondrial diseases (MDs) are the ...
polyol profiles in body fluids have been reported, but the origins of these polyols are unknown. We ...
Metabolic dysfunction burdens tissues with high energy demands, particularly the brain. Leigh syndro...
Methylmalonic acidurias represent a group of rare inborn errors of metabolism caused by deficient ac...
Defects in the gene encoding the persulfide dioxygenase ETHE1 are known to cause the severe inherite...
Alkaptonuria (AKU) is an inherited disorder of tyrosine metabolism caused by lack of active enzyme h...