Results 141 to 150 of about 4,728 (183)
Some of the next articles are maybe not open access.
Melaminium glutarate monohydrate
Acta Crystallographica Section C Crystal Structure Communications, 2002The crystal structure of the title new melaminium salt, 2,4,6-triamino-1,3,5-triazin-1-ium glutarate monohydrate, C(3)H(7)N(6)(+) x C(5)H(7)O(4)(-) x H(2)O, is built up from singly protonated melaminium residues, mono-dissociated glutarate ions and water molecules.
Jan, Janczak, Genivaldo Julio, Perpétuo
openaire +2 more sources
Significance of bound glutarate in the diagnosis of glutaric aciduria type I
Journal of Inherited Metabolic Disease, 1992Glutaric aciduria type I (GA-I) (McKusick 231670) is an autosomal recessive disorder caused by glutaryl-CoA dehydro genase (GD) deficiency. The diagnosis of GA-I is determined by organic acid analysis of urine and is confirmed by measuring the enzyme activity in cultured skin fibroblasts or leukocytes.
Ribes A +5 more
openaire +3 more sources
Journal of Solution Chemistry, 2007
Conductivity measurements of glutaric acid and disodium glutarate in dilute aqueous solutions were performed in the 288.15 to 323.15 K temperature range. The limiting equivalent conductances of glutarate anions, λo(HGlut−,T) and λo(1/2Glut2−,T), and the dissociation constants of glutaric acid, K1(T) and K2(T), were derived by the use of the Onsager and
Alexander Apelblat +2 more
openaire +1 more source
Conductivity measurements of glutaric acid and disodium glutarate in dilute aqueous solutions were performed in the 288.15 to 323.15 K temperature range. The limiting equivalent conductances of glutarate anions, λo(HGlut−,T) and λo(1/2Glut2−,T), and the dissociation constants of glutaric acid, K1(T) and K2(T), were derived by the use of the Onsager and
Alexander Apelblat +2 more
openaire +1 more source
The Journal of Pediatrics, 1980
Two infants have been studied with glutaric aciduria Type II. The clinical presentation was of an overwhelming illness very early in life; both infants died in the neonatal period. One had dysmorphic features. An acrid odor may be a clue to the diagnosis. Neonatal acidosis, hypoglycemia, and hyperammonemia are characteristic.
L, Sweetman +4 more
openaire +2 more sources
Two infants have been studied with glutaric aciduria Type II. The clinical presentation was of an overwhelming illness very early in life; both infants died in the neonatal period. One had dysmorphic features. An acrid odor may be a clue to the diagnosis. Neonatal acidosis, hypoglycemia, and hyperammonemia are characteristic.
L, Sweetman +4 more
openaire +2 more sources
Neurology, 1980
A boy with glutaric acidemia had psychomotor retardation first noted at age 6 months, recurrent metabolic acidosis, and a progressive quadriparesis with choreoathetosis. He died at age 3 1/2 years. Cultured skin fibroblasts lacked glutaryl-CoA dehydrogenase activity. There was a biochemical, but not a clinical, response to dietary restriction of lysine
R L, Leibel +7 more
openaire +2 more sources
A boy with glutaric acidemia had psychomotor retardation first noted at age 6 months, recurrent metabolic acidosis, and a progressive quadriparesis with choreoathetosis. He died at age 3 1/2 years. Cultured skin fibroblasts lacked glutaryl-CoA dehydrogenase activity. There was a biochemical, but not a clinical, response to dietary restriction of lysine
R L, Leibel +7 more
openaire +2 more sources