Biochemical and developmental results of treatment of a guanidinoacetate methyltransferase (GAMT) deficient patient with a mild clinical presentation and remarkable developmental improvement after treatment are presented. Treatment with creatine (Cr) supplementation resulted in partial normalization of cerebral (measured with magnetic resonance proton spectroscopy) and plasma levels of Cr and guanidinoacetate (GAA). Addition of high dose ornithine to the treatment led to further normalization of plasma GAA, while cerebral Cr and GAA did not improve further. (c) 2007 Elsevier Inc. All rights reserved
Guanidinoacetate N-methyltransferase (GAMT) deficiency is a rare autosomal recessive disorder charac...
GAMT deficiency is a rare autosomal recessive disease within the group of cerebral creatine deficien...
Guanidinoactetate methyltransferase (GAMT) deficiency is an autosomal recessive disorder of creatine...
Biochemical and developmental results of treatment of a guanidinoacetate methyltransferase (GAMT) de...
Biochemical and developmental results of treatment of a guanidinoacetate methyltransferase (GAMT) de...
Biochemical and developmental results of treatment of a guanidinoacetate methyltransferase (GAMT) de...
Biochemical and developmental results of treatment of a guanidinoacetate methyltransferase (GAMT) de...
We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) def...
We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) def...
We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) def...
Guanidinoacetate methyltransferase (GAMT) deficiency is an autosomal recessive disorder caused by pa...
We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) def...
Creatine deficiency disorders are inborn errors of creatine metabolism, an energy homeostasis molecu...
Purpose Guanidinoacetate methyltransferase (GAMT) deficiency is an autosomal recessive disorder caus...
Purpose Guanidinoacetate methyltransferase (GAMT) deficiency is an autosomal recessive disorder caus...
Guanidinoacetate N-methyltransferase (GAMT) deficiency is a rare autosomal recessive disorder charac...
GAMT deficiency is a rare autosomal recessive disease within the group of cerebral creatine deficien...
Guanidinoactetate methyltransferase (GAMT) deficiency is an autosomal recessive disorder of creatine...
Biochemical and developmental results of treatment of a guanidinoacetate methyltransferase (GAMT) de...
Biochemical and developmental results of treatment of a guanidinoacetate methyltransferase (GAMT) de...
Biochemical and developmental results of treatment of a guanidinoacetate methyltransferase (GAMT) de...
Biochemical and developmental results of treatment of a guanidinoacetate methyltransferase (GAMT) de...
We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) def...
We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) def...
We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) def...
Guanidinoacetate methyltransferase (GAMT) deficiency is an autosomal recessive disorder caused by pa...
We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) def...
Creatine deficiency disorders are inborn errors of creatine metabolism, an energy homeostasis molecu...
Purpose Guanidinoacetate methyltransferase (GAMT) deficiency is an autosomal recessive disorder caus...
Purpose Guanidinoacetate methyltransferase (GAMT) deficiency is an autosomal recessive disorder caus...
Guanidinoacetate N-methyltransferase (GAMT) deficiency is a rare autosomal recessive disorder charac...
GAMT deficiency is a rare autosomal recessive disease within the group of cerebral creatine deficien...
Guanidinoactetate methyltransferase (GAMT) deficiency is an autosomal recessive disorder of creatine...