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Hepatic methionine adenosyltransferase deficiency

Known as: METHIONINE ADENOSYLTRANSFERASE DEFICIENCY, Methioninemia, MAT I/III DEFICIENCY 
A metabolic disorder usually inherited in an autosomal recessive pattern and caused by mutations in the MAT1A gene. Affected individuals usually do… 
National Institutes of Health

Related topics

Related topics

13 relations
Amino acidemia disorder suspected:Prid:Pt:Bld.dot:NomAutosomal dominant inheritanceAutosomal recessive inheritanceConditions tested for in this newborn screening study:ID:Pt:Bld.dot:Nom

Broader (1)

Hypermethioninemia

Papers overview

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2011
2011
Supporting Native Indian Preschoolers and Their Families Family–School–Community Partnerships
M. Susan McWilliams, PhD, is an assistant professor at the University of Nebraska at Omaha. She serves as the facilitator of the… 
2011
2011
Broadband Electromagnetic Characterization of Materials for Accelerator Components
Electromagnetic (EM) characterization of materials up to high frequencies is a major requirement for the correct modeling of many… 
2010
2010
Achieving of Tabu Search Algorithm for Scheduling Technique in Grid Computing Using GridSim Simulation Tool: Multiple Jobs on Limited Resource
Grid computing is a form of distributed computing involves coordinating and sharing computing, application, data storage or… 
2001
2001
Biochemical Basis for the Dominant Inheritance of Hypermethioninemia Associated with the R264H Mutation of theMAT1A Gene
Methionine adenosyltransferase (MAT) catalyzes the synthesis of S-adenosylmethionine (AdoMet), the main alkylating agent in… 
1986
1986
Medication effects on one-carbon metabolism in schizophrenia, mania, and major depression.
Erythrocyte methionine adenosyltransferase (MAT) activity (Vmax) and phosphatidylcholine (PC) levels previously have been found… 
1984
1984
Hypermethioninemia Associated with Hepatic Methionine Adenosyltransferase Deficiency: Report of Two Cases
In two patients with persistent hypermethioninemia who were detected in a neonatal mass‐screening program, hepatic methionine… 
1984
1984
Methodik der radikalen transabdominalen Tumornephrektomie mat fakultativer oder systematischer lymphdissektion und deren Ergebnisse an 381 Patienten
Chez des malades avec hypernephrome sans metastase la survie a 3 et 5 ans a ete apres lymphadenectomie facultative de 64±8% et 50… 
1982
1982
A new type of hypermethioninemia in neonates.
Eleven hypermethioninemic patients were found by mass screening tests of neonates. Three of these had persistent… 
1978
1978
Dietary treatment of tyrosinemia type I: importance of methionine restriction.
A patient with tyrosinemia type I was treated with formula 3200 AB. This dietary approach lowered the elevated plasma… 
1969
1969
Hypermethioninemia with other hyperaminoacidemias. Studies in infants on high-protein diets.
HYPERMETHIONINEMIA in infancy occurs regularly with homocystinuria due to cystathionine synthase deficiency. 1,2 It has also been…