Neurologically normal development of a patient with severe methionine adenosyltransferase I/III deficiency after continuing dietary methionine restriction - ScienceDirect
Determination of Autosomal Dominant or Recessive Methionine Adenosyltransferase I/III Deficiencies Based on Clinical and Molecular Studies | Molecular Medicine | Full Text
Frontiers | Long-term prognosis of 35 patients with methionine adenosyltransferase deficiency based on newborn screening in China
CBS, MET Act Sheet
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes | Orphanet Journal of Rare Diseases | Full Text
Characterization of MAT I/III deficient patients' relatives | Download Scientific Diagram
Methionine Adenosyltransferase - an overview | ScienceDirect Topics
Neurologically normal development of a patient with severe methionine adenosyltransferase I/III deficiency after continuing dietary methionine restriction. | Semantic Scholar
Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders | Journal of Inherited Metabolic Disease
Organic Acid Disorders
Metabolism of the Sulfur-Containing Amino Acids. 1, methionine... | Download Scientific Diagram
Analysis of vitamin D status at two academic medical centers and a national reference laboratory: result patterns vary by age, gender, season, and patient location – topic of research paper in Clinical
Determination of Autosomal Dominant or Recessive Methionine Adenosyltransferase i/iii Deficiencies Based on Clinical and Molecul
Methionine adenosyltransferase I/III deficiency: Neurological manifestations and relevance of S-adenosylmethionine - ScienceDirect
Methionine Adenosyltransferase I/III Deficiency in Portugal: High Frequency of a Dominantly Inherited Form in a Small Area of Douro High Lands | SpringerLink
Bone Marrow Adipose Tissue Deficiency Increases Disuse-Induced Bone Loss in Male Mice | Scientific Reports
Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene. - Abstract - Europe PMC
BKD (beta-ketothiolase deficiency) – newbornscreening.info
Methionine adenosyltransferases in cancers: Mechanisms of dysregulation and implications for therapy | Semantic Scholar
Redbubble for Sale | Redbubble
Yoga Can Improve Iron Deficiency and Anemia | Yoga Janda
Fructose-1,6-Diphosphatase Deficiency Misdiagnosed as Reye Syndrome - Enrico Zammarchi, Maria A. Donati, Federica Ciani, Pietro Rubetti, Elisabetta Pasquini, 1995
Hypermethioninemia: MedlinePlus Genetics
