Frontiers | Long-term prognosis of 35 patients with methionine adenosyltransferase deficiency based on newborn screening in China
Organic Acid Disorders
Methionine adenosyltransferases in cancers: Mechanisms of dysregulation and implications for therapy | Semantic Scholar
MAT Deficiency: Wider effects of a rare disease
Yoga Can Improve Iron Deficiency and Anemia | Yoga Janda
Metabolism of the Sulfur-Containing Amino Acids. 1, methionine... | Download Scientific Diagram
BKD (beta-ketothiolase deficiency) – newbornscreening.info
Methionine adenosyltransferase I/III deficiency: Neurological manifestations and relevance of S-adenosylmethionine - ScienceDirect
Fructose-1,6-Diphosphatase Deficiency Misdiagnosed as Reye Syndrome - Enrico Zammarchi, Maria A. Donati, Federica Ciani, Pietro Rubetti, Elisabetta Pasquini, 1995
Neurologically normal development of a patient with severe methionine adenosyltransferase I/III deficiency after continuing dietary methionine restriction - ScienceDirect
Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations
Methionine, AdoMet, and AdoHcy metabolism. AdoMet, S-... | Download Scientific Diagram
CBS, MET Act Sheet
Methionine Adenosyltransferase - an overview | ScienceDirect Topics
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
Diagnostic Value of the MAT1A Gene Mutations in Methionine Adenosyltransferase I/III Deficiency: Possible Relevance to Various Neurological Manifestations
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes | Orphanet Journal of Rare Diseases | Full Text
Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene. - Abstract - Europe PMC
Determination of Autosomal Dominant or Recessive Methionine Adenosyltransferase i/iii Deficiencies Based on Clinical and Molecul
Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders | Journal of Inherited Metabolic Disease
Methionine Adenosyltransferase I/III Deficiency in Portugal: High Frequency of a Dominantly Inherited Form in a Small Area of Douro High Lands | SpringerLink
Never Ignore These Warning Signs Of Vitamin B12 Deficiency | B12 deficiency, Vitamin b12 deficiency, Vitamin b12
Children | Free Full-Text | Cystathionine Beta-Synthase Deficiency: Three Consecutive Cases Detected in 40 Days by Newborn Screening in Emilia Romagna (Italy) and a Comprehensive Review of the Literature
Protein Deficiency Learning Mat | Teaching Resources
DEFICIENCY? Serving size 1can 'Mat _14% Added Sugars _79% Alt source of nther autrients. source of ather sutrients: MEL Daily Value PROBLEM SOLVED - iFunny Brazil
Molecular genetics of hepatic methionine adenosyltransferase deficiency - ScienceDirect
