Mudd’s disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes

Neurologically normal development of a patient with severe methionine adenosyltransferase I/III deficiency after continuing dietary methionine restriction

(2013) Koichi Hirabayashi et al.   GENE

Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening

(2013) María L. Couce et al.   MOLECULAR GENETICS AND METABOLISM

Methionine adenosyltransferase I/III deficiency: Neurological manifestations and relevance of S-adenosylmethionine

(2012) Mahoko Furujo et al.   MOLECULAR GENETICS AND METABOLISM

Hypermethioninemias of genetic and non-genetic origin: A review

(2011) S. Harvey Mudd   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

S-adenosylmethionine treatment in methionine adenosyltransferase deficiency, a case report

(2011) Mahoko Furujo et al.   MOLECULAR GENETICS AND METABOLISM

The biochemical and toxicological significance of hypermethionemia: new insights and clinical relevance

(2010) Joseph T Dever et al.   Expert Opinion on Drug Metabolism & Toxicology

Uncovering the Human Methyltransferasome

(2010) Tanya C. Petrossian et al.   MOLECULAR & CELLULAR PROTEOMICS

Enzymatic activity of methionine adenosyltransferase variants identified in patients with persistent hypermethioninemia

(2010) Joaquín Fernández-Irigoyen et al.   MOLECULAR GENETICS AND METABOLISM

Pathogenesis of Cobalamin Neuropathy: Deficiency of Nervous System S-Adenosylmethionine?

(2010) Jack Metz   NUTRITION REVIEWS

Conformational signals in the C-terminal domain of methionine adenosyltransferase I/III determine its nucleocytoplasmic distribution

(2009) Edel Reytor et al.   FASEB JOURNAL

Dietary Docosahexaenoic Acid Supplementation Modulates Hippocampal Development in thePemt−/−Mouse

(2009) Kerry-Ann da Costa et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population

(2009) Erin M. Coffee et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Pathogenesis of cognitive dysfunction in phenylketonuria: Review of hypotheses☆

(2009) M.J. de Groot et al.   MOLECULAR GENETICS AND METABOLISM

Dietary omega 3 fatty acids and the developing brain

(2008) Sheila M. Innis   BRAIN RESEARCH

The Radical SAM Superfamily

(2008) Perry A. Frey et al.   CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY