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

[1]  M. Kinoshita,et al.  S-adenosylmethionine treatment in methionine adenosyltransferase deficiency, a case report. , 2012, Molecular genetics and metabolism.

[2]  S. Mudd.  Hypermethioninemias of genetic and non‐genetic origin: A review , 2011, American journal of medical genetics. Part C, Seminars in medical genetics.

[3]  Y. Chien,et al.  Enzymatic activity of methionine adenosyltransferase variants identified in patients with persistent hypermethioninemia. , 2010, Molecular genetics and metabolism.

[4]  I. Barić.  Inherited disorders in the conversion of methionine to homocysteine , 2009, Journal of Inherited Metabolic Disease.

[5]  M. I. Mora,et al.  Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: Diagnosis in an expanded neonatal screening programme , 2008, Journal of Inherited Metabolic Disease.

[6]  E. Puffenberger,et al.  Prevention of brain disease from severe 5,10-methylenetetrahydrofolate reductase deficiency. , 2007, Molecular genetics and metabolism.

[7]  B. Olgemöller,et al.  Methionine adenosyltransferase (MAT) I/III deficiency with concurrent hyperhomocysteinaemia: Two novel cases , 2005, Journal of Inherited Metabolic Disease.

[8]  M. Pomper,et al.  Characteristic MR imaging changes in severe hypermethioninemic states. , 2005, AJNR. American journal of neuroradiology.

[9]  A. Barkovich,et al.  Reversible white matter lesion in methionine adenosyltransferase I/III deficiency. , 2004, AJNR. American journal of neuroradiology.

[10]  V. Ramesh,et al.  Cerebral edema associated with betaine treatment in classical homocystinuria. , 2004, The Journal of pediatrics.

[11]  Gabino Sanchez-Perez,et al.  Methionine adenosyltransferase as a useful molecular systematics tool revealed by phylogenetic and structural analyses. , 2004, Journal of molecular biology.

[12]  F. Corrales,et al.  Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutation , 2003, Journal of Inherited Metabolic Disease.

[13]  E. Naughten,et al.  The intellectual abilities of early-treated individuals with pyridoxine-nonresponsive homocystinuria due to cystathionine β-synthase deficiency , 2001, Journal of Inherited Metabolic Disease.

[14]  L. Elsas,et al.  Cystathionine β‐synthase deficiency in Georgia (USA): Correlation of clinical and biochemical phenotype with genotype , 2003, Human mutation.

[15]  M. Pomper,et al.  Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap. , 2003, Molecular genetics and metabolism.

[16]  A. Briddon.  Homocysteine in the context of cobalamin metabolism and deficiency states , 2003, Amino Acids.

[17]  C. Steegborn,et al.  Elevated plasma total homocysteine in severe methionine adenosyltransferase I/III deficiency. , 2002, Metabolism: clinical and experimental.

[18]  M. Pomper,et al.  Progressive cerebral edema associated with high methionine levels and betaine therapy in a patient with cystathionine beta-synthase (CBS) deficiency. , 2002, American journal of medical genetics.

[19]  G. Boers,et al.  Vascular Outcome in Patients With Homocystinuria due to Cystathionine &bgr;-Synthase Deficiency Treated Chronically: A Multicenter Observational Study , 2001, Arteriosclerosis, thrombosis, and vascular biology.

[20]  D. Jenden,et al.  Isolated hypermethioninemia: measurements of S-adenosylmethionine and choline. , 2000, Metabolism: clinical and experimental.

[21]  J. Chou,et al.  Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations. , 2000, American journal of human genetics.

[22]  M. Kotb,et al.  Consensus nomenclature for the mammalian methionine adenosyltransferase genes and gene products. , 1997, Trends in Genetics.

[23]  J. Leonard,et al.  Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency. , 1996, The Journal of clinical investigation.

[24]  H. Levy,et al.  Isolated persistent hypermethioninemia. , 1995, American journal of human genetics.

[25]  J. Chou,et al.  Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency. , 1995, The Journal of clinical investigation.

[26]  R. Surtees,et al.  Association of demyelination with deficiency of cerebrospinal-fluid S-adenosylmethionine in inborn errors of methyl-transfer pathway , 1991, The Lancet.

[27]  K. Ishak,et al.  Hepatic methionine adenosyltransferase deficiency in a 31-year-old man. , 1987, American journal of human genetics.

[28]  K. Pettigrew,et al.  The natural history of homocystinuria due to cystathionine beta-synthase deficiency. , 1985, American journal of human genetics.