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S‐Adenosylhomocysteine hydrolase deficiency: A second patient, the younger brother of the index patient, and outcomes during therapy

Journal of inherited metabolic disease, 2005-12, Vol.28 (6), p.885-902

2005

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S‐Adenosylhomocysteine hydrolase deficiency in a 26‐year‐old man

Journal of inherited metabolic disease, 2006-08, Vol.29 (4), p.538-545

2006

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Homocysteine and its disulfide derivatives: a suggested consensus terminology

Arteriosclerosis, thrombosis, and vascular biology, 2000-07, Vol.20 (7), p.1704-1706

2000

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Glycine N‐methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia

Journal of inherited metabolic disease, 2001-07, Vol.24 (4), p.448-464

2001

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Glycine N‐methyltransferase deficiency: A new patient with a novel mutation

Journal of inherited metabolic disease, 2003-01, Vol.26 (8), p.745-759

2003

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Consensus nomenclature for the mammalian methionine adenosyltransferase genes and gene products

Trends in genetics, 1997-02, Vol.13 (2), p.51-52

1997

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Methionine transamination in patients with homocystinuria due to cystathionine β-synthase deficiency

Metabolism, clinical and experimental, 2000-08, Vol.49 (8), p.1071-1077

2000

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Methionine adenosyltransferase I/III deficiency : Novel mutations and clinical variations

American journal of human genetics, 2000-02, Vol.66 (2), p.347-355

2000

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Isolated persistent hypermethioninemia

American journal of human genetics, 1995-10, Vol.57 (4), p.882-892

1995

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Maternal methionine adenosyltransferase I/III deficiency: Reproductive outcomes in a woman with four pregnancies

Journal of inherited metabolic disease, 2003-01, Vol.26 (5), p.443-458

2003

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Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene

American journal of human genetics, 1997-03, Vol.60 (3), p.540-546

1997

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Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: Diagnosis in an expanded neonatal screening programme

Journal of inherited metabolic disease, 2008-12, Vol.31 (Suppl 2), p.233-239

2008

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Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutation

Journal of inherited metabolic disease, 2002-12, Vol.25 (8), p.661-671

2002

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Maternal γ-cystathionase deficiency: Absence of both teratogenic effects and pregnancy complications

American journal of obstetrics and gynecology, 1999-09, Vol.181 (3), p.753-755

1999

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Enzymes of phosphatidylcholine synthesis in Lemna, soybean, and carrot

Plant physiology (Bethesda), 1988-12, Vol.88 (4), p.1338-1348

1988

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Phosphatidylcholine synthesis. Differing patterns in soybean and carrot

Plant physiology (Bethesda), 1988-11, Vol.88 (3), p.854-861

1988

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The natural history of homocystinura due to cystathionine β-synthase deficiency

American journal of human genetics, 1985, Vol.37 (1), p.1-31

1985

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Quantitative Analysis of Pathways of Methionine Metabolism and Their Regulation in Lemna

Plant physiology (Bethesda), 1985-07, Vol.78 (3), p.555-560

1985

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Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency

The Journal of clinical investigation, 1996-08, Vol.98 (4), p.1021-1027

1996

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Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency

The Journal of clinical investigation, 1988-02, Vol.81 (2), p.390-397

1988

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Persistent hypermethioninaemia with dominant inheritance

Journal of inherited metabolic disease, 1992-03, Vol.15 (2), p.188-197

1992

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Isolated hypermethioninemia: Measurements of S-adenosylmethionine and choline

Metabolism, clinical and experimental, 2000-12, Vol.49 (12), p.1542-1547

2000

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Regulatory structure of the biosynthetic pathway for the aspartate family amino acids in Lemna paucicostata Hegelm. 6746, with special reference to the role of aspartokinase

Plant physiology (Bethesda), 1989-08, Vol.90 (4), p.1584-1599

1989

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Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activity

The Journal of biological chemistry, 2001-04, Vol.276 (17), p.13803-13809

2001

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Synthesis of methylated ethanolamine moieties: regulation by choline in soybean and carrot

Plant physiology (Bethesda), 1989-05, Vol.90 (1), p.306-310

1989

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S‐Adenosylhomocysteine hydrolase deficiency: A second patient, the younger brother of the index patient, and outcomes during therapy

S‐Adenosylhomocysteine hydrolase deficiency in a 26‐year‐old man

Homocysteine and its disulfide derivatives: a suggested consensus terminology

Glycine N‐methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia

Glycine N‐methyltransferase deficiency: A new patient with a novel mutation

Consensus nomenclature for the mammalian methionine adenosyltransferase genes and gene products

Methionine transamination in patients with homocystinuria due to cystathionine β-synthase deficiency

Methionine adenosyltransferase I/III deficiency : Novel mutations and clinical variations

Isolated persistent hypermethioninemia

Maternal methionine adenosyltransferase I/III deficiency: Reproductive outcomes in a woman with four pregnancies

Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene

Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: Diagnosis in an expanded neonatal screening programme

Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutation

Maternal γ-cystathionase deficiency: Absence of both teratogenic effects and pregnancy complications

Enzymes of phosphatidylcholine synthesis in Lemna, soybean, and carrot

Phosphatidylcholine synthesis. Differing patterns in soybean and carrot

The natural history of homocystinura due to cystathionine β-synthase deficiency

Quantitative Analysis of Pathways of Methionine Metabolism and Their Regulation in Lemna

Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency

Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency

Persistent hypermethioninaemia with dominant inheritance

Isolated hypermethioninemia: Measurements of S-adenosylmethionine and choline

Regulatory structure of the biosynthetic pathway for the aspartate family amino acids in Lemna paucicostata Hegelm. 6746, with special reference to the role of aspartokinase

Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activity

Synthesis of methylated ethanolamine moieties: regulation by choline in soybean and carrot

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