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Characterization of a High-Affinity Galanin Receptor in the Rat Anterior Pituitary: Absence of Biological Effect and Reduced Membrane Binding of the Antagonist M15 Differentiate it From the Brain/Gut Receptor

Proceedings of the National Academy of Sciences - PNAS, 1993-05, Vol.90 (9), p.4231-4235

1993

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SUCCESSFUL TREATMENT OF PRIMARY HYPEROXALURIA TYPE I BY COMBINED HEPATIC AND RENAL TRANSPLANTATION

The Lancet (British edition), 1987-08, Vol.330 (8557), p.474-475

1987

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Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein

Human molecular genetics, 1993-12, Vol.2 (12), p.2109-2116

1993

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Oxalate dynamics and removal rates during haemodialysis and peritoneal dialysis in patients with primary hyperoxaluria and severe renal failure

Clinical science (1979), 1984-05, Vol.66 (5), p.591-597

1984

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Oxalate Metabolism in End-Stage Renal Disease: the Effect of Ascorbic Acid and Pyridoxine

Nephrology, dialysis, transplantation, 1988, Vol.3 (1), p.28-32

1988

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Sequential studies of oxalate dynamics in primary hyperoxaluria

Clinical science (1979), 1983-12, Vol.65 (6), p.627-633

1983

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3-Methylhistidine excretion as an index of myofibrillar protein catabolism in neuromuscular disease

Journal of neurology, neurosurgery and psychiatry, 1979-06, Vol.42 (6), p.536-541

1979

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Vitamin B12 neuropathy is not due to failure to methylate myelin basic protein

Journal of the neurological sciences, 1986, Vol.72 (1), p.113-117

1986

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Dietary treatment eliminates succinylacetone from the urine of a patient with tyrosinaemia type 1

European journal of pediatrics, 1990-06, Vol.149 (9), p.637-639

1990

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The effect of pyridoxine on oxalate dynamics in three cases of primary hyperoxaluria (with glycollic aciduria)

Clinical science (1979), 1985-07, Vol.69 (1), p.87-90

1985

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Increased myofibrillar protein catabolism in Duchenne muscular dystrophy measured by 3-methylhistidine excretion in the urine

Journal of neurology, neurosurgery and psychiatry, 1977-10, Vol.40 (10), p.979-981

1977

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Successful pregnancy in a renal transplant recipient with type I primary hyperoxaluria

Transplantation, 1990-04, Vol.49 (4), p.811-812

1990

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Mitochondrial damage and the subcellular distribution of 2-oxoglutarate:glyoxylate carboligase in normal human and rat liver and in the liver of a patient with primary hyperoxaluria type I

Clinical science (1979), 1986-05, Vol.70 (5), p.417-425

1986

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Twin siblings with a Reye's-like syndrome associated with an abnormal organic aciduria, hypoglycemia, diarrhea, and vomiting with close similarities to Jamaican vomiting sickness

Pediatric research, 1980-10, Vol.14 (10), p.1097-1103

1980

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Molecular identification of binding sites for calcitonin gene-related peptide (CGRP) and islet amyloid polypeptide (IAPP) in mammalian lung : species variation and binding of truncated CGRP and IAPP

Endocrinology (Philadelphia), 1993-11, Vol.133 (5), p.2351-2361

1993

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The subcellular metabolism of glyoxylate in primary hyperoxaluria type 1: The relationship between glycine production and oxalate overproduction

Journal of inherited metabolic disease, 1988-06, Vol.11 (S2), p.212-214

1988

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The effects of fetal energy depletion on amniotic fluid concentrations of amino acids, organic acids and related metabolites

Journal of inherited metabolic disease, 1988-03, Vol.11 (1), p.103-113

1988

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Screening for organic acidurias and amino acidopathies in newborns and children

Journal of inherited metabolic disease, 1980-12, Vol.3 (1), p.27-43

1980

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Studies on abnormal metabolic function in Reye's syndrome

Journal of inherited metabolic disease, 1987-06, Vol.10 (S2), p.263-265

1987

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Biochemical and clinical studies of Friedreich's ataxia

Journal of neurology, neurosurgery and psychiatry, 1981-07, Vol.44 (7), p.574-580

1981

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Renal transplantation in primary hyperoxaluria

Annals of the Academy of Medicine, Singapore, 1987-04, Vol.16 (2), p.337

1987

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Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case

Clinical genetics, 1980-09, Vol.18 (3), p.203-210

1980

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Ionic recognition by proton-ionizable lariat ethers and their polymers

Pure and applied chemistry, 1993-01, Vol.65 (3), p.399-402

1993

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Studies on the composition of urinary glycosaminoglycans and oligosaccharides in patients with mucopolysaccharidoses who were receiving fibroblast transplants

Clinica chimica acta, 1983-06, Vol.131 (1), p.109-121

1983

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SERUM METHIONINE AND HEPATIC ENZYME ACTIVITY IN ANAESTHETISTS EXPOSED TO NITROUS OXIDE

British journal of anaesthesia : BJA, 1982-06, Vol.54 (6), p.593-597

1982

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Characterization of a High-Affinity Galanin Receptor in the Rat Anterior Pituitary: Absence of Biological Effect and Reduced Membrane Binding of the Antagonist M15 Differentiate it From the Brain/Gut Receptor

SUCCESSFUL TREATMENT OF PRIMARY HYPEROXALURIA TYPE I BY COMBINED HEPATIC AND RENAL TRANSPLANTATION

Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein

Oxalate dynamics and removal rates during haemodialysis and peritoneal dialysis in patients with primary hyperoxaluria and severe renal failure

Oxalate Metabolism in End-Stage Renal Disease: the Effect of Ascorbic Acid and Pyridoxine

Sequential studies of oxalate dynamics in primary hyperoxaluria

3-Methylhistidine excretion as an index of myofibrillar protein catabolism in neuromuscular disease

Vitamin B12 neuropathy is not due to failure to methylate myelin basic protein

Dietary treatment eliminates succinylacetone from the urine of a patient with tyrosinaemia type 1

The effect of pyridoxine on oxalate dynamics in three cases of primary hyperoxaluria (with glycollic aciduria)

Increased myofibrillar protein catabolism in Duchenne muscular dystrophy measured by 3-methylhistidine excretion in the urine

Successful pregnancy in a renal transplant recipient with type I primary hyperoxaluria

Mitochondrial damage and the subcellular distribution of 2-oxoglutarate:glyoxylate carboligase in normal human and rat liver and in the liver of a patient with primary hyperoxaluria type I

Twin siblings with a Reye's-like syndrome associated with an abnormal organic aciduria, hypoglycemia, diarrhea, and vomiting with close similarities to Jamaican vomiting sickness

Molecular identification of binding sites for calcitonin gene-related peptide (CGRP) and islet amyloid polypeptide (IAPP) in mammalian lung : species variation and binding of truncated CGRP and IAPP

The subcellular metabolism of glyoxylate in primary hyperoxaluria type 1: The relationship between glycine production and oxalate overproduction

The effects of fetal energy depletion on amniotic fluid concentrations of amino acids, organic acids and related metabolites

Screening for organic acidurias and amino acidopathies in newborns and children

Studies on abnormal metabolic function in Reye's syndrome

Biochemical and clinical studies of Friedreich's ataxia

Renal transplantation in primary hyperoxaluria

Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case

Ionic recognition by proton-ionizable lariat ethers and their polymers

Studies on the composition of urinary glycosaminoglycans and oligosaccharides in patients with mucopolysaccharidoses who were receiving fibroblast transplants

SERUM METHIONINE AND HEPATIC ENZYME ACTIVITY IN ANAESTHETISTS EXPOSED TO NITROUS OXIDE

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