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Hydrolysis and transport of proline-containing peptides in renal brush-border membrane vesicles from dipeptidyl peptidase IV-positive and dipeptidyl peptidase IV-negative rat strains

The Journal of biological chemistry, 1990-01, Vol.265 (3), p.1476-1483

1990

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Kearns-Sayre syndrome and complex II deficiency

Neurology, 1989-05, Vol.39 (5), p.693-693

1989

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Adult-onset chorea and dementia with propionic acidemia

Neurology, 1989-10, Vol.39 (10), p.1343-1343

1989

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HPLC assay of phenylalanine and tyrosine in blood spots on filter paper

Clinica chimica acta, 1986-04, Vol.156 (1), p.91-96

1986

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Biochemical observations on a case of hepatic fructose‐1,6‐diphosphatase deficiency

Journal of inherited metabolic disease, 1985-12, Vol.8 (4), p.169-173

1985

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Dyggve‐Melchior‐Clausen syndrome with increased pipecolic acid in plasma and urine

Journal of inherited metabolic disease, 1991-11, Vol.14 (6), p.876-880

1991

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Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)

Neuropediatrics, 1986-02, Vol.17 (1), p.48-52

1986

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Increased excretion of histidyl-L-proline diketopiperazine by infants receiving Pregestimil and Nutramigen formulas

Clinical chemistry (Baltimore, Md.), 1986-05, Vol.32 (5), p.865-867

1986

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Combined xanthine and sulphite oxidase defect due to a deficiency of molybdenum cofactor

Journal of inherited metabolic disease, 1986-12, Vol.9 (4), p.343-347

1986

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Interaction of proline, 5-oxoproline, and pipecolic acid for renal transport in the rabbit

The Journal of biological chemistry, 1983-02, Vol.258 (4), p.2266-2272

1983

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γ-Glutamylornithine excretion in patients with hyperornithinemia

Clinica chimica acta, 1984-07, Vol.140 (2), p.133-138

1984

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5‐Hydroxy‐L‐lysine excretion in cystinuria

Journal of inherited metabolic disease, 1985-09, Vol.8 (3), p.123-126

1985

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Lactic, levulinic, and crotonic acids as artifacts in hydrolyzed urine

Clinical chemistry (Baltimore, Md.), 1979-01, Vol.25 (1), p.193-194

1979

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Serum carnosinase deficiency: a non-disabling phenotype?

Journal of mental deficiency research, 1985-12, Vol.29 ( Pt 4), p.383

1985

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Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia

Journal of inherited metabolic disease, 1982-03, Vol.5 (1), p.41-47

1982

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Transport of 5-oxoproline into rabbit renal brush border membrane vesicles

Biochemical and biophysical research communications, 1982-03, Vol.105 (1), p.28-35

1982

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Infantile free sialuria without lysosomal storage

Pediatric neurology, 1987, Vol.3 (1), p.40-43

1987

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Update on the Male and Female Climacteric

Journal of the American Geriatrics Society (JAGS), 1979-11, Vol.27 (11), p.481-490

1979

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Hydroxyproline metabolism in two sisters with hydroxyprolinemia

Human heredity, 1979, Vol.29 (6), p.364-370

1979

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Collagen synthesis by cloned mouse mammary tumor cells

Cancer research (Chicago, Ill.), 1978-10, Vol.38 (10), p.3269-3275

1978

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Determination of cystine excretion by the nitroprusside method during drug therapy of cystinuria

Clinica chimica acta, 1974-05, Vol.52 (3), p.343-346

1974

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Interference by methenamine mandelate in screening for organic and amino acid disorders

Clinica chimica acta, 1980, Vol.100 (1), p.55-58

1980

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Serum carnosinase deficiency: Decreased affinity of the enzyme for the substrate

Journal of inherited metabolic disease, 1982-03, Vol.5 (S1), p.13-14

1982

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Interference by meglumine diatrizoate in screening for amino-acid disorders

Clinica chimica acta, 1978-01, Vol.83 (3), p.293-294

1978

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Loss of transferase enzyme activity of transfused erythrocytes in galactosemia

Southern medical journal (Birmingham, Ala.), 1975-03, Vol.68 (3), p.301-302

1975

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Hydrolysis and transport of proline-containing peptides in renal brush-border membrane vesicles from dipeptidyl peptidase IV-positive and dipeptidyl peptidase IV-negative rat strains

Kearns-Sayre syndrome and complex II deficiency

Adult-onset chorea and dementia with propionic acidemia

HPLC assay of phenylalanine and tyrosine in blood spots on filter paper

Biochemical observations on a case of hepatic fructose‐1,6‐diphosphatase deficiency

Dyggve‐Melchior‐Clausen syndrome with increased pipecolic acid in plasma and urine

Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)

Increased excretion of histidyl-L-proline diketopiperazine by infants receiving Pregestimil and Nutramigen formulas

Combined xanthine and sulphite oxidase defect due to a deficiency of molybdenum cofactor

Interaction of proline, 5-oxoproline, and pipecolic acid for renal transport in the rabbit

γ-Glutamylornithine excretion in patients with hyperornithinemia

5‐Hydroxy‐L‐lysine excretion in cystinuria

Lactic, levulinic, and crotonic acids as artifacts in hydrolyzed urine

Serum carnosinase deficiency: a non-disabling phenotype?

Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia

Transport of 5-oxoproline into rabbit renal brush border membrane vesicles

Infantile free sialuria without lysosomal storage

Update on the Male and Female Climacteric

Hydroxyproline metabolism in two sisters with hydroxyprolinemia

Collagen synthesis by cloned mouse mammary tumor cells

Determination of cystine excretion by the nitroprusside method during drug therapy of cystinuria

Interference by methenamine mandelate in screening for organic and amino acid disorders

Serum carnosinase deficiency: Decreased affinity of the enzyme for the substrate

Interference by meglumine diatrizoate in screening for amino-acid disorders

Loss of transferase enzyme activity of transfused erythrocytes in galactosemia

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