FURTHER OBSERVATIONS ON USE OF D-PENICILLAMINE IN CYSTINURIA.
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Adolescent↗
Biomedical subjects
R W WATTS
Publications and source records attributed to R W WATTS.
ENZYME DEFECT IN A CASE OF XANTHINURIA.
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Biopsy↗
CLINICAL, PHYSIOLOGICAL AND BIOCHEMICAL STUDIES OF A PATIENT WITH XANTHINURIA AND PHEOCHROMOCYTOMA.
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Blood↗
QUANTITATIVE ASPECTS OF ASCORBIC ACID METABOLISM IN MAN.
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Ascorbic Acid↗
PRIMARY HYPEROXALURIA. THE RELATION BETWEEN ASCORBIC ACID AND THE INCREASED URINARY EXCRETION OF OXALATE.
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Ascorbic Acid↗
Effect of penicillamine on cystinuria.
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Chelating Agents↗
Congenital abnormalities of amino-acid metabolism.
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Amino Acids↗
The mechanism of the renal excretion of oxalate in the dog.
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Animals↗
The oxalate content of human plasma.
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Humans↗
Acylative decarboxylation with particular reference to the acetylative decarboxylation of the 2:4-dinitrophenyl derivatives of some amino acids.
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Amino Acids↗
Clinical manifestations of primary hyperoxaluria.
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Humans↗
A survey of some hereditary metabolic diseases.
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Data Collection↗
Conversion of glycine to oxalate in primary hyperoxaluria.
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Glycine↗
Conversion of glycine to oxalate in a normal subject.
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Glycine↗
The first glycine metabolic pool in man.
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Glycine↗
Further observations on the genetic basis of primary hyperoxaluria.
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Humans↗
A study of cases manifesting low voltage in the frontal plane electrocardiographic leads.
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Electrocardiography↗