Selection of transplantation procedures and perioperative management in primary hyperoxaluria type 1
Latta, K, Jamieson, N V, Scheinman, J I, Schärer, K, Bensman, A, Cochat, P, Legendre, C, Ruder, H, de Pauw, L, Toussaint, C
Published in Nephrology, dialysis, transplantation (1995)
Published in Nephrology, dialysis, transplantation (1995)
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The effect of pyridoxine on oxalate dynamics in three cases of primary hyperoxaluria (with glycollic aciduria)
WATTS, R. W. E, VEALL, N, PURKISS, P, MANSELL, M. A, HAYWOOD, E. F
Published in Clinical science (1979) (01.07.1985)
Published in Clinical science (1979) (01.07.1985)
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Journal Article
D-2-hydroxyglutaric aciduria: case report and biochemical studies
Chalmers, R A, Lawson, A M, Watts, R W, Tavill, A S, Kamerling, J P, Hey, E, Ogilvie, D
Published in Journal of inherited metabolic disease (01.12.1980)
Published in Journal of inherited metabolic disease (01.12.1980)
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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
DANPURE, C. J, PURKISS, P, JENNINGS, P. R, WATTS, R. W. E
Published in Clinical science (1979) (01.05.1986)
Published in Clinical science (1979) (01.05.1986)
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Journal Article
Histopathological studies of the temporal bones in Hurler's disease [mucopolysaccharidosis (MPS) IH]
Friedmann, I, Spellacy, E, Crow, J, Watts, R W
Published in Journal of laryngology and otology (01.01.1985)
Published in Journal of laryngology and otology (01.01.1985)
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Neuropathological and clinical correlations in Hurler disease
Watts, R W, Spellacy, E, Adams, J H
Published in Journal of inherited metabolic disease (01.09.1986)
Published in Journal of inherited metabolic disease (01.09.1986)
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Anomalies in the assay of parathyroid hormone in normocalcaemic patients with renal stone disease
Ashby, J P, Loveridge, N, Brown, R C, Zanelli, J M, Rinsler, M G, Watts, R W
Published in Clinical endocrinology (Oxford) (01.08.1988)
Published in Clinical endocrinology (Oxford) (01.08.1988)
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Family studies of the Lesch-Nyhan syndrome: the use of a restriction fragment length polymorphism (RFLP) closely linked to the disease gene for carrier state and prenatal diagnosis
Gibbs, D A, Headhouse-Benson, C M, Watts, R W
Published in Journal of inherited metabolic disease (01.01.1986)
Published in Journal of inherited metabolic disease (01.01.1986)
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