Alkaptonuria: a 60-yr follow-up von Watts, R. W. E., Watts, R. A.

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Idiopathic urinary stone disease: possible polygenic aetiological factors von Watts, R W E

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Combined Liver–Kidney and Isolated Liver Transplantations for Primary Hyperoxaluria Type 1: The European Experience von Watts, R. W. E., Danpure, C. J., De Pauw, L., Toussaint, C.

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Selection of transplantation procedures and perioperative management in primary hyperoxaluria type 1 von LATTA, K, JAMIESON, N. V, WATTS, R. W. E, MANSELL, M. A, SCHEINMAN, J. I, SCHÄRER, K, BENSMAN, A, COCHAT, P, LEGENDRE, C, RUDER, H, DE PAUW, L, TOUSSAINT, C

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The quantitative extraction and gas-liquid chromatographic determination of organic acids in urine von Chalmers, R A, Watts, R W

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Oxalate Metabolism in End-Stage Renal Disease: the Effect of Ascorbic Acid and Pyridoxine von Morgan, S. H., Maher, E. R., Purkiss, P., Watts, R. W. E., Curtis, J. R.

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Molecular variation in relation to purine metabolism von Watts, R. W. E.

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Lesch‐Nyhan syndrome and its pathogenesis: Purine concentrations in plasma and urine with metabolite profiles in CSF von Harkness, R. A., McCreanor, G. M., Watts, R. W. E.

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D‐2‐hydroxyglutaric aciduria: Case report and biochemical studies von Chalmers, R. A., Lawson, A. M., Watts, R. W. E., Tavill, A. S., Kamerling, J. P., Hey, E., Ogilvie, D.

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Lesch‐nyhan syndrome: Growth delay, testicular atrophy and a partial failure of the 11β‐hydroxylation of steroids von Watts, R. W. E., Harkness, R. A., Spellacy, E., Taylor, N. F.

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Histopathological studies of the temporal bones in Hurler's disease [Mucopolysaccharidosis (MPS) IH] von Friedmann, I., Spellacy, Elizabeth, Crow, Julie, Watts, R. W. E.

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Neuropathological and clinical correlations in hurler disease von Watts, R. W. E., Spellacy, E., Hume Adams, J.

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Primary hyperoxaluria type I von Watts, R W

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Selective renal transplantation in primary hyperoxaluria type 1 von Allen, A.R., Thompson, E.M., Williams, G., Watts, R.W.E., Pusey, C.D.

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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... von Gibbs, D. A., Headhouse‐Benson, C. M., Watts, R. W. E.

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Screening for organic acidurias and amino acidopathies in newborns and children von Chalmers, R. A., Purkiss, P., Watts, R. W. E., Lawson, A. M.

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The third workshop on primary hyperoxaluria von Watts, R. W. E.

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Metabolic yearbook von Watts, R. W. E

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Amniotic fluid von Watts, R. W. E

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SUCCESSFUL TREATMENT OF PRIMARY HYPEROXALURIA TYPE I BY COMBINED HEPATIC AND RENAL TRANSPLANTATION von Watts, R.W.E., Rolles, K., Morgan, S.H., Williams, Roger, Calne, R.Y., Danpure, C.J., Mansell, M.A., Purkiss, P.

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