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- W2038693443 abstract "A patient with Wilson9s disease presented at the age of 41 with a neurological defect and gross osteomalacia secondary to a defect of renal tubular reabsorption. He also showed the unusual features of a renal stone in the presence of the Fanconi syndrome and a relatively low alkaline phosphatase level, possibly due to the additional inherited defect of hypophosphatasia. During four years of treatment with penicillamine and calciferol clinical improvement was spectacular. Details of amino-acid clearances before and after treatment are given, and the results suggest that, as in the brain and the liver, the function of the distal renal tubules may be restored in Wilson9s disease when copper is removed." @default.
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- W2038693443 date "1961-04-01" @default.
- W2038693443 modified "2023-09-26" @default.
- W2038693443 title "Congenital Thrombocytopenic Purpura Treated by Exchange Transfusion" @default.
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- W2038693443 doi "https://doi.org/10.1136/adc.36.186.210" @default.
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