Calcium Disorders by David Heath and Stephen J. Marx (Eds.)

By David Heath and Stephen J. Marx (Eds.)

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Acta 28, 247-270 (1941) Paediatrica, 25 CLOW, c. , READE, T. M. a n d SCRIVER, c. R. M a n a g e m e n t of h e r e d i t a r y m e t a b o l i c disease: t h e role of allied health personnel. , MARIE, P. , SCRIVER, C. , COLE, D. E. C , READE, T. , G L O R I E U X , F. H. a n d DELViN, E. E. X - l i n k e d h y p o p h o s p h a t e m i a : effect of calcitriol on renal handling of phosphate serum phosphate and bone mineralization. Journal of Clinical Endocrinology and Metabolism, 54, 463-476 (1981) 27 cowGiLL, L.

LESTER, G. E. a n d LORENC, R. s. E v i d e n c e f o r e x t r a - r e n a l l a hydroxylation of 25-hydroxyvitamin D 3 in pregnancy. Science, 204, 1311-1313 (1979) 66 G R E E N B E R G , B. , WINTERS, R. w. a n d G R A H A M , J. B. T h e n o r m a l r a n g e s of s e r u m inorganic phosphorus and its utility as a discriminant in the diagnosis of congenital hypophosphatemia. Journal of Clinical Endocrinology and Metabolism, 20, 364 (1960) 67 GRIFFITH, E. , PONNAMPERUMA, c. a n d GABEL, N.

Such a hypothesis is of interest primarily for the experiments it suggests in the Hyp mouse and as a source of insight regarding the mechanisms of rickets in phosphopenic states. Autosomal dominant hypophosphatemic rickets (ADHR) Harrison and Harrison73 described a phenotype strongly resembling X-linked hypophosphatemia in its severity that was dominantly inherited yet clearly autosomal in linkage. Insufficient experimental data are offered73 to discern how this condition might differ from both X-linked hypophosphatemia and hypophosphatemic bone disease in renal handling of the phosphate.

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