T Reade

VITAMIN D DEPENDENCY: AN INHERITED POSTNATAL SYNDROME WITH SECONDARY HYPERPARATHYROIDISM

C. Arnaud, R. Maijer, T Reade et al. · PEDIATRICS · 1970 · 85 citations

Nutrition, Vitamin D2, Medicine +13

Hypophosphatemic nonrachitic bone disease: An entity distinct from X‐linked hypophosphatemia in the renal defect, bone involvement, and inheritance

Charles R. Scriver, Wendy A. MacDonald, T Reade et al. · American Journal of Medical Genetics · 1977 · 77 citations

Renal Pathology, Parathyroid Disease, Nephrology +20

Prospective analysis and classification of patients with cystinuria identified in a newborn screening program

Paul Goodyer, Carol L. Clow, T Reade et al. · The Journal of Pediatrics · 1993 · 70 citations

Urology, Neonatology, Newborn Screening Program +7

X-linked hypophosphatemia: the mutant gene is expressed in teeth as well as in kidney.

E D Shields, C. R. Scriver, T Reade et al. · PubMed · 1990 · 56 citations

Autosomal hypophosphataemic bone disease responds to 1,25-(OH)2D3.

C. R. Scriver, T Reade, Fahed Halal et al. · Archives of Disease in Childhood · 1981 · 32 citations · Full text

Renal Pathology, Pathology, Serum Phosphorus +17