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2. Pathogenesis of hereditary vitamin-D-dependent rickets. An inborn error of vitamin D metabolism involving defective conversion of 25-hydroxyvitamin D to 1 alpha,25-dihydroxyvitamin D. Fraser D, Kooh SW, Kind HP, Holick MF, Tanaka Y, DeLuca HF. N Engl J Med; 1973 Oct 18; 289(16):817-22. PubMed ID: 4357855 [No Abstract] [Full Text] [Related]
3. Familial hypophosphatemia: the dilemma of treatment. Scriver CR. N Engl J Med; 1973 Sep 06; 289(10):531-2. PubMed ID: 4353219 [No Abstract] [Full Text] [Related]
4. New developments in pharmacology of vitamin D. Med Lett Drugs Ther; 1974 Feb 01; 16(3):15-6. PubMed ID: 4358446 [No Abstract] [Full Text] [Related]
5. Familial hypophosphatemic rickets: a delineation of its subdivisions and pathogenesis. Walton J. Clin Pediatr (Phila); 1976 Nov 01; 15(11):1007-12. PubMed ID: 184998 [No Abstract] [Full Text] [Related]
6. [Vitamin D and its therapeutic use]. Fournier A, Sebert JL, Boudailliez B, Morinière P. Ann Med Interne (Paris); 1985 Nov 01; 136(2):164-79. PubMed ID: 3000252 [No Abstract] [Full Text] [Related]
19. [Scriver type autosomal hypophosphatemic rachitis: a family case]. David L, Pesso JL, Cochat P, Plauchu H, François R. Pediatrie; 1987 Dec 01; 42(7):563-8. PubMed ID: 2832821 [Abstract] [Full Text] [Related]
20. Nature of defect responsible for familial vitamin D-resistant rickets (VDRR) based on radioimmunoassay for parathyroid hormone (PTH). Roof BS, Piel CF, Gordan GS. Trans Assoc Am Physicians; 1972 Dec 01; 85():172-80. PubMed ID: 4349621 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]