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42. 50 years ago in The Journal of Pediatrics: Tyrosinemia--an inborn error of tyrosine metabolism with cirrhosis of the liver and multiple renal defects. Andersson HC J Pediatr; 2015 Apr; 166(4):896. PubMed ID: 25819913 [No Abstract] [Full Text] [Related]
43. HOMOCYSTINURIA, AN ERROR IN THE METABOLISM OF METHIONINE. GERRITSEN T; WAISMAN HA Pediatrics; 1964 Mar; 33():413-20. PubMed ID: 14129086 [No Abstract] [Full Text] [Related]
44. Tubular disorders of acid-base and phosphate metabolism. Chan JC; Alon U Nephron; 1985; 40(3):257-79. PubMed ID: 2989716 [No Abstract] [Full Text] [Related]
45. [Changes in kidney function during liver cirrhosis]. Montini T; Bernardi P; Bonavita E; Allegro G G Clin Med; 1969 Apr; 50(4):323-49. PubMed ID: 4929565 [No Abstract] [Full Text] [Related]
46. [CYSTINURIA. PATHOPHYSIOLOGY FROM THE STANDPOINT OF THE MECHANISM OF AMINO ACID TRANSFER IN THE KIDNEY TUBULES]. ABE Y; FURUKAWA S; SUGITA M; MURAKAMI K Sogo Rinsho; 1963 Dec; 12():2331-9. PubMed ID: 14101467 [No Abstract] [Full Text] [Related]
47. [Debré-De Toni-Fanconi syndrome with glycogenosis of the liver]. Bauer B Klin Wochenschr; 1968 Mar; 46(6):317-28. PubMed ID: 5245557 [No Abstract] [Full Text] [Related]
48. Basic and clinical concepts related to vitamin D metabolism and action (second of two parts). Haussler MR; McCain TA N Engl J Med; 1977 Nov; 297(19):1041-50. PubMed ID: 333288 [No Abstract] [Full Text] [Related]
49. [On some aspects of renal tubule physiopathology in childhood]. Bottone E; Macchia PA; Baldini G; Bani E Minerva Pediatr; 1973 Jul; 25(25):1073-118. PubMed ID: 4356737 [No Abstract] [Full Text] [Related]
58. [Renal involvement in type I tyrosinemia]. Cochat P; Guibaud P; Baverel G Arch Pediatr; 1994 Apr; 1(4):417-8. PubMed ID: 7842099 [No Abstract] [Full Text] [Related]
59. [Vitamin D and its therapeutic use]. Fournier A; Sebert JL; Boudailliez B; Morinière P Ann Med Interne (Paris); 1985; 136(2):164-79. PubMed ID: 3000252 [No Abstract] [Full Text] [Related]
60. Effect of dietary treatment on the renal tubular function in a patient with hereditary tyrosinemia. Suzuki Y; Konda M; Imai I; Imamura H; Shimao S; Okaka T Int J Pediatr Nephrol; 1987; 8(3):171-6. PubMed ID: 3429140 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]