169 related articles for article (PubMed ID: 196272)
41. 2,8-Dihydroxyadeninuria--or when is a uric acid stone not a uric acid stone?
Simmonds HA
Clin Nephrol; 1979 Nov; 12(5):195-7. PubMed ID: 389507
[No Abstract] [Full Text] [Related]
42. Study of purine metabolism in a xanthinuric female.
Bradford MJ; Krakoff IH; Leeper R; Balis ME
J Clin Invest; 1968 Jun; 47(6):1325-32. PubMed ID: 5653212
[TBL] [Abstract][Full Text] [Related]
43. [Xanthinuria].
Berger R; Broyer M
Presse Med (1893); 1968 Mar; 76(11):522. PubMed ID: 5646257
[No Abstract] [Full Text] [Related]
44. [Determination of oxypurine and its clinical implication].
Hisatome I; Kotake H; Mashiba H
Nihon Rinsho; 1989 Dec; 48 Suppl():413-6. PubMed ID: 2560080
[No Abstract] [Full Text] [Related]
45. [Hyperuricemia due to hypoxanthine-guanine-phosphoribosyltransferase deficiency].
Blétry O; Cartier P; Hamet M; Clauvel JP
Nouv Presse Med; 1974 Apr; 3(16):995-9. PubMed ID: 4836472
[No Abstract] [Full Text] [Related]
46. [Female gout in the fertile age].
Carcassi A
Reumatismo; 1977; 29(2-3):101-4. PubMed ID: 212801
[No Abstract] [Full Text] [Related]
47. Metabolic aspects in gout.
Alvsaker JO
Scand J Rheumatol Suppl; 1984; 53():54-63. PubMed ID: 6330884
[No Abstract] [Full Text] [Related]
48. Alterations of human purine metabolism in megaloblastic anemia.
Fox IH; Dotten DA; Marchant PJ
Adv Exp Med Biol; 1977; 76B():249-55. PubMed ID: 193381
[No Abstract] [Full Text] [Related]
49. Disorders associated with hyperuricemia.
Smyth CJ
Arthritis Rheum; 1975; 18(6 Suppl):713-9. PubMed ID: 173348
[No Abstract] [Full Text] [Related]
50. [Idiopathic hyperuricemia].
Fujimori S
Nihon Rinsho; 2003 Jan; 61 Suppl 1():172-7. PubMed ID: 12629713
[No Abstract] [Full Text] [Related]
51. Overproduction of uric acid in primary gout.
Yü TF; Balis ME; Yip LC
Arthritis Rheum; 1975; 18(6 Suppl):695-8. PubMed ID: 173347
[No Abstract] [Full Text] [Related]
52. [Hereditary xanthinuria. A clinical case report].
Pessano B; Davì S; La Brocca A; Leone L
Minerva Med; 1989 May; 80(5):507-9. PubMed ID: 2747979
[TBL] [Abstract][Full Text] [Related]
53. Primary hyperoxaluria, treated with haemodialysis and kidney transplantation.
Jacobsen E; Mosbaek N
Dan Med Bull; 1974 Apr; 21(2):72-6. PubMed ID: 4598252
[No Abstract] [Full Text] [Related]
54. Findings in kidney stone patients. Metabolic and clinical anomalies. Experience in Greece.
Kallistratos G; Marketos S; Lapatzanis P; Demopoulos K
Scand J Urol Nephrol Suppl; 1980; 53():195-7. PubMed ID: 6937996
[No Abstract] [Full Text] [Related]
55. Hereditary xanthinuria: report of two cases.
Chu TS
J Formos Med Assoc; 1993 May; 92(5):478-81. PubMed ID: 8104605
[TBL] [Abstract][Full Text] [Related]
56. Partial hypoxanthine-guanine phosphoribosyl transferase deficiency without elevated urinary hypoxanthine excretion.
van Dael CM; Pierik LJ; Reijngoud DJ; Niezen-Koning KE; van Diggelen OP; van Spronsen FJ
Mol Genet Metab; 2007 Feb; 90(2):221-3. PubMed ID: 17129743
[TBL] [Abstract][Full Text] [Related]
57. [Familial xanthinuria, 2 new cases].
Pereg Macazaga V; García Fernández H; Regúlez M; Elorza Olabegoya JR; Beitia Martín JJ; Vázquez García JA
Med Clin (Barc); 1984 Mar; 82(8):364-5. PubMed ID: 6546962
[No Abstract] [Full Text] [Related]
58. [Hyperuricemia associated with inborn errors of purine metabolism: screening, enzymatic and genetic diagnosis].
Yamada Y
Nihon Rinsho; 2003 Jan; 61 Suppl 1():278-83. PubMed ID: 12629731
[No Abstract] [Full Text] [Related]
59. Efficacy and safety of allopurinol in patients with hypoxanthine-guanine phosphoribosyltransferase deficiency.
Torres RJ; Prior C; Puig JG
Metabolism; 2007 Sep; 56(9):1179-86. PubMed ID: 17697859
[TBL] [Abstract][Full Text] [Related]
60. Adenine phosphoribosyltransferase deficiency as a rare cause of renal allograft dysfunction.
Kaartinen K; Hemmilä U; Salmela K; Räisänen-Sokolowski A; Kouri T; Mäkelä S
J Am Soc Nephrol; 2014 Apr; 25(4):671-4. PubMed ID: 24459232
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
