These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 1638758)

  • 1. An immunoreactive xanthine oxidase protein-possessing xanthinuria and her family.
    Yamamoto T; Moriwaki Y; Suda M; Takahashi S; Hada T; Nanahoshi M; Agbedana EO; Higashino K
    Clin Chim Acta; 1992 Jun; 208(1-2):93-8. PubMed ID: 1638758
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A xanthinuric family--the proposita having immunologically reactive xanthine oxidase but no xanthine oxidase activity.
    Yamamoto T; Moriwaki Y; Takahashi S; Hada T; Suda M; Imanishi H; Agbedana OE; Nanahoshi M; Higashino K
    Adv Exp Med Biol; 1991; 309A():369-72. PubMed ID: 1789246
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of a new point mutation in the human molybdenum cofactor sulferase gene that is responsible for xanthinuria type II.
    Yamamoto T; Moriwaki Y; Takahashi S; Tsutsumi Z; Tuneyoshi K; Matsui K; Cheng J; Hada T
    Metabolism; 2003 Nov; 52(11):1501-4. PubMed ID: 14624414
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [The total absence of xanthine oxidase activity. Apropos 2 cases of the nonfamilial incidence of xanthinuria].
    Sastre Pascual JF; Roca Villanueva B; Arenas Jiménez MD; Mengual Alarte MJ; Zamora Navarro S; Boronat Botella M; Arenas Adarve M
    An Med Interna; 1991 Apr; 8(4):181-4. PubMed ID: 1912172
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Demonstration of a combined deficiency of xanthine oxidase and aldehyde oxidase in xanthinuric patients not forming oxipurinol.
    Reiter S; Simmonds HA; Zöllner N; Braun SL; Knedel M
    Clin Chim Acta; 1990 Mar; 187(3):221-34. PubMed ID: 2323062
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Xanthine oxidase deficiency (hereditary xanthinuria), molybdenum cofactor deficiency].
    Sumi S; Wada Y
    Nihon Rinsho; 1996 Dec; 54(12):3333-6. PubMed ID: 8976115
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary xanthinuria presenting in infancy with nephrolithiasis.
    Carpenter TO; Lebowitz RL; Nelson D; Bauer S
    J Pediatr; 1986 Aug; 109(2):307-9. PubMed ID: 3755469
    [No Abstract]   [Full Text] [Related]  

  • 8. Decreased xanthine oxidase activities and increased urinary oxypurines in heterozygotes for hereditary xanthinuria.
    Kawachi M; Kono N; Mineo I; Yamada Y; Tarui S
    Clin Chim Acta; 1990 Apr; 188(2):137-46. PubMed ID: 2379312
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Xanthinuria (author's transl)].
    Cartier P; Perignon JL
    Nouv Presse Med; 1978 Apr; 7(16):1381-90. PubMed ID: 673672
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Study of urinary pyrazinamide metabolites and their action on the renal excretion of xanthine and hypoxanthine in a xanthinuric patient.
    Auscher C; Pasquier C; Pehuet P; Delbarre F
    Biomedicine; 1978 May; 28(2):129-33. PubMed ID: 667278
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Xanthinuria: an additional case with demonstration of xanthine oxidase deficiency.
    Sperling O; Liberman UA; Frank M; de Vries A
    Am J Clin Pathol; 1971 Mar; 55(3):351-4. PubMed ID: 5549903
    [No Abstract]   [Full Text] [Related]  

  • 12. Clinicobiochemical analysis of four cases of xanthine oxidase deficiency.
    Nishioka K; Yamanaka H; Nishina T; Hosoya T; Mikanagi K
    Adv Exp Med Biol; 1984; 165 Pt A():73-6. PubMed ID: 6547018
    [No Abstract]   [Full Text] [Related]  

  • 13. Xanthinuria and xanthine calculous pyonephrosis.
    Kenawi MM
    J R Coll Surg Edinb; 1976 Mar; 21(2):95-9. PubMed ID: 933094
    [No Abstract]   [Full Text] [Related]  

  • 14. [A new method for the determination of xanthine oxidase activity by high-performance liquid chromatography with electrochemical detection].
    Kojima T; Nishina T; Yamanaka H
    Rinsho Byori; 1992 Oct; 40(10):1096-100. PubMed ID: 1307615
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Three cases of hereditary xanthinuria: review of the literature (author's transl)].
    Temperville B; Godin M; Dubois D; Fillastre JP
    Sem Hop; 1979 Dec 8-15; 55(41-42):1899-902. PubMed ID: 231309
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Hypouricemia and xanthinuria. Observation of 3 cases].
    Morini PL; Bandinelli R; Curiel P
    Minerva Med; 1979 Mar; 70(12):873-8. PubMed ID: 431842
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Family study of hereditary xanthinuria--decreased duodenal xanthine oxidase activity and increased urinary excretion of xanthine and hypoxanthine in heterozygotes.
    Kawachi M; Kono N; Mineo I; Hara N; Himeno S; Yamada Y; Kiyokawa H; Yamasaki T; Wang YL; Kuwajima M
    Adv Exp Med Biol; 1989; 253A():93-6. PubMed ID: 2624237
    [No Abstract]   [Full Text] [Related]  

  • 18. [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]  

  • 19. A case of xanthinuria: a study on the metabolism of pyrazinamide and allopurinol.
    Yamamoto T; Kario K; Suda M; Moriwaki Y; Takahashi S; Higashino K
    Jpn J Med; 1991; 30(5):430-4. PubMed ID: 1803043
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 8.