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 *

67 related articles for article (PubMed ID: 5557313)

  • 1. [Apropos of a case of cystathionuria with excretion of homocystine].
    Coignet J; Passeron P; Laurent B; Rouault F
    Pediatrie; 1971; 26(3):317-22. PubMed ID: 5557313
    [No Abstract]   [Full Text] [Related]  

  • 2. Homocystinuria: metabolism of [35S]methionine.
    Brenton DP; Cusworth DC
    Clin Sci; 1966 Oct; 31(2):197-206. PubMed ID: 5955721
    [No Abstract]   [Full Text] [Related]  

  • 3. [Cystathionuria and defective enzyme regulation].
    Laurent B; Coignet J
    Clin Chim Acta; 1973 Jan; 43(2):171-82. PubMed ID: 4687895
    [No Abstract]   [Full Text] [Related]  

  • 4. Aminoaciduria in a homocystinuric family.
    Kelly S; Copeland W; Leikhim E
    Clin Chim Acta; 1969 Dec; 26(3):586-7. PubMed ID: 5358562
    [No Abstract]   [Full Text] [Related]  

  • 5. Sulfur-containing amino acids in the plasma and urine of homocystinurics.
    Perry TL; Hansen S; MacDougall L; Warrington PD
    Clin Chim Acta; 1967 Mar; 15(3):409-20. PubMed ID: 6034417
    [No Abstract]   [Full Text] [Related]  

  • 6. Cystathioninuria in a well baby population.
    Lyon IC; Procopis PG; Turner B
    Acta Paediatr Scand; 1971 May; 60(3):324-8. PubMed ID: 5579857
    [No Abstract]   [Full Text] [Related]  

  • 7. Primary cystathioninuria. Methionine load tests and response to pyridoxine.
    Bremer HJ; Endres W
    Helv Paediatr Acta; 1972 Nov; 27(5):525-36. PubMed ID: 4640904
    [No Abstract]   [Full Text] [Related]  

  • 8. Effect of pyridoxine treatment of a cystathioninuric patient on the urinary excretion of some unusual sulfur-containing amino acids.
    Kodama H; Ikegami T; Hirayama K; Mizuhara S
    Clin Chim Acta; 1974 Feb; 51(1):29-34. PubMed ID: 4822813
    [No Abstract]   [Full Text] [Related]  

  • 9. [Hereditary tyrosinemia with hypermethioninemia. Study of the amino acids and keto acids].
    Vanheule R
    Verh K Acad Geneeskd Belg; 1973; 35(1):39-71. PubMed ID: 4730762
    [No Abstract]   [Full Text] [Related]  

  • 10. [Homocystinuria].
    Werder EA; Curtius HC; Tancredi F; Anders PW; Prader A
    Helv Paediatr Acta; 1966 Apr; 21(1):1-18. PubMed ID: 6010586
    [No Abstract]   [Full Text] [Related]  

  • 11. Further investigations in the methionine malabsorption syndrome.
    Hooft C; Carton D; Snoeck J; Timmermans J; Antener I; van den Hende C
    Helv Paediatr Acta; 1968 Aug; 23(4):334-49. PubMed ID: 5678411
    [No Abstract]   [Full Text] [Related]  

  • 12. [Changes of urinary excretion of orotic acid in a patient with ornithine carbamyl transferase deficiency].
    Sakane Y; Sugimoto T
    Rinsho Byori; 1982 May; 30(5):547-50. PubMed ID: 7131821
    [No Abstract]   [Full Text] [Related]  

  • 13. [Methionine malabsorption].
    Hooft C; Timmermans J; Snoeck J; Antener I; Oyaert W; Van den Hende C
    Verh K Vlaam Acad Geneeskd Belg; 1966; 28(1):15-39. PubMed ID: 5911135
    [No Abstract]   [Full Text] [Related]  

  • 14. [Methionine malabsorption].
    Pospísil R; Mrskos A; Srácková D; Hunka R; Habancová M
    Cas Lek Cesk; 1972; 111(8):178-81. PubMed ID: 5010327
    [No Abstract]   [Full Text] [Related]  

  • 15. Homocystinuria. II. Subnormal serum folate levels, increased folate clearance and effects of folic acid therapy.
    Carey MC; Fennelly JJ; FitzGerald O
    Am J Med; 1968 Jul; 45(1):26-31. PubMed ID: 5658866
    [No Abstract]   [Full Text] [Related]  

  • 16. Hyperargininaemia: a late-diagnosed Brazilian case with increased urinary excretion of homocystine.
    Simoni RE; de Oliveira CP; Braga MJ; de Menezes CR; Llerena Júnior JC; Correia PS; Rosa AA; Horovitz DG; Chaves CR; de Oliveira ML
    J Inherit Metab Dis; 1997 Sep; 20(5):715-6. PubMed ID: 9323573
    [No Abstract]   [Full Text] [Related]  

  • 17. [Attempted clinical orientation in the diagnosis of amino acid metabolism disorders. I. Urinary symptoms, neuropsychic symptoms and ocular symtpoms].
    Boisse J
    Presse Med (1893); 1968 Apr; 76(19):903-6. PubMed ID: 5645352
    [No Abstract]   [Full Text] [Related]  

  • 18. Diet therapy for inborn errors of amino acid metabolism.
    Efron ML
    J Am Diet Assoc; 1967 Jul; 51(1):40-5. PubMed ID: 6027632
    [No Abstract]   [Full Text] [Related]  

  • 19. Homocystinuria.
    White HH; Thompson HL; Rowland LP; Cowen D; Araki S
    Trans Am Neurol Assoc; 1964; 89():24-7. PubMed ID: 5828517
    [No Abstract]   [Full Text] [Related]  

  • 20. [Dietary management of hereditary tyrosinemia. Apropos of 7 cases].
    Jehan P; Buchman M; Odièvre M
    Ann Pediatr (Paris); 1984 Jan; 31(1):33-40. PubMed ID: 6712098
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.