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 *

197 related articles for article (PubMed ID: 701680)

  • 21. Tyrosinemia type III: diagnosis and ten-year follow-up.
    Cerone R; Holme E; Schiaffino MC; Caruso U; Maritano L; Romano C
    Acta Paediatr; 1997 Sep; 86(9):1013-5. PubMed ID: 9343288
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Dietary treatment eliminates succinylacetone from the urine of a patient with tyrosinaemia type 1.
    Bain MD; Purkiss P; Jones M; Bingham P; Stacey TE; Chalmers RA
    Eur J Pediatr; 1990 Jun; 149(9):637-9. PubMed ID: 2373116
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A new variant form of hypertyrosinaemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency.
    Endo F; Kitano A; Uehara I; Nagata N; Matsuda I; Shinka T; Kuhara T; Matsumoto I
    J Inherit Metab Dis; 1982; 5(4):237-8. PubMed ID: 6133038
    [No Abstract]   [Full Text] [Related]  

  • 24. [Sepsis, as the presenting form of hereditary tyrosinemia type I].
    Iglesias Niubo J; Riudor Taravilla E; Goma Brufau AR; Civit Colas MA; Suñé Gracia JM; Bertrán Sanges JM; Gallart Catalá A
    An Esp Pediatr; 1988 Sep; 29(3):235-8. PubMed ID: 3057981
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Biochemical observations on so-called hereditary tyrosinemia.
    Gaull GE; Rassin DK; Solomon GE; Harris RC; Sturman JA
    Pediatr Res; 1970 Jul; 4(4):337-44. PubMed ID: 4393588
    [No Abstract]   [Full Text] [Related]  

  • 26. Phenylalanine-tyrosine deficiency syndrome as a complication of the management of hereditary tyrosinemia.
    Cohn RM; Yudkoff M; Yost B; Segal S
    Am J Clin Nutr; 1977 Feb; 30(2):209-14. PubMed ID: 835507
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Determination of branched chain amino acids, methionine, phenylalanine, tyrosine and alpha-keto acids in plasma and dried blood samples using HPLC with fluorescence detection.
    Kand'ár R; Záková P; Jirosová J; Sladká M
    Clin Chem Lab Med; 2009; 47(5):565-72. PubMed ID: 19290779
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Tyrosinemia associated with hypermethioninemia and islet cell hyperplasia.
    Perry TL
    Can Med Assoc J; 1967 Oct; 97(18):1067-75. PubMed ID: 4862180
    [No Abstract]   [Full Text] [Related]  

  • 29. Chronic tyrosinemia associated with 4-hydroxyphenylpyruvate dioxygenase deficiency with acute intermittent ataxia and without visceral and bone involvement.
    Giardini O; Cantani A; Kennaway NG; D'Eufemia P
    Pediatr Res; 1983 Jan; 17(1):25-9. PubMed ID: 6132360
    [No Abstract]   [Full Text] [Related]  

  • 30. American Academy of Pediatrics. Committee on Nutrition: special diets for infants with inborn errors of amino acid metabolism.
    Pediatrics; 1976 May; 57(5):783-92. PubMed ID: 940719
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Biochemical study of malnutrition. Part V. Metabolism of phenylalanine and tyrosine.
    Antener I; Verwilghen AM; van Geert C; Mauron J
    Int J Vitam Nutr Res; 1981; 51(3):297-306. PubMed ID: 6119298
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Metabolic studies on two patients with nonhepatic tyrosinemia using deuterated tyrosine loads.
    Faull KF; Gan I; Halpern B; Hammond J; Im S; Cotton RG; Danks DM; Freeman R
    Pediatr Res; 1977 May; 11(5):631-7. PubMed ID: 870870
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Urinary p-tyramine in hereditary tyrosinemia: II. Origin of urinary p-tyramine.
    Hoag GN; Hill A; Zaleski W
    Clin Biochem; 1977 Feb; 10(1):26-8. PubMed ID: 837523
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Parahydroxyphenylpyruvicacidemia in tyrosinosis.
    Jaiswal RB; Bhai I; Daginawala HF; Nath N; Nath MC
    Indian Pediatr; 1978 Nov; 15(11):893-9. PubMed ID: 36347
    [No Abstract]   [Full Text] [Related]  

  • 35. A new form of prolonged transient tyrosinemia presenting with severe metabolic acidosis.
    Danks DM; Tippett P; Rogers J
    Acta Paediatr Scand; 1975 Mar; 64(2):209-14. PubMed ID: 1130176
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuria.
    Tomoeda K; Awata H; Matsuura T; Matsuda I; Ploechl E; Milovac T; Boneh A; Scott CR; Danks DM; Endo F
    Mol Genet Metab; 2000 Nov; 71(3):506-10. PubMed ID: 11073718
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [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]  

  • 38. Cholestasis and hypermethioninemia during dietary management of hereditary tyrosinemia type 1.
    Ameen VZ; Powell GK; Rassin DK
    J Pediatr; 1986 Jun; 108(6):949-52. PubMed ID: 2872285
    [No Abstract]   [Full Text] [Related]  

  • 39. The dietary management of inborn errors of metabolism.
    Collins JE; Leonard JV
    Hum Nutr Appl Nutr; 1985 Aug; 39(4):255-72. PubMed ID: 3900002
    [TBL] [Abstract][Full Text] [Related]  

  • 40. High protein diet mimics hypertyrosinemia in newborn infants.
    Techakittiroj C; Cunningham A; Hooper PF; Andersson HC; Thoene J
    J Pediatr; 2005 Feb; 146(2):281-2. PubMed ID: 15689925
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.