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 *

404 related articles for article (PubMed ID: 4697972)

  • 21. Dietary restriction in inborn errors of amino acid metabolism.
    Bickel H
    Curr Concepts Nutr; 1979; 8():35-53. PubMed ID: 527358
    [No Abstract]   [Full Text] [Related]  

  • 22. Transport of amino acids and peptides in the gut and the kidney.
    Milne MD
    Sci Basis Med Annu Rev; 1971; ():161-77. PubMed ID: 4933913
    [No Abstract]   [Full Text] [Related]  

  • 23. Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study.
    Humangenetik; 1975 Dec; 30(4):273-86. PubMed ID: 1218857
    [No Abstract]   [Full Text] [Related]  

  • 24. Disorders of amino acid metabolism--1971.
    Menkes JH
    Calif Med; 1971 Oct; 115(4):14-23. PubMed ID: 5110588
    [No Abstract]   [Full Text] [Related]  

  • 25. [Eye manifestations of amino acid disorders].
    Greco GM; Magli A
    Minerva Pediatr; 1978 May; 30(10):761-80. PubMed ID: 353484
    [No Abstract]   [Full Text] [Related]  

  • 26. Inherited disorders of amino acid transport in relation to the kidney.
    Buehler BA
    Ann Clin Lab Sci; 1981; 11(3):274-8. PubMed ID: 7018372
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Chemical pathology of amino acid diseases.
    Carson NA
    Acta Neurol Psychiatr Belg; 1968 Apr; 68(4):231-44. PubMed ID: 4972604
    [No Abstract]   [Full Text] [Related]  

  • 28. Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.
    Levy HL; Barkin E
    J Lab Clin Med; 1971 Oct; 78(4):517-23. PubMed ID: 5114049
    [No Abstract]   [Full Text] [Related]  

  • 29. [Inherited amino acid transport disorders].
    Igarashi Y; Tada K
    Nihon Rinsho; 1992 Jul; 50(7):1587-92. PubMed ID: 1404888
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Neuropathological study of aminoacidurias.
    Martin JJ; Schlote W
    Monogr Hum Genet; 1972; 6():64-78. PubMed ID: 4663916
    [No Abstract]   [Full Text] [Related]  

  • 31. Aminoacidurias due to inherited disorders of metabolism. 2.
    Frimpter GW
    N Engl J Med; 1973 Oct; 289(17):895-901. PubMed ID: 4598151
    [No Abstract]   [Full Text] [Related]  

  • 32. Phenylketonuria and other disorders of amino acid metabolism.
    Ampola MG
    Pediatr Clin North Am; 1973 May; 20(2):507-36. PubMed ID: 4573597
    [No Abstract]   [Full Text] [Related]  

  • 33. Ocular manifestations in aminoacidopathies.
    François J
    Adv Ophthalmol; 1972; 25():28-103. PubMed ID: 4560371
    [No Abstract]   [Full Text] [Related]  

  • 34. [5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report].
    Thalhammer O; Scheibenreiter S; Schön R; Knoll E; Schmierer G
    Wien Klin Wochenschr; 1972; 84():Suppl 2:3-12. PubMed ID: 5085466
    [No Abstract]   [Full Text] [Related]  

  • 35. Disorders of renal amino acid transport.
    Segal S
    N Engl J Med; 1976 May; 294(19):1044-51. PubMed ID: 943698
    [No Abstract]   [Full Text] [Related]  

  • 36. Inborn errors of amino acid metabolism and hereditary ataxia.
    Gaull GE
    Adv Neurol; 1978; 21():257-65. PubMed ID: 735926
    [No Abstract]   [Full Text] [Related]  

  • 37. Sulfur amino acids, hyperglycinemia, and certain possibly benign conditions.
    Frimpter GW
    Clin Perinatol; 1976 Mar; 3(1):53-9. PubMed ID: 954345
    [No Abstract]   [Full Text] [Related]  

  • 38. Absorption of amino acids and peptides in a child with a variant of Hartnup disease and coexistent coeliac disease.
    Tarlow MJ; Seakins JW; Lloyd JK; Matthews DM; Cheng B; Thomas AJ
    Arch Dis Child; 1972 Oct; 47(255):798-803. PubMed ID: 5086513
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Neonatal screening for inborn errors of amino acid metabolism.
    Levy HL
    Clin Endocrinol Metab; 1974 Mar; 3(1):153-66. PubMed ID: 4609646
    [No Abstract]   [Full Text] [Related]  

  • 40. [Amino acid metabolism pathology in the convulsive syndrome in young children].
    Alimov IIu; Iur'eva EA; Marchenko ZM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1972; 72(10):1497-500. PubMed ID: 4660427
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.