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 *

242 related articles for article (PubMed ID: 5136311)

  • 21. Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
    World Health Organ Tech Rep Ser; 1968; 401():1-57. PubMed ID: 4973455
    [No Abstract]   [Full Text] [Related]  

  • 22. Pediatric clinical aspects of aminoacidopathies.
    Hooft C; Carton D
    Monogr Hum Genet; 1972; 6():50-63. PubMed ID: 4663915
    [No Abstract]   [Full Text] [Related]  

  • 23. [Disorders of amino acids].
    Aoki K
    Nihon Rinsho; 1993 Jan; 51 Suppl():332-9. PubMed ID: 8459561
    [No Abstract]   [Full Text] [Related]  

  • 24. [Methods and results of screening newborn infants for aminoacidopathies].
    Bickel H
    Monatsschr Kinderheilkd (1902); 1976 Sep; 129(9):650-3. PubMed ID: 979984
    [No Abstract]   [Full Text] [Related]  

  • 25. [Biochemical studies on inherited disorders of amino acid metabolism in pediatrics].
    Antener I
    Z Klin Chem Klin Biochem; 1970 Sep; 7(5):427-39. PubMed ID: 5505952
    [No Abstract]   [Full Text] [Related]  

  • 26. A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
    EFRON ML; YOUNG D; MOSER HW; MACCREADY RA
    N Engl J Med; 1964 Jun; 270():1378-83. PubMed ID: 14152868
    [No Abstract]   [Full Text] [Related]  

  • 27. [Screening for aminoacidopathies in newborns by means of an aminoacid analyzer. Reference values and statistical determinations (author's transl)].
    Antonozzi I; Del Castello PG; Morisi G; Ceccarelli P
    Ann Ist Super Sanita; 1978; 14(4):781-91. PubMed ID: 756692
    [TBL] [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. Disorders of amino acid metabolism--1971.
    Menkes JH
    Calif Med; 1971 Oct; 115(4):14-23. PubMed ID: 5110588
    [No Abstract]   [Full Text] [Related]  

  • 30. [Combined and isolated forms of metabolic errors detected in children].
    Tănase-Mogoş I; Ciortoloman H; Grigorescu G; Popescu M; Ankăr V
    Physiologie; 1980; 17(1):57-66. PubMed ID: 6767256
    [No Abstract]   [Full Text] [Related]  

  • 31. [Rapid separation of aromatic and ramified amino acids by chromatography on ion exchange columns. Application to the surveillance of leucinosis and hyperphenylalaninemia].
    Rey F; Sivy M; Rey J
    Rev Eur Etud Clin Biol; 1972 Feb; 17(2):221-3. PubMed ID: 5055018
    [No Abstract]   [Full Text] [Related]  

  • 32. [Combined forms of metabolic errors detected in newborn infants].
    Tănase-Mogoş I; Ciortoloman H; Grigorescu G; Popescu M; Ankăr V
    Physiologie; 1978; 15(4):239-43. PubMed ID: 106407
    [No Abstract]   [Full Text] [Related]  

  • 33. Diagnosis and treatment: some diseases, syndromes, and conditions associated with an unusual odor.
    Cone TE
    Pediatrics; 1968 May; 41(5):993-5. PubMed ID: 5654847
    [No Abstract]   [Full Text] [Related]  

  • 34. Diagnosis and mangement of inherited aminoacidopathies in the newborn and the unborn.
    Rosenberg LE
    Clin Endocrinol Metab; 1974 Mar; 3(1):145-52. PubMed ID: 4609645
    [No Abstract]   [Full Text] [Related]  

  • 35. [Progressive encephalopathy after a symptom-free period in the newborn infant, due to disorders of amino acid metabolism. Illustrated with case histories of patients with hyperglycinemia and maple syrup urine disease].
    Raven EJ
    Ned Tijdschr Geneeskd; 1969 Oct; 113(42):1850-3. PubMed ID: 5344645
    [No Abstract]   [Full Text] [Related]  

  • 36. [Primary and secondary hyperaminoaciduria in children (review of the literature)].
    Lebedev VP; Iur'eva EA; Mukhina IuG; Buravina TA; Koroleva IA
    Vopr Okhr Materin Det; 1970 Nov; 15(11):64-8. PubMed ID: 4928437
    [No Abstract]   [Full Text] [Related]  

  • 37. A survey of inborn errors of amino acid metabolism and transport in man.
    Wellner D; Meister A
    Annu Rev Biochem; 1981; 50():911-68. PubMed ID: 6791581
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. [Phaenotypic aspects of hereditary aminoacidopathies (author's transl)].
    Becker K
    Monatsschr Kinderheilkd; 1981 Oct; 129(10):556-63. PubMed ID: 6801479
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Branched-chain organic acidurias.
    Ogier de Baulny H; Saudubray JM
    Semin Neonatol; 2002 Feb; 7(1):65-74. PubMed ID: 12069539
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.