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 *

107 related articles for article (PubMed ID: 5010327)

  • 1. [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]  

  • 2. [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]  

  • 3. Inborn errors of metabolism associated with unusual odors.
    Carpenter DG; Carter CH
    J Fla Med Assoc; 1970 May; 57(5):31-3. PubMed ID: 5449191
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. [Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer].
    Boisse J; Moatti N
    Ann Biol Clin (Paris); 1973; 31(4):249-55. PubMed ID: 4579284
    [No Abstract]   [Full Text] [Related]  

  • 6. Methionine malabsorption syndrome.
    Hooft C; Timmermans J; Snoeck J; Antener I; Oyaert W; Van den Hende C
    Ann Paediatr; 1965; 205(1):73-104. PubMed ID: 5897673
    [No Abstract]   [Full Text] [Related]  

  • 7. [Renal clearance of amino acid in a hyperprolinemic child].
    Dodinval P; Willems C; Heusden AM; Hainaut H; Gottschalk C
    J Genet Hum; 1969 Oct; 17(3):297-315. PubMed ID: 5387412
    [No Abstract]   [Full Text] [Related]  

  • 8. [Inborn errors of amino acid metabolism].
    Endo F
    Nihon Rinsho; 2004 Nov; 62 Suppl 11():562-6. PubMed ID: 15628476
    [No Abstract]   [Full Text] [Related]  

  • 9. [Hereditary digestive enzyme defects].
    Rey J
    Med Chir Dig; 1972; 1(1):41-4 contd. PubMed ID: 5054004
    [No Abstract]   [Full Text] [Related]  

  • 10. [Free amino acids in plasma. Normal values in pediatrics].
    Cohen AL; Monesiglio JC
    Arch Argent Pediatr; 1971 Sep; 69(7):281-7. PubMed ID: 5113471
    [No Abstract]   [Full Text] [Related]  

  • 11. Clinical aspects of disorders of the urea cycle.
    Snyderman SE
    Pediatrics; 1981 Aug; 68(2):284-9, 295-7. PubMed ID: 7267239
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. [The detection of aminoacidopathies causing mental retardation].
    Thiriar M; Vis HL
    Acta Paediatr Belg; 1966; 20(5):333-70. PubMed ID: 5330633
    [No Abstract]   [Full Text] [Related]  

  • 14. Loading tests in normal, heterozygos and homozygos individuals with histidine and methionine respectively. 107 tests (author's transl).
    Hammuri M; Scheibenreiter S
    Klin Padiatr; 1974 Jul; 186(4):319-24. PubMed ID: 4472842
    [No Abstract]   [Full Text] [Related]  

  • 15. [Diseases caused by altered intermediate metabolism of amino acids].
    Bulgarelli R; Berio A
    Minerva Nipiol; 1969; 19(6):328-61 contd. PubMed ID: 4923874
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. [Familial essential hyperprolinemia].
    Hainaut H; Hariga J; Willems C; Heusden A; Chapelle P
    Presse Med (1893); 1971 Apr; 79(21):945-8. PubMed ID: 5580522
    [No Abstract]   [Full Text] [Related]  

  • 18. [Homocystinuria].
    Hooft C; Carton D
    Verh K Vlaam Acad Geneeskd Belg; 1967; 29(2):119-51. PubMed ID: 6078458
    [No Abstract]   [Full Text] [Related]  

  • 19. [Interference of DL-methionine, used as a supplement in some soya milks, in urinary screenings for aminoacidopathies].
    Zammarchi E
    Minerva Pediatr; 1977 Apr; 29(12):863-6. PubMed ID: 577591
    [No Abstract]   [Full Text] [Related]  

  • 20. [Methods of detection of amino acid metabolic anomalies. Technical aspects and personal results].
    Farriaux JP; Adam E; Dautrevaux M; Fontaine G
    Pediatrie; 1968 Jun; 23(4):479-81. PubMed ID: 5738526
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.