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 *

106 related articles for article (PubMed ID: 5078372)

  • 21. [Congenital hyperbilirubinemia].
    Dauchy F
    Gaz Med Fr; 1965 May; 72(9):1975-82. PubMed ID: 5839759
    [No Abstract]   [Full Text] [Related]  

  • 22. [Enzymopathies in childhood].
    Swoboda W
    Wien Klin Wochenschr; 1971 Apr; 83(17):298-301. PubMed ID: 5576980
    [No Abstract]   [Full Text] [Related]  

  • 23. [Panel discussion. Congenital anomaly in glucose metabolism].
    Nihon Shonika Gakkai Zasshi; 1966 Oct; 70(10):963-6. PubMed ID: 6010385
    [No Abstract]   [Full Text] [Related]  

  • 24. [Advances and significance of genetics in pediatrics. Hereditary enzyme defects].
    Prader A
    Monatsschr Kinderheilkd (1902); 1966 Apr; 114(4):188-93. PubMed ID: 5985791
    [No Abstract]   [Full Text] [Related]  

  • 25. [Differential diagnosis between hereditary fructose intolerance and fructose-1,6-diphosphatase deficiency].
    Méndez Aparicio FM
    Rev Clin Esp; 1981 Jun 15-30; 161(5-6):289-96. PubMed ID: 6270745
    [No Abstract]   [Full Text] [Related]  

  • 26. [Pediatric liver diseases].
    Labrune P; Myara A; Imbert-Bismut F; Gerhardt MF
    Pathol Biol (Paris); 1999 Nov; 47(9):966-73. PubMed ID: 10609277
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Problems of phenotypic similarity and differential diagnostic of hereditary diseases in children].
    Barashnev IuI
    Vestn Akad Med Nauk SSSR; 1982; (6):47-51. PubMed ID: 7051616
    [No Abstract]   [Full Text] [Related]  

  • 28. [Studies on lipid metabolism in childhood. On the significance of lecithin: cholesterol fatty acyl transferase determination in various child liver diseases].
    Imamura S
    Sapporo Igaku Zasshi; 1968; 34(2):90-8. PubMed ID: 5753282
    [No Abstract]   [Full Text] [Related]  

  • 29. [Study of the alkaline phophatase and 5-nucleotidase activity of the serum. Clinical and experimental results].
    Housset E; Etienne JP ETITE JP
    Rev Int Hepatol; 1967 May; 17(6):519-36. PubMed ID: 5585947
    [No Abstract]   [Full Text] [Related]  

  • 30. [Hereditary intolerance to fructose].
    Mariani R; Siino A; Richert J; Bernard R
    Mars Med; 1969; 106(2):127-43. PubMed ID: 5768598
    [No Abstract]   [Full Text] [Related]  

  • 31. Therapy in congenital hyperbilirubinemia: phenobarbital and diethylnicotinamide.
    Ertel IJ; Newton WA
    Pediatrics; 1969 Jul; 44(1):43-8. PubMed ID: 5795402
    [No Abstract]   [Full Text] [Related]  

  • 32. [Intestinal disaccharidases enzyme activity. Its reduction in enteropathy caused by gluten and in other conditions of malabsorption].
    De Larrechea I; Sampayo RR; Sosa Miatello C; Ibarra R
    Prensa Med Argent; 1966 Jul; 53(26):1421-5. PubMed ID: 5999675
    [No Abstract]   [Full Text] [Related]  

  • 33. [Hereditary fructose intolerance].
    Vaisman N; Cooper M; Garti R
    Harefuah; 1981 May; 100(10):464-6. PubMed ID: 7308886
    [No Abstract]   [Full Text] [Related]  

  • 34. [Growth of patients with hereditary fructose intolerance or hereditary saccharose-isomaltose malabsorption].
    Nüssli R
    Helv Paediatr Acta; 1971 Dec; 26(5):637-47. PubMed ID: 5142943
    [No Abstract]   [Full Text] [Related]  

  • 35. [Congenital disorders of carbohydrate metabolism in children].
    Rosenkranz A
    Wien Med Wochenschr; 1965 Nov; 115(45):953-7. PubMed ID: 5221113
    [No Abstract]   [Full Text] [Related]  

  • 36. [Ocular complications of congenital metabolism errors].
    Goux JP; Kallay O
    Bull Soc Belge Ophtalmol; 1971; 157(1):9-322. PubMed ID: 5565533
    [No Abstract]   [Full Text] [Related]  

  • 37. [Determination of blood serum 5'-nucleotidase activity in differential diagnosis of jaundice].
    Braginskiĭ DM; Paktoris EA; Sinaĭko GA; Shakhgil'ian IV
    Sov Med; 1980; (6):49-52. PubMed ID: 6251570
    [No Abstract]   [Full Text] [Related]  

  • 38. 'In vitro' assay of bilirubin-UDP glucuronyl transferase activity in the liver of patients with Gilbert's syndrome and a variety of hepatic disorders.
    Black M; Billing BH
    Gut; 1968 Dec; 9(6):728-9. PubMed ID: 5717986
    [No Abstract]   [Full Text] [Related]  

  • 39. [Serum 5'nucleotidases: experimental and clinical study].
    Pappo E; Christoforov B; Petite JP; Boulu R; Etienne JP; Housset E
    Actual Hepatogastroenterol (Paris); 1969; 5(7):B289+. PubMed ID: 5378655
    [No Abstract]   [Full Text] [Related]  

  • 40. [Hereditary fructose intolerance. Early manifestation in newborns and young infants (author's transl)].
    Vieweg B; Posselt HG; Streb H; Strobel S
    Monatsschr Kinderheilkd; 1982 Jan; 130(1):21-6. PubMed ID: 7062914
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.