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PUBMED FOR HANDHELDS

Journal Abstract Search

150 related items for PubMed ID: 4365835

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Phenotypic expression of galactokinase deficiency in heterozygous and homozygous subjects: in vivo and in vitro studies.
    Benson PF, Brown SP, Cree J, Fensom AH, Grant AR.
    Birth Defects Orig Artic Ser; 1976; 12(3):305-12. PubMed ID: 182297
    [Abstract] [Full Text] [Related]

  • 23. [Quantitative enzymic determination of galactokinase activity in the erythrocyte haemolysate of patients with Down's syndrome (author's transl)].
    Lippross S, Menne F.
    Z Klin Chem Klin Biochem; 1974 Oct; 12(10):449-52. PubMed ID: 4279510
    [No Abstract] [Full Text] [Related]

  • 24. [Familial diphosphoglycerate mutase deficiency: hematological and biochemical study].
    Cartier P, Labie D, Leroux JP, Najman A, Demaugre F.
    Nouv Rev Fr Hematol; 1972 Oct; 12(3):269-87. PubMed ID: 4266202
    [No Abstract] [Full Text] [Related]

  • 25.
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  • 26. Induction of galactokinase in fibroblasts from heterozygous and homozygous subjects.
    Zacchello F, Benson PF, Brown S, Croll P, Giannelli F.
    Nat New Biol; 1972 Sep 20; 239(90):95-6. PubMed ID: 4512833
    [No Abstract] [Full Text] [Related]

  • 27.
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  • 28. [A new erythroenzymopathy: congenital non-spherocytic hemolytic anemia and hereditary erythrocytic adenylate kinase deficiency].
    Boivin P, Galand C, Hakim J, Simony D, Seligman M.
    Presse Med (1893); 1971 Jan 30; 79(6):215-8. PubMed ID: 5546784
    [No Abstract] [Full Text] [Related]

  • 29.
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  • 30. [Galactose loading test in infants and small children suffering in recurrent bronchitis and other chronic illness (author's transl)].
    Osváth P, Fornai K, Pozderka B, Veres B.
    Monatsschr Kinderheilkd; 1981 Aug 30; 129(8):460-3. PubMed ID: 6116185
    [Abstract] [Full Text] [Related]

  • 31.
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  • 32. Letter: Galactokinase deficiency in twins.
    Monteleone JA, Monteleone PL, Bert M, Hilliard R.
    Pediatrics; 1974 Nov 30; 54(5):656-8. PubMed ID: 4375802
    [No Abstract] [Full Text] [Related]

  • 33. Some inferences from galactokinase deficiency.
    Sidbury JB.
    Pediatrics; 1974 Mar 30; 53(3):309-10. PubMed ID: 4360929
    [No Abstract] [Full Text] [Related]

  • 34. Hereditary alpha1-antitrypsin deficiency and liver cirrhosis in children.
    Ostergaard PA.
    Dan Med Bull; 1973 Jun 30; 20(3):96-101. PubMed ID: 4543623
    [No Abstract] [Full Text] [Related]

  • 35. [Inborn errors of metabolism (author's transl)].
    Suzuki Y.
    No To Shinkei; 1978 Apr 30; 30(4):363-76. PubMed ID: 96846
    [No Abstract] [Full Text] [Related]

  • 36.
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  • 37. [Austrian programm for the early detection of inborn errors of metabolism].
    Thalhammer O, Scheibenreiter S, Biedl E.
    Wien Klin Wochenschr; 1970 Jan 02; 82(1):1-6. PubMed ID: 5513195
    [No Abstract] [Full Text] [Related]

  • 38.
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  • 39. [Alpha1-antitrypsin deficiency combined with hypoplasia of intrahepatic bile ducts (author's transl)].
    Haas H.
    Padiatr Padol; 1974 Jan 02; 9(3):261-5. PubMed ID: 4546986
    [No Abstract] [Full Text] [Related]

  • 40.
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