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 *

165 related articles for article (PubMed ID: 5059573)

  • 1. [Galactosemia, generally with a fulminating course. 10 cases found through an early detection program].
    Scheibenreiter S; Thalhammer O
    Wien Klin Wochenschr; 1972 Feb; 84(6):93-6. PubMed ID: 5059573
    [No Abstract]   [Full Text] [Related]  

  • 2. Galactokinase deficiency as a cause of cataracts.
    Beutler E; Matsumoto F; Kuhl W; Krill A; Levy N; Sparkes R; Degnan M
    N Engl J Med; 1973 Jun; 288(23):1203-6. PubMed ID: 4700553
    [No Abstract]   [Full Text] [Related]  

  • 3. [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]  

  • 4. [Hypergalactosemia in newborns as uncovered by the Austrian screening program in 12 years (author's transl)].
    Thalhammer O; Scheibenreiter S; Knoll E; Wehle E
    Klin Padiatr; 1980 Nov; 192(6):613-9. PubMed ID: 6452554
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Induction of galactose-1-phosphate uridylyltransferase in rat liver by galactose and experimental galactosemia].
    Salganik RI; Solov'eva NA
    Vopr Med Khim; 1972; 18(5):472-7. PubMed ID: 4117776
    [No Abstract]   [Full Text] [Related]  

  • 6. Letter: Negative urine sugars in galactosemia.
    Harris RC
    Pediatrics; 1974 May; 53(5):768. PubMed ID: 4826738
    [No Abstract]   [Full Text] [Related]  

  • 7. A patient with hereditary galactokinase deficiency.
    Dahlqvist A; Gamstorp I; Madsen H
    Acta Paediatr Scand; 1970 Nov; 59(6):669-75. PubMed ID: 5482251
    [No Abstract]   [Full Text] [Related]  

  • 8. The lens, cataracts, and galactosemia.
    Cogan DG
    N Engl J Med; 1973 Jun; 288(23):1239-40. PubMed ID: 4700558
    [No Abstract]   [Full Text] [Related]  

  • 9. [Our present knowledge of galactosemia].
    Sitzmann FC
    Med Klin; 1968 May; 63(20):781-4. PubMed ID: 5706572
    [No Abstract]   [Full Text] [Related]  

  • 10. [Galactosemia caused by galactosephosphate uridylyltransferase].
    Lachmajer-Lutosławska M; Hoppe A
    Pediatr Pol; 1978 Jan; 53(1):85-8. PubMed ID: 643406
    [No Abstract]   [Full Text] [Related]  

  • 11. [A case of galactosemia caused by galactokinase deficiency].
    Bolgiani MP; Gallenca M; Barocelli PC
    Pediatr Med Chir; 1984; 6(2):333-5. PubMed ID: 6531256
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Galactosemia urine--screening with test paper].
    Johansson S; Thalme B; Werner B
    Lakartidningen; 1970 Sep; 67(40):4502-4. PubMed ID: 5477770
    [No Abstract]   [Full Text] [Related]  

  • 13. [Studies on a family with galactosemia].
    von Berg W
    Dtsch Med Wochenschr; 1969 Jan; 94(2):61-5. PubMed ID: 5782691
    [No Abstract]   [Full Text] [Related]  

  • 14. [Gene frequency of hereditary galactosemia with reference to the Duarte variant].
    Kaloud H; Sitzmann FC
    Z Kinderheilkd; 1972; 113(3):205-14. PubMed ID: 4674437
    [No Abstract]   [Full Text] [Related]  

  • 15. Screening for galactosemia. Studies of the gene frequencies for galactosemia and the Duarte variant.
    Beutler E
    Isr J Med Sci; 1973; 9(9):1323-9. PubMed ID: 4149512
    [No Abstract]   [Full Text] [Related]  

  • 16. [On a case of congenital galactosemia].
    Di Marco A; Dinelli P; Polito P
    Clin Pediatr (Bologna); 1966 Jun; 48(6):248-61. PubMed ID: 6011307
    [No Abstract]   [Full Text] [Related]  

  • 17. Galactosemia in the newborn.
    Erickson GW; Staunton HA; Straup NF
    J Indiana State Med Assoc; 1966 Oct; 59(10):1180-3. PubMed ID: 5978359
    [No Abstract]   [Full Text] [Related]  

  • 18. [Preliminary results with the rapid fluorescence test (Weidemann) as mass screening procedure for galactosaemia in newborn infants (author transl)].
    Schön R
    Wien Klin Wochenschr; 1976 Apr; 88(8):274-7. PubMed ID: 983084
    [TBL] [Abstract][Full Text] [Related]  

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

  • 20. Screening for galactosemia and glucose-6-phosphate dehydrogenase deficiency in newborn infants.
    Nelson K; Hsia DY
    J Pediatr; 1967 Oct; 71(4):582-5. PubMed ID: 4382952
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.