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 *

125 related articles for article (PubMed ID: 117252)

  • 41. Prenatal diagnosis of galactosaemia.
    Ng WG; Donnell GN; Alfi O
    Lancet; 1977 Jan; 1(8001):43-4. PubMed ID: 63680
    [No Abstract]   [Full Text] [Related]  

  • 42. Problems in the diagnosis of transferase and galactokinase deficient galactosemia.
    Pesce MA; Bodourian SH
    Ann Clin Lab Sci; 1980; 10(1):26-32. PubMed ID: 7362195
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Prenatal diagnosis of galactose-1-phosphate uridyltransferase (GALT)-deficient galactosemia.
    Elsas LJ
    Prenat Diagn; 2001 Apr; 21(4):302-3. PubMed ID: 11288121
    [No Abstract]   [Full Text] [Related]  

  • 44. Mutations at the galactose-1-p-uridyltransferase gene in infants with a positive galactosemia newborn screening test.
    Item C; Hagerty BP; Mühl A; Greber-Platzer S; Stöckler-Ipsiroglu S; Strobl W
    Pediatr Res; 2002 Apr; 51(4):511-6. PubMed ID: 11919338
    [TBL] [Abstract][Full Text] [Related]  

  • 45. THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES. A PRESUMED TEST FOR HETEROZYGOUS CARRIERS OF THE GALACTOSEMIC DEFECT.
    ROBINSON A
    J Exp Med; 1963 Sep; 118(3):359-70. PubMed ID: 14077997
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Simultaneous amplification, detection, and analysis of common mutations in the galactose-1-phosphate uridyl transferase gene.
    Jama M; Nelson L; Pont-Kingdon G; Mao R; Lyon E
    J Mol Diagn; 2007 Nov; 9(5):618-23. PubMed ID: 17884932
    [TBL] [Abstract][Full Text] [Related]  

  • 47. On the molecular nature of the Duarte variant of galactose-1-phosphate uridyl transferase (GALT).
    Lin HC; Kirby LT; Ng WG; Reichardt JK
    Hum Genet; 1994 Feb; 93(2):167-9. PubMed ID: 8112740
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Galactosaemia: relationship of IQ to biochemical control and genotype.
    Cleary MA; Heptinstall LE; Wraith JE; Walter JH
    J Inherit Metab Dis; 1995; 18(2):151-2. PubMed ID: 7564232
    [No Abstract]   [Full Text] [Related]  

  • 49. [Prenatal and postnatal determination of galactose-1-phosphate uridyltransferase genotypes].
    Christensen E; Brandt NJ
    Ugeskr Laeger; 1979 Nov; 141(47):3215-7. PubMed ID: 524501
    [No Abstract]   [Full Text] [Related]  

  • 50. [Galactosemia and cow's milk intolerance (author's transl)].
    Gómez de Terreros I; Gayoso Gómez F; Senín Sánchez J; Castro Gómez A; Muñóz Conde J; de la Rosa A
    An Esp Pediatr; 1978 Feb; 11(2):157-64. PubMed ID: 655510
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The use of glucose-1-[32P]phosphate for the determination of hexose-1-phosphate uridyl transferase activity in red blood cells.
    Grodzka Z; Chojnacki T
    Biochem Med; 1976 Dec; 16(3):182-6. PubMed ID: 1016259
    [No Abstract]   [Full Text] [Related]  

  • 52. Development of a protocol for newborn screening for disorders of the galactose metabolic pathway.
    Bowling FG; Brown AR
    J Inherit Metab Dis; 1986; 9(1):99-104. PubMed ID: 3014213
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Galactosaemia and the problem of galactose toxicity.
    Schwarz V
    Biochem Soc Trans; 1975; 3(2):234-8. PubMed ID: 165990
    [No Abstract]   [Full Text] [Related]  

  • 54. ERYTHROCYTIC GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE LEVELS IN HEPATIC CIRRHOSIS.
    FISHER MM; SPEAR S; SAMOLS E; SHERLOCK S
    Gut; 1964 Apr; 5(2):170-2. PubMed ID: 14159408
    [No Abstract]   [Full Text] [Related]  

  • 55. The molecular relationship between deficient UDP-galactose uridyl transferase (GALT) and ceramide galactosyltransferase (CGT) enzyme function: a possible cause for poor long-term prognosis in classic galactosemia.
    Lebea PJ; Pretorius PJ
    Med Hypotheses; 2005; 65(6):1051-7. PubMed ID: 16125333
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Transferase-deficiency galactosemia: immunochemical studies of the Duarte and Los Angeles variants.
    Andersen MW; Williams VP; Sparkes MC; Sparkes RS
    Hum Genet; 1984; 65(3):287-90. PubMed ID: 6321325
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Borderline galactosemia.
    Pettersson R; Dahlqvist A; Hattevig G; Kjellman B
    Acta Paediatr Scand; 1980 Nov; 69(6):735-9. PubMed ID: 7211358
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A yeast model reveals biochemical severity associated with each of three variant alleles of galactose-1P uridylyltransferase segregating in a single family.
    Chhay JS; Openo KK; Eaton JS; Gentile M; Fridovich-Keil JL
    J Inherit Metab Dis; 2008 Feb; 31(1):97-107. PubMed ID: 18210213
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [The frequency of uridyl transferase deficiency in patients with galactose intolerance].
    Fernekorn A; Fiehring C
    Dtsch Gesundheitsw; 1976 Dec; 31(52):2455-60. PubMed ID: 1009846
    [No Abstract]   [Full Text] [Related]  

  • 60. Biochemical characterization of the S135L allele of galactose-1-phosphate uridylyltransferase associated with galactosaemia.
    Wells L; Fridovich-Keil JL
    J Inherit Metab Dis; 1997 Sep; 20(5):633-42. PubMed ID: 9323558
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.