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 *

545 related articles for article (PubMed ID: 18428423)

  • 1. Diagnosis of inherited disorders of galactose metabolism.
    Cuthbert C; Klapper H; Elsas L
    Curr Protoc Hum Genet; 2008 Jan; Chapter 17():Unit 17.5. PubMed ID: 18428423
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare cases of galactose metabolic disorders: identification of more than two mutations per patient.
    Schulpis KH; Thodi G; Chatzidaki M; Iakovou K; Molou E; Dotsikas Y; Loukas YL
    J Pediatr Endocrinol Metab; 2017 Oct; 30(10):1119-1120. PubMed ID: 28902631
    [No Abstract]   [Full Text] [Related]  

  • 3. Molecular basis of disorders of human galactose metabolism: past, present, and future.
    Novelli G; Reichardt JK
    Mol Genet Metab; 2000; 71(1-2):62-5. PubMed ID: 11001796
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary galactosemia.
    Demirbas D; Coelho AI; Rubio-Gozalbo ME; Berry GT
    Metabolism; 2018 Jun; 83():188-196. PubMed ID: 29409891
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Galactosemia].
    Ohtake A; Amemiya S
    Nihon Rinsho; 2006 Sep; Suppl 3():215-9. PubMed ID: 17022534
    [No Abstract]   [Full Text] [Related]  

  • 6. Galactosemia: when is it a newborn screening emergency?
    Berry GT
    Mol Genet Metab; 2012 May; 106(1):7-11. PubMed ID: 22483615
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two familial cases of high blood galactose of unknown aetiology.
    Brunetti-Pierri N; Opekun AR; Craigen WJ
    J Inherit Metab Dis; 2006 Dec; 29(6):762. PubMed ID: 16988899
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Galactose and cataract.
    Stambolian D
    Surv Ophthalmol; 1988; 32(5):333-49. PubMed ID: 3043741
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The molecular basis of galactosemia - Past, present and future.
    Timson DJ
    Gene; 2016 Sep; 589(2):133-41. PubMed ID: 26143117
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Issues on universal screening for galactosemia.
    Padilla CD; Lam ST
    Ann Acad Med Singap; 2008 Dec; 37(12 Suppl):39-3. PubMed ID: 19904445
    [TBL] [Abstract][Full Text] [Related]  

  • 11. GALT Deficiency Galactosemia.
    Anderson S
    MCN Am J Matern Child Nurs; 2018; 43(1):44-51. PubMed ID: 29215423
    [TBL] [Abstract][Full Text] [Related]  

  • 12. On the screening for inborn errors of galactose metabolism.
    Vaca G; Sànchez-Corona J; Olivares N; Medina C; Ibarra B; Cantú JM
    Ann Genet; 1983; 26(3):191-2. PubMed ID: 6606384
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Perinatal galactose metabolism.
    Kliegman RM; Sparks JW
    J Pediatr; 1985 Dec; 107(6):831-41. PubMed ID: 3906069
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Galactose-1-phosphate uridyltransferase deficiency].
    Okano Y; Isshiki G
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):15-21. PubMed ID: 9589977
    [No Abstract]   [Full Text] [Related]  

  • 15. Structure and function of enzymes of the Leloir pathway for galactose metabolism.
    Holden HM; Rayment I; Thoden JB
    J Biol Chem; 2003 Nov; 278(45):43885-8. PubMed ID: 12923184
    [No Abstract]   [Full Text] [Related]  

  • 16. Human UDP-galactose 4' epimerase (GALE) gene and identification of five missense mutations in patients with epimerase-deficiency galactosemia.
    Maceratesi P; Daude N; Dallapiccola B; Novelli G; Allen R; Okano Y; Reichardt J
    Mol Genet Metab; 1998 Jan; 63(1):26-30. PubMed ID: 9538513
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intracellular galactose-1-phosphate accumulation leads to environmental stress response in yeast model.
    Slepak T; Tang M; Addo F; Lai K
    Mol Genet Metab; 2005 Nov; 86(3):360-71. PubMed ID: 16169270
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Galactose toxicity in animals.
    Lai K; Elsas LJ; Wierenga KJ
    IUBMB Life; 2009 Nov; 61(11):1063-74. PubMed ID: 19859980
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Identification of inborn errors of galactose metabolism in patients with cataracts].
    Vaca-Pacheco G; Medina C; García-Cruz D; Sánchez-Corona J; Chávez-Anaya E; Jaimes C; Hernández-Córdova A
    Arch Invest Med (Mex); 1990; 21(2):127-32. PubMed ID: 2103700
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ultra fast and sensitive liquid chromatography tandem mass spectrometry based assay for galactose-1-phosphate uridylyltransferase and galactokinase deficiencies.
    Li Y; Ptolemy AS; Harmonay L; Kellogg M; Berry GT
    Mol Genet Metab; 2011 Jan; 102(1):33-40. PubMed ID: 20863731
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 28.