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 *

175 related articles for article (PubMed ID: 26215149)

  • 1. A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe.
    Fazeli W; Kaczmarek S; Kirschstein M; Santer R
    BMC Gastroenterol; 2015 Jul; 15():90. PubMed ID: 26215149
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives.
    Wanes D; Husein DM; Naim HY
    Nutrients; 2019 Feb; 11(2):. PubMed ID: 30813293
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two novel mutations in the lactase gene in a Japanese infant with congenital lactase deficiency.
    Uchida N; Sakamoto O; Irie M; Abukawa D; Takeyama J; Kure S; Tsuchiya S
    Tohoku J Exp Med; 2012 May; 227(1):69-72. PubMed ID: 22688420
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital lactose intolerance is triggered by severe mutations on both alleles of the lactase gene.
    Diekmann L; Pfeiffer K; Naim HY
    BMC Gastroenterol; 2015 Mar; 15():36. PubMed ID: 25881162
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD).
    Torniainen S; Freddara R; Routi T; Gijsbers C; Catassi C; Höglund P; Savilahti E; Järvelä I
    BMC Gastroenterol; 2009 Jan; 9():8. PubMed ID: 19161632
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in the translated region of the lactase gene (LCT) underlie congenital lactase deficiency.
    Kuokkanen M; Kokkonen J; Enattah NS; Ylisaukko-Oja T; Komu H; Varilo T; Peltonen L; Savilahti E; Jarvela I
    Am J Hum Genet; 2006 Feb; 78(2):339-44. PubMed ID: 16400612
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Congenital lactase deficiency: Identification of a new mutation].
    Sala Coromina J; Vinaixa Vergés A; Garcia Puig R
    An Pediatr (Barc); 2015 May; 82(5):365-6. PubMed ID: 25468453
    [No Abstract]   [Full Text] [Related]  

  • 8. Congenital glucose-galactose malabsorption: a descriptive study of clinical characteristics and outcome from Western Saudi Arabia.
    Saadah OI; Alghamdi SA; Sindi HH; Alhunaitti H; Bin-Taleb YY; Alhussaini BH
    Arab J Gastroenterol; 2014 Mar; 15(1):21-3. PubMed ID: 24630509
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypomorphic variants of lactase-phlorizin hydrolase in congenital lactase deficiency are trafficking incompetent and functionally inactive.
    Marten LM; Wanes D; Stellbrinck T; Santer R; Naim HY
    Biochim Biophys Acta Mol Basis Dis; 2022 Apr; 1868(4):166338. PubMed ID: 35007711
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene.
    Atay FY; Derme T; Uras N; Ceylaner G; Ceylaner S; Sari FN; Oguz SS
    Dig Dis Sci; 2017 Jan; 62(1):280-281. PubMed ID: 27783308
    [No Abstract]   [Full Text] [Related]  

  • 11. [Congenital lactase deficiency--a more common disease than previously thought?].
    Torniainen S; Savilahti E; Järvelä I
    Duodecim; 2009; 125(7):766-70. PubMed ID: 19432082
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Rare Cause of Intractable Diarrhea of Infancy.
    Ali S; Tariq A; Ghuncha M
    J Coll Physicians Surg Pak; 2019 Jun; 29(6):S48-S49. PubMed ID: 31142420
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Literature review on congenital glucose-galactose malabsorption from 2001 to 2019.
    Wang W; Wang L; Ma M
    J Paediatr Child Health; 2020 Nov; 56(11):1779-1784. PubMed ID: 32946683
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two Cases of Mistaken Polyuria and Nephrocalcinosis in Infants with Glucose-Galactose Malabsorption: A Possible Role of 1,25(OH)2D3
.
    Fiscaletti M; Lebel MJ; Alos N; Benoit G; Jantchou P
    Horm Res Paediatr; 2017; 87(4):277-282. PubMed ID: 28152538
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Excellent agreement between genetic and hydrogen breath tests for lactase deficiency and the role of extended symptom assessment.
    Pohl D; Savarino E; Hersberger M; Behlis Z; Stutz B; Goetze O; Eckardstein AV; Fried M; Tutuian R
    Br J Nutr; 2010 Sep; 104(6):900-7. PubMed ID: 20398434
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
    Belmont JW; Reid B; Taylor W; Baker SS; Moore WH; Morriss MC; Podrebarac SM; Glass N; Schwartz ID
    BMC Pediatr; 2002 Apr; 2():4. PubMed ID: 12014995
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Nutrition management of congenital glucose-galactose malabsorption: a case study.
    Abad-Sinden A; Borowitz S; Meyers R; Sutphen J
    J Am Diet Assoc; 1997 Dec; 97(12):1417-21. PubMed ID: 9404340
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital Glucose-Galactose Malabsorption: A Case Report.
    Anderson S; Koniaris S; Xin B; Brooks SS
    J Pediatr Health Care; 2017; 31(4):506-510. PubMed ID: 28283348
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Impaired trafficking and subcellular localization of a mutant lactase associated with congenital lactase deficiency.
    Behrendt M; Keiser M; Hoch M; Naim HY
    Gastroenterology; 2009 Jun; 136(7):2295-303. PubMed ID: 19208354
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case of neonatal diarrhoea caused by congenital glucose-galactose malabsorption.
    Lee WS; Tay CG; Nazrul N; Paed M; Chai PF
    Med J Malaysia; 2009 Mar; 64(1):83-5. PubMed ID: 19852331
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.