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 *

171 related articles for article (PubMed ID: 27783308)

  • 1. 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]  

  • 2. SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption.
    Al-Suyufi Y; ALSaleem K; Al-Mehaidib A; Banemai M; Aldekhail WM; Al-Muhandes A; Mohammed M; Allam R; Jambi A; Ramzan K; Imtiaz F
    J Pediatr Gastroenterol Nutr; 2018 Feb; 66(2):250-252. PubMed ID: 28753187
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption.
    Gok F; Aydin HI; Kurt I; Gokcay E; Maeda M; Kasahara M
    J Pediatr Gastroenterol Nutr; 2005 Apr; 40(4):508-11. PubMed ID: 15795603
    [No Abstract]   [Full Text] [Related]  

  • 4. Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene.
    Vallaeys L; Van Biervliet S; De Bruyn G; Loeys B; Moring AS; Van Deynse E; Cornette L
    Eur J Pediatr; 2013 Mar; 172(3):409-11. PubMed ID: 22843301
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Nutrition management of congenital glucose-galactose malabsorption: Case report of a Chinese infant.
    Ma M; Long Q; Chen F; Zhang T; Lu M; Wang W; Chen L
    Medicine (Baltimore); 2019 Aug; 98(33):e16828. PubMed ID: 31415402
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital glucose-galactose malabsorption: A rare and severe cause of infant diarrhea.
    Pascual Pérez AI; Martínez Velasco S; García Volpe C
    Med Clin (Barc); 2019 May; 152(10):e55-e56. PubMed ID: 30409526
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. Long-Term Dietary Changes in Subjects with Glucose Galactose Malabsorption Secondary to Biallelic Mutations of SLC5A1.
    Chan AP; Namjoshi SS; Jardack PM; Maloney L; Ardjmand A; Jackson NN; Martin MG
    Dig Dis Sci; 2021 Dec; 66(12):4414-4422. PubMed ID: 33433815
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Selective congenital glucose, galactose malabsorption in the small intestine].
    Bamba T; Fukuda M
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):552-4. PubMed ID: 9645131
    [No Abstract]   [Full Text] [Related]  

  • 11. Molecular basis for glucose-galactose malabsorption.
    Wright EM; Turk E; Martin MG
    Cell Biochem Biophys; 2002; 36(2-3):115-21. PubMed ID: 12139397
    [TBL] [Abstract][Full Text] [Related]  

  • 12. D28G mutation in congenital glucose-galactose malabsorption.
    Kianifar HR; Talebi S; Talebi S; Tavakkol-Afshari J; Esmaili M; Davachi B; Brook A
    Arch Iran Med; 2007 Oct; 10(4):514-8. PubMed ID: 17903058
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14.
    Hoşnut FÖ; Janecke AR; Şahin G; Vogel GF; Lafcı NG; Bichler P; Müller T; Huber LA; Valovka T; Aksu AÜ
    Genes (Basel); 2023 Jun; 14(7):. PubMed ID: 37510265
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Glucose-galactose malabsorption--a report in a Chinese family.
    Quak SH; Chong AS; Low PS
    J Singapore Paediatr Soc; 1989; 31(3-4):126-8. PubMed ID: 2638717
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish.
    Xin B; Wang H
    Clin Genet; 2011 Jan; 79(1):86-91. PubMed ID: 20486940
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hypernatremic dehydration as a sign leading to the diagnosis of glucose-galactose malabsorption in breast-fed neonates.
    Steinherz R; Nitzan M; Iancu TC
    Helv Paediatr Acta; 1984 Aug; 39(3):275-7. PubMed ID: 6544312
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A missense mutation in the Na(+)/glucose cotransporter gene SGLT1 in a patient with congenital glucose-galactose malabsorption: normal trafficking but inactivation of the mutant protein.
    Kasahara M; Maeda M; Hayashi S; Mori Y; Abe T
    Biochim Biophys Acta; 2001 May; 1536(2-3):141-7. PubMed ID: 11406349
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Bitterness of glucose/galactose: novel mutations in the SLC5A1 gene.
    Pode-Shakked B; Reish O; Aktuglu-Zeybek C; Kesselman D; Dekel B; Bujanover Y; Anikster Y
    J Pediatr Gastroenterol Nutr; 2014 Jan; 58(1):57-60. PubMed ID: 24048166
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diagnostic problems in glucose-galactose malabsorption. A case report.
    Kaijser K; Ockerman PA
    Acta Paediatr Scand; 1970 Mar; 59(2):214-6. PubMed ID: 5442433
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.