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Best matches for Glucose-galactose malabsorption[title/abstract]:

SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption. Al-Suyufi Y et al. J Pediatr Gastroenterol Nutr. (2018)

Congenital glucose-galactose malabsorption diagnosed from macrohematuria in an infant. Yoshimura R et al. Pediatr Int. (2016)

Congenital Glucose-Galactose Malabsorption: A Case Report. Anderson S et al. J Pediatr Health Care. (2017)

Search results

Items: 1 to 20 of 129

1.

Congenital glucose-galactose malabsorption: A case report with a novel SLC5A1 mutation.

Al-Lawama M, Albaramki J, Altamimi M, El-Shanti H.

Clin Case Rep. 2018 Nov 11;7(1):51-53. doi: 10.1002/ccr3.1913. eCollection 2019 Jan.

2.

Congenital glucose-galactose malabsorption: A rare and severe cause of infant diarrhea.

Pascual Pérez AI, Martínez Velasco S, García Volpe C.

Med Clin (Barc). 2018 Nov 5. pii: S0025-7753(18)30562-1. doi: 10.1016/j.medcli.2018.09.002. [Epub ahead of print] English, Spanish. No abstract available.

PMID:
30409526
3.

Genetic Variants in SGLT1, Glucose Tolerance, and Cardiometabolic Risk.

Seidelmann SB, Feofanova E, Yu B, Franceschini N, Claggett B, Kuokkanen M, Puolijoki H, Ebeling T, Perola M, Salomaa V, Shah A, Coresh J, Selvin E, MacRae CA, Cheng S, Boerwinkle E, Solomon SD.

J Am Coll Cardiol. 2018 Oct 9;72(15):1763-1773. doi: 10.1016/j.jacc.2018.07.061.

4.

Development of SGLT1 and SGLT2 inhibitors.

Rieg T, Vallon V.

Diabetologia. 2018 Oct;61(10):2079-2086. doi: 10.1007/s00125-018-4654-7. Epub 2018 Aug 22. Review.

PMID:
30132033
5.

Altered pancreatic islet morphology and function in SGLT1 knockout mice on a glucose-deficient, fat-enriched diet.

Mühlemann M, Zdzieblo D, Friedrich A, Berger C, Otto C, Walles H, Koepsell H, Metzger M.

Mol Metab. 2018 Jul;13:67-76. doi: 10.1016/j.molmet.2018.05.011. Epub 2018 May 23.

6.

Novel and Unexpected Functions of SGLTs.

Wright EM, Ghezzi C, Loo DDF.

Physiology (Bethesda). 2017 Nov;32(6):435-443. doi: 10.1152/physiol.00021.2017. Review.

7.

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. doi: 10.1097/MPG.0000000000001694.

PMID:
28753187
8.

Causes Of Chronic Non-Infectious Diarrhoea In Infants Less Than 6 Months Of Age: Rarely Recognized Entities.

Mushtaq I, Cheema HA, Malik HS, Waheed N, Hashmi MA, Malik HS.

J Ayub Med Coll Abbottabad. 2017 Jan-Mar;29(1):78-82.

9.

Congenital Glucose-Galactose Malabsorption: A Case Report.

Anderson S, Koniaris S, Xin B, Brooks SS.

J Pediatr Health Care. 2017 Jul - Aug;31(4):506-510. doi: 10.1016/j.pedhc.2017.01.005. Epub 2017 Mar 7.

PMID:
28283348
10.

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. doi: 10.1159/000454951. Epub 2017 Feb 2.

PMID:
28152538
11.

Congenital glucose-galactose malabsorption diagnosed from macrohematuria in an infant.

Yoshimura R, Fujii T, Endo A, Kudo T, Shimizu T.

Pediatr Int. 2016 Dec;58(12):1365-1366. doi: 10.1111/ped.13047. No abstract available.

PMID:
28008736
12.

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. doi: 10.1007/s10620-016-4348-2. Epub 2016 Oct 25. No abstract available.

PMID:
27783308
13.

Diagnosing and Treating Intolerance to Carbohydrates in Children.

Berni Canani R, Pezzella V, Amoroso A, Cozzolino T, Di Scala C, Passariello A.

Nutrients. 2016 Mar 10;8(3):157. doi: 10.3390/nu8030157. Review.

14.

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 28;15:90. doi: 10.1186/s12876-015-0316-0.

15.

Congenital diseases of the gastrointestinal tract.

Lentze M.

Georgian Med News. 2014 May;(230):46-53. Review.

PMID:
24940857
16.

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. doi: 10.1016/j.ajg.2014.01.004. Epub 2014 Feb 1.

PMID:
24630509
17.

Glucose transport into everted sacs of the small intestine of mice.

Hamilton KL, Butt AG.

Adv Physiol Educ. 2013 Dec;37(4):415-26. doi: 10.1152/advan.00017.2013.

18.

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. doi: 10.1097/MPG.0000000000000114.

PMID:
24048166
19.

Five Arab children with glucose-galactose malabsorption.

Assiri A, Saeed A, Alnimri A, Ahmad S, Saeed E, Jameel S.

Paediatr Int Child Health. 2013 May;33(2):108-10. doi: 10.1179/2046905513Y.0000000055.

PMID:
23925285
20.

Glucose transport families SLC5 and SLC50.

Wright EM.

Mol Aspects Med. 2013 Apr-Jun;34(2-3):183-96. doi: 10.1016/j.mam.2012.11.002. Review.

PMID:
23506865

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