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2. 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]
3. Prenatal identification of a heterozygous status in two fetuses at risk for glucose-galactose malabsorption. Martín MG; Turk E; Kerner C; Zabel B; Wirth S; Wright EM Prenat Diagn; 1996 May; 16(5):458-62. PubMed ID: 8844006 [TBL] [Abstract][Full Text] [Related]
4. [Neonatal diarrhea due to congenital glucose-galactose malabsorption: report of seven cases]. Chedane-Girault C; Dabadie A; Maurage C; Piloquet H; Chailloux E; Colin E; Pelatan C; Giniès JL Arch Pediatr; 2012 Dec; 19(12):1289-92. PubMed ID: 23107089 [TBL] [Abstract][Full Text] [Related]
5. [Thirty years of research on congenital glucose and galactose malabsorption: from phenotype to genotype]. Desjeux JF; Wright EM Bull Acad Natl Med; 1993 Jan; 177(1):125-31; discussion 132-5. PubMed ID: 8319109 [TBL] [Abstract][Full Text] [Related]
6. [30 years' work on congenital glucose and galactose malabsorption: from phenotype to genotype]. Desjeux JF; Wright EM Ann Gastroenterol Hepatol (Paris); 1993 Oct; 29(5):263-6; discussion 266-8. PubMed ID: 8250522 [TBL] [Abstract][Full Text] [Related]
7. [Congential malabsorption of glucose and galactose in 2 brothers]. Kawakami E; Silvestrini WS; Machado NL; Wehba J; Fagundes Neto U Arq Gastroenterol; 1982; 19(1):38-43. PubMed ID: 7181724 [TBL] [Abstract][Full Text] [Related]
8. [Congenital malabsorption of glucose-galactose. Apropos of 2 cases]. Garcia P; Faverge B; Coignet J Ann Pediatr (Paris); 1987 Apr; 34(4):317-20. PubMed ID: 3605977 [No Abstract] [Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter. Turk E; Zabel B; Mundlos S; Dyer J; Wright EM Nature; 1991 Mar; 350(6316):354-6. PubMed ID: 2008213 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Nephrolithiasis in a child with glucose-galactose malabsorption. Tasic V; Slaveska N; Blau N; Santer R Pediatr Nephrol; 2004 Feb; 19(2):244-6. PubMed ID: 14673631 [TBL] [Abstract][Full Text] [Related]
16. Renal and intestinal hexose transport in familial glucose-galactose malabsorption. Elsas LJ; Hillman RE; Patterson JH; Rosenberg LE J Clin Invest; 1970 Mar; 49(3):576-85. PubMed ID: 5415683 [TBL] [Abstract][Full Text] [Related]
18. [Glucose-galactose malabsorption. The first reported case in Denmark]. Boisen KA; Hjelt K Ugeskr Laeger; 1999 Jun; 161(26):4008-9. PubMed ID: 10402938 [TBL] [Abstract][Full Text] [Related]
19. [Life-threatening diarrhea in the neonatal period. A case of congenital glucose-galactose malabsorption]. Bangstad HJ Tidsskr Nor Laegeforen; 1982 Nov; 102(33):1757-8. PubMed ID: 7167947 [No Abstract] [Full Text] [Related]