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Items: 1 to 20 of 103

1.

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.

2.

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. doi: 10.1007/s00431-012-1802-9. Epub 2012 Jul 29.

PMID:
22843301
3.

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. doi: 10.1111/j.1399-0004.2010.01440.x.

PMID:
20486940
4.

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.

PMID:
8844006
5.

Nephrolithiasis in a child with glucose-galactose malabsorption.

Tasic V, Slaveska N, Blau N, Santer R.

Pediatr Nephrol. 2004 Feb;19(2):244-6. Epub 2003 Dec 11.

PMID:
14673631
6.

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. No abstract available.

PMID:
15795603
7.

[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. doi: 10.1016/j.arcped.2012.09.005. Epub 2012 Oct 26. French.

PMID:
23107089
8.

[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. French.

PMID:
8319109
9.

Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1.

Soylu OB, Ecevit C, Altinöz S, Oztürk AA, Temizkan AK, Maeda M, Kasahara M.

Eur J Pediatr. 2008 Dec;167(12):1395-8. doi: 10.1007/s00431-008-0681-6. Epub 2008 Feb 21.

PMID:
18288487
10.

[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. Review. French.

PMID:
8250522
12.

Glucose-galactose malabsorption in an Oriental-Iraqui Jewish family.

Lebenthal E, Garti R, Mathoth Y, Cohen BE, Katzenelson D.

J Pediatr. 1971 May;78(5):844-50. No abstract available.

PMID:
5581590
13.

[Congential malabsorption of glucose and galactose in 2 brothers].

Kawakami E, Silvestrini WS, Machado NL, Wehba J, Fagundes Neto U.

Arq Gastroenterol. 1982 Jan-Mar;19(1):38-43. Portuguese.

PMID:
7181724
14.

Congenital glucose galactose malabsorption.

Wickramasinghe P, Lamabadusuriya SP, Lalani HA.

Ceylon Med J. 2001 Mar;46(1):26-7. No abstract available.

PMID:
11569998
15.

[Congenital malabsorption of glucose-galactose. Apropos of 2 cases].

Garcia P, Faverge B, Coignet J.

Ann Pediatr (Paris). 1987 Apr;34(4):317-20. French. No abstract available.

PMID:
3605977
16.

Molecular basis for glucose-galactose malabsorption.

Wright EM, Turk E, Martin MG.

Cell Biochem Biophys. 2002;36(2-3):115-21. Review.

PMID:
12139397
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.

PMID:
9404340
18.

Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects.

Lam JT, Martín MG, Turk E, Hirayama BA, Bosshard NU, Steinmann B, Wright EM.

Biochim Biophys Acta. 1999 Feb 24;1453(2):297-303.

19.

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 28;350(6316):354-6.

PMID:
2008213
20.

Absorption of glucose and maltose in congenital glucose-galactose malabsorption.

Fairclough PD, Clark ML, Dawson AM, Silk DB, Milla PJ, Harries JT.

Pediatr Res. 1978 Dec;12(12):1112-4.

PMID:
745864
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