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Items: 1 to 20 of 349

1.

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
3.

Molecular basis for glucose-galactose malabsorption.

Wright EM, Turk E, Martin MG.

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

PMID:
12139397
4.

[Selective congenital glucose, galactose malabsorption in the small intestine].

Bamba T, Fukuda M.

Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):552-4. Review. Japanese. No abstract available.

PMID:
9645131
5.

I. Glucose galactose malabsorption.

Wright EM.

Am J Physiol. 1998 Nov;275(5 Pt 1):G879-82. Review.

6.

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
7.

Malabsorption: molecular biology to the bedside.

Ghishan FK.

Gastroenterology. 1992 Sep;103(3):1105-6. No abstract available.

PMID:
1499914
8.

Glucose-galactose malabsorption.

[No authors listed]

N Engl J Med. 1966 Feb 10;274(6):351. No abstract available.

PMID:
5951901
9.

[Congenital malabsorption of glucose-galactose. A further case with study in vitro of intestinal absorption and study of TmG].

Beauvais P, Vaudour G, Desjeux JF, Le Balle JC, Girot JY, Brissaud HE.

Arch Fr Pediatr. 1971 Jun-Jul;28(6):573-91. French. No abstract available.

PMID:
5114943
10.

Structure of the human Na+/glucose cotransporter gene SGLT1.

Turk E, Martín MG, Wright EM.

J Biol Chem. 1994 May 27;269(21):15204-9.

11.

Congenital glucose galactose malabsorption.

Wickramasinghe P, Lamabadusuriya SP, Lalani HA.

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

PMID:
11569998
12.

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
13.

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
14.

Disorders of carbohydrate absorption.

Harries JT.

Clin Gastroenterol. 1982 Jan;11(1):17-36. Review. No abstract available.

PMID:
7037237
15.

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
16.

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.

17.

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.

PMID:
2638717
18.
19.

Glucose-galactose malabsorption. Report of a case with autoradiographic studies of a mucosal biopsy.

Schneider AJ, Kinter WB, Stirling CE.

N Engl J Med. 1966 Feb 10;274(6):305-12. No abstract available.

PMID:
5903212
20.

[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

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