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Results: 1 to 20 of 99

1.

Congenital sucrase-isomaltase deficiency: an under-diagnosed disease in Chinese children.

Geng L, Li DY, Ou W, Yang Q, Fang T, Chen P, Yang M, Gong S.

BMC Pediatr. 2014 Jan 16;14:11. doi: 10.1186/1471-2431-14-11.

PMID:
24433566
[PubMed - in process]
Free PMC Article
2.

13C-breath tests for sucrose digestion in congenital sucrase isomaltase-deficient and sacrosidase-supplemented patients.

Robayo-Torres CC, Opekun AR, Quezada-Calvillo R, Villa X, Smith EO, Navarrete M, Baker SS, Nichols BL.

J Pediatr Gastroenterol Nutr. 2009 Apr;48(4):412-8.

PMID:
19330928
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Sacrosidase therapy for congenital sucrase-isomaltase deficiency.

Treem WR, McAdams L, Stanford L, Kastoff G, Justinich C, Hyams J.

J Pediatr Gastroenterol Nutr. 1999 Feb;28(2):137-42.

PMID:
9932843
[PubMed - indexed for MEDLINE]
4.

Diagnostic value of sucrose tolerance test in children evaluated by breath hydrogen measurement.

Douwes AC, Fernandes J, Jongbloed AA.

Acta Paediatr Scand. 1980 Jan;69(1):79-82.

PMID:
7368916
[PubMed - indexed for MEDLINE]
5.

Glucose polymer as a cause of protracted diarrhea in infants with unsuspected congenital sucrase-isomaltase deficiency.

Newton T, Murphy MS, Booth IW.

J Pediatr. 1996 Jun;128(6):753-6.

PMID:
8648532
[PubMed - indexed for MEDLINE]
6.

Evaluation of liquid yeast-derived sucrase enzyme replacement in patients with sucrase-isomaltase deficiency.

Treem WR, Ahsan N, Sullivan B, Rossi T, Holmes R, Fitzgerald J, Proujansky R, Hyams J.

Gastroenterology. 1993 Oct;105(4):1061-8.

PMID:
8405850
[PubMed - indexed for MEDLINE]
7.

Sucrase-isomaltase deficiency. A follow-up report.

Kilby A, Burgess EA, Wigglesworth S, Walker-Smith JA.

Arch Dis Child. 1978 Aug;53(8):677-9.

PMID:
708108
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency.

Harms HK, Bertele-Harms RM, Bruer-Kleis D.

N Engl J Med. 1987 May 21;316(21):1306-9.

PMID:
3553946
[PubMed - indexed for MEDLINE]
9.

Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption.

Sander P, Alfalah M, Keiser M, Korponay-Szabo I, Kovács JB, Leeb T, Naim HY.

Hum Mutat. 2006 Jan;27(1):119.

PMID:
16329100
[PubMed - indexed for MEDLINE]
10.

Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.

Belmont JW, Reid B, Taylor W, Baker SS, Moore WH, Morriss MC, Podrebarac SM, Glass N, Schwartz ID.

BMC Pediatr. 2002 Apr 25;2:4.

PMID:
12014995
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Outbreak of life-threatening thiamine deficiency in infants in Israel caused by a defective soy-based formula.

Fattal-Valevski A, Kesler A, Sela BA, Nitzan-Kaluski D, Rotstein M, Mesterman R, Toledano-Alhadef H, Stolovitch C, Hoffmann C, Globus O, Eshel G.

Pediatrics. 2005 Feb;115(2):e233-8.

PMID:
15687431
[PubMed - indexed for MEDLINE]
12.

[Clinical studies of pediatric malabsorption syndromes].

Hosoyamada T.

Fukuoka Igaku Zasshi. 2006 Nov;97(11):322-50. Japanese.

PMID:
17228786
[PubMed - indexed for MEDLINE]
13.

Clinical utility of serologic testing for celiac disease in ontario: an evidence-based analysis.

Health Quality Ontario.

Ont Health Technol Assess Ser. 2010;10(21):1-111. Epub 2010 Dec 1.

PMID:
23074399
[PubMed]
Free PMC Article
14.

Relative nephroprotection during Escherichia coli O157:H7 infections: association with intravenous volume expansion.

Ake JA, Jelacic S, Ciol MA, Watkins SL, Murray KF, Christie DL, Klein EJ, Tarr PI.

Pediatrics. 2005 Jun;115(6):e673-80.

PMID:
15930195
[PubMed - indexed for MEDLINE]
15.

Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.

Jacob R, Zimmer KP, Schmitz J, Naim HY.

J Clin Invest. 2000 Jul;106(2):281-7.

PMID:
10903344
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum.

Ritz V, Alfalah M, Zimmer KP, Schmitz J, Jacob R, Naim HY.

Gastroenterology. 2003 Dec;125(6):1678-85.

PMID:
14724820
[PubMed - indexed for MEDLINE]
17.

Detection of primary and secondary sucrose malabsorption in children by means of the breath hydrogen technique.

Davidson GP, Robb TA.

Med J Aust. 1983 Jul 9;2(1):29-32.

PMID:
6865823
[PubMed - indexed for MEDLINE]
18.

Breath hydrogen test and sucrase isomaltase deficiency.

Ford RP, Barnes GL.

Arch Dis Child. 1983 Aug;58(8):595-7.

PMID:
6614973
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Effect of feeding yogurt versus milk in children with acute diarrhea and carbohydrate malabsorption.

Boudraa G, Benbouabdellah M, Hachelaf W, Boisset M, Desjeux JF, Touhami M.

J Pediatr Gastroenterol Nutr. 2001 Sep;33(3):307-13.

PMID:
11593127
[PubMed - indexed for MEDLINE]
20.

Randomized, double-blind clinical trial of a lactose-free and a lactose-containing formula in dietary management of acute childhood diarrhea.

Simakachorn N, Tongpenyai Y, Tongtan O, Varavithya W.

J Med Assoc Thai. 2004 Jun;87(6):641-9.

PMID:
15279342
[PubMed - indexed for MEDLINE]

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