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Results: 12

1.

Clinical aspects and treatment of congenital sucrase-isomaltase deficiency.

Treem WR.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S7-13. doi: 10.1097/01.mpg.0000421401.57633.90. No abstract available.

PMID:
23103658
[PubMed - indexed for MEDLINE]
2.

Congenital sucrase-isomaltase deficiency: diet assessment and education guidelines.

McMeans AR.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S37-9. doi: 10.1097/01.mpg.0000421410.72880.ae. No abstract available.

PMID:
23103652
[PubMed - indexed for MEDLINE]
3.

Congenital sucrase-isomaltase deficiency: summary of an evaluation in one family.

Chumpitazi BP, Robayo-Torres CC, Opekun AR, Nichols BL Jr, Naim HY.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S36. doi: 10.1097/01.mpg.0000421409.65257.fc. No abstract available.

PMID:
23103651
[PubMed - indexed for MEDLINE]
4.

Starch digestion and patients with congenital sucrase-isomaltase deficiency.

Hamaker BR, Lee BH, Quezada-Calvillo R.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S24-8. doi: 10.1097/01.mpg.0000421404.42386.2d. No abstract available.

PMID:
23103646
[PubMed - indexed for MEDLINE]
5.

50 years of progress since congenital sucrase-isomaltase deficiency recognition.

Nichols BL Jr, Auricchio S.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S2-7. doi: 10.1097/01.mpg.0000421400.50010.2a. No abstract available.

PMID:
23103644
[PubMed - indexed for MEDLINE]
6.

Congenital sucrase-isomaltase deficiency: heterogeneity of inheritance, trafficking, and function of an intestinal enzyme complex.

Naim HY, Heine M, Zimmer KP.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S13-20. doi: 10.1097/01.mpg.0000421402.57633.4b. No abstract available.

PMID:
23103643
[PubMed - indexed for MEDLINE]
7.

Research progress reported at the 50th Anniversary of the Discovery of Congenital Sucrase-Isomaltase Deficiency Workshop.

Gilger M, Hamaker B, Nichols BL Jr, Auricchio S, Treem WR, Naim HY, Heine M, Zimmer KP, Jones K, Eskandari R, Pinto BM, Rose DR, Lee BH, Quezada-Calvillo R, Adams B, Roach CM, Ma CX, Baker SS, Slawson MH, Robayo-Torres CC, Chumpitazi BP, Lecea CE, Opekun AR, Uhrich S, Wu Z, Huang JY, Scott CR, Chumpitazi BP, McMeans AR, Scholz D, Shulman RJ, Ao Z, Sterchi EE, Lin AH.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S1. doi: 10.1097/01.mpg.0000422151.38401.69. No abstract available.

PMID:
23103641
[PubMed - indexed for MEDLINE]
8.

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
9.

Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency.

Alfalah M, Keiser M, Leeb T, Zimmer KP, Naim HY.

Gastroenterology. 2009 Mar;136(3):883-92. doi: 10.1053/j.gastro.2008.11.038. Epub 2008 Nov 19.

PMID:
19121318
[PubMed - indexed for MEDLINE]
10.

Altered folding, turnover, and polarized sorting act in concert to define a novel pathomechanism of congenital sucrase-isomaltase deficiency.

Keiser M, Alfalah M, Pröpsting MJ, Castelletti D, Naim HY.

J Biol Chem. 2006 May 19;281(20):14393-9. Epub 2006 Mar 16.

PMID:
16543230
[PubMed - indexed for MEDLINE]
Free Article
11.

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]
12.

A phenylalanine-based folding determinant in intestinal sucrase-isomaltase that functions in the context of a quality control mechanism beyond the endoplasmic reticulum.

Pröpsting MJ, Kanapin H, Jacob R, Naim HY.

J Cell Sci. 2005 Jun 15;118(Pt 12):2775-84.

PMID:
15944403
[PubMed - indexed for MEDLINE]
Free Article

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