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Items: 1 to 20 of 102

1.

Interaction of Antipsychotic Drugs with Sucrase, Kinetics and Structural Study.

Jafari N, Dehganpour H, Ghavanini N, Mollasalehi H, Minai-Tehrani D.

Curr Clin Pharmacol. 2017;12(1):50-54. doi: 10.2174/1574884712666170118145901.

PMID:
28103775
2.

Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome.

Henström M, Diekmann L, Bonfiglio F, Hadizadeh F, Kuech EM, von Köckritz-Blickwede M, Thingholm LB, Zheng T, Assadi G, Dierks C, Heine M, Philipp U, Distl O, Money ME, Belheouane M, Heinsen FA, Rafter J, Nardone G, Cuomo R, Usai-Satta P, Galeazzi F, Neri M, Walter S, Simrén M, Karling P, Ohlsson B, Schmidt PT, Lindberg G, Dlugosz A, Agreus L, Andreasson A, Mayer E, Baines JF, Engstrand L, Portincasa P, Bellini M, Stanghellini V, Barbara G, Chang L, Camilleri M, Franke A, Naim HY, D'Amato M.

Gut. 2018 Feb;67(2):263-270. doi: 10.1136/gutjnl-2016-312456. Epub 2016 Nov 21.

3.

Congenital Sucrase-isomaltase Deficiency: A Novel Compound Heterozygous Mutation Causing Aberrant Protein Localization.

Haberman Y, Di Segni A, Loberman-Nachum N, Barel O, Kunik V, Eyal E, Kol N, Hout-Siloni G, Kochavi B, Avivi C, Schvimer M, Rechavi G, Anikster Y, Barshack I, Weiss B.

J Pediatr Gastroenterol Nutr. 2017 May;64(5):770-776. doi: 10.1097/MPG.0000000000001424.

PMID:
27749612
4.

Acetonic Extract from the Feijoa sellowiana Berg. Fruit Exerts Antioxidant Properties and Modulates Disaccharidases Activities in Human Intestinal Epithelial Cells.

Turco F, Palumbo I, Andreozzi P, Sarnelli G, De Ruberto F, Esposito G, Basile A, Cuomo R.

Phytother Res. 2016 Aug;30(8):1308-15. doi: 10.1002/ptr.5629. Epub 2016 May 10.

PMID:
27166598
5.

Diagnosing and Treating Intolerance to Carbohydrates in Children.

Berni Canani R, Pezzella V, Amoroso A, Cozzolino T, Di Scala C, Passariello A.

Nutrients. 2016 Mar 10;8(3):157. doi: 10.3390/nu8030157. Review.

6.

Congenital sucrase-isomaltase deficiency: diagnostic challenges and response to enzyme replacement therapy.

Puntis JW, Zamvar V.

Arch Dis Child. 2015 Sep;100(9):869-71. doi: 10.1136/archdischild-2015-308388. Epub 2015 Jul 10.

PMID:
26163121
7.

Old meets new: identifying founder mutations in genetic disease.

Evans JA.

CMAJ. 2015 Feb 3;187(2):93-4. doi: 10.1503/cmaj.141509. Epub 2015 Jan 19. No abstract available.

8.

Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.

Marcadier JL, Boland M, Scott CR, Issa K, Wu Z, McIntyre AD, Hegele RA, Geraghty MT, Lines MA.

CMAJ. 2015 Feb 3;187(2):102-7. doi: 10.1503/cmaj.140657. Epub 2014 Dec 1.

9.

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.

10.

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
11.

Inhibition of maltase-glucoamylase activity to hydrolyze α-1,4 linkages by the presence of undigested sucrose.

Lee BH, Quezada-Calvillo R, Nichols BL Jr, Rose DR, Hamaker BR.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S45-7. doi: 10.1097/01.mpg.0000421415.95751.f7. No abstract available.

PMID:
23103657
12.

Direct starch digestion by sucrase-isomaltase and maltase-glucoamylase.

Lin AH, Hamaker BR, Nichols BL Jr.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S43-5. doi: 10.1097/01.mpg.0000421414.95751.be. No abstract available.

PMID:
23103656
13.

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
14.

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.

15.

Four mutations in the SI gene are responsible for the majority of clinical symptoms of CSID.

Uhrich S, Wu Z, Huang JY, Scott CR.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S34-5. doi: 10.1097/01.mpg.0000421408.65257.b5. No abstract available.

PMID:
23103650
16.

Poor starch digestion in children with CSID and recurrent abdominal pain.

Robayo-Torres CC, Baker SS, Chumpitazi BP, Lecea CE, Nichols BL Jr, Opekun AR.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S32-4. doi: 10.1097/01.mpg.0000421407.88128.5c. No abstract available.

PMID:
23103649
17.

Phenotypic observations by the CSID Dietary and Medical Support Group.

Slawson MH.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S30-2. doi: 10.1097/01.mpg.0000421406.80504.1d. No abstract available.

PMID:
23103648
18.

Frequency of sucrase deficiency in mucosal biopsies.

Nichols BL Jr, Adams B, Roach CM, Ma CX, Baker SS.

J Pediatr Gastroenterol Nutr. 2012 Nov;55 Suppl 2:S28-30. doi: 10.1097/01.mpg.0000421405.42386.64. No abstract available.

PMID:
23103647
19.

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
20.

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

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