Sucrose intolerance (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sucrose intolerance" in English language version.

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jalm.aaccjnls.org

Hackenmueller SA, Grenache DG (2016). "Reference intervals for intestinal disaccharidase activities determined from a non-reference population" (PDF). The Journal of Applied Laboratory Medicine. 1 (2): 172–80. doi:10.1373/jalm.2016.020388. PMID 33626784.

broadinstitute.org

gnomad.broadinstitute.org

"SI sucrase-isomaltase". gnomAD. Broad Institute.

cghjournal.org

Robayo-Torres CC, Quezada-Calvillo R, Nichols BL (2006). "Disaccharide digestion: clinical and molecular aspects". Clin Gastroenterol Hepatol. 4 (3): 276–87. doi:10.1016/j.cgh.2005.12.023. PMID 16527688.

doi.org

Baudon JJ, Veinberg F, Thioulouse E, Morgant G, Aymard P, Charritat JL (April 1996). "Sucrase-isomaltase deficiency: changing pattern over two decades". J. Pediatr. Gastroenterol. Nutr. 22 (3): 284–8. doi:10.1097/00005176-199604000-00010. PMID 8708882.
Sander P, Alfalah M, Keiser M, et al. (January 2006). "Novel mutations in the human sucrase-isomaltase (SI) gene that cause congenital carbohydrate malabsorption". Hum. Mutat. 27 (1): 119. doi:10.1002/humu.9392. PMID 16329100.
Uhrich, Stefanie; Wu, Zaining; Huang, Jie-Yu; Scott, C. Ronald (2012). "Four Mutations in the SI Gene Are Responsible for the Majority of Clinical Symptoms of CSID". Journal of Pediatric Gastroenterology and Nutrition. 55: S34–5. doi:10.1097/01.mpg.0000421408.65257.b5. PMID 23103650. S2CID 747500.
Treem, William R. (1995). "Congenital sucrase-isomaltase deficiency". J Pediatr Gastroenterol Nutrition. 21 (21): 1–14. doi:10.1097/00005176-199507000-00001. PMID 8576798.
Gericke B, Amir M, Naim HY (2016). "The multiple roles of sucrase-isomaltase in the intestinal physiology". Mol Cell Pediatr. 3 (1): 2–6. doi:10.1186/s40348-016-0033-y. PMC 4728165. PMID 26812950.
Cohen, SA (2016). "The clinical consequences of sucrase-isomaltase deficiency". Mol Cell Pediatr. 3 (1): 5. doi:10.1186/s40348-015-0028-0. PMC 4746203. PMID 26857124.
Treem, WR (2012). "Clinical aspects and treatment of congenital sucrase-isomaltase deficiency" (PDF). Pediatr Gastroenterol Nutr. 55 (suppl 2): S7-13. doi:10.1097/01.mpg.0000421401.57633.90. PMID 23103658. S2CID 7179223. Archived from the original (PDF) on 2019-03-03.
Hackenmueller SA, Grenache DG (2016). "Reference intervals for intestinal disaccharidase activities determined from a non-reference population" (PDF). The Journal of Applied Laboratory Medicine. 1 (2): 172–80. doi:10.1373/jalm.2016.020388. PMID 33626784.
Puertolas MV, Fifi AC (2018). "The role of disaccharidase deficiencies in functional abdominal pain disorders—a narrative review". Nutrients. 10 (12): E1835. doi:10.3390/nu10121835. PMC 6315563. PMID 30501067.
Robayo-Torres CC, Quezada-Calvillo R, Nichols BL (2006). "Disaccharide digestion: clinical and molecular aspects". Clin Gastroenterol Hepatol. 4 (3): 276–87. doi:10.1016/j.cgh.2005.12.023. PMID 16527688.
Alfalah M, Keiser M, Leeb T, Zimmer KP, Naim HY (2009). "Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency". Gastroenterology. 136 (3): 883–92. doi:10.1053/j.gastro.2008.11.038. PMID 19121318.
Jacob R, Zimmer KP, Schmitz J, Naim HY (2000). "Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme". J Clin Invest. 106 (2): 281–7. doi:10.1172/JCI9677. PMC 314311. PMID 10903344.
Keiser M, Alfalah M, Pröpsting MJ, Castelletti D, Naim HY (2006). "Altered folding, turnover, and polarized sorting act in concert to define a novel pathomechanism of congenital sucrase-isomaltase deficiency" (PDF). J Biol Chem. 281 (20): 14393–9. doi:10.1074/jbc.M513631200. PMID 16543230.
Naim HY, Heine M, Zimmer KP (2012). "Congenital sucrase-isomaltase deficiency: heterogeneity of inheritance, trafficking, and function of an intestinal enzyme complex". J Pediatr Gastroenterol Nutr. 55 (suppl 2): S13-20. doi:10.1097/01.mpg.0000421402.57633.4b. PMID 23103643. S2CID 21520744.
Ritz V, Alfalah M, Zimmer KP, Schmitz J, Jacob R, Naim HY (2003). "Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum". Gastroenterology. 125 (6): 1678–85. doi:10.1053/j.gastro.2003.09.022. PMID 14724820.
Spodsberg N, Jacob R, Alfalah M, Zimmer KP, Naim HY (2001). "Molecular basis of aberrant apical protein transport in an intestinal enzyme disorder" (PDF). J Biol Chem. 276 (26): 23506–10. doi:10.1074/jbc.c100219200. PMID 11340066.
Boney A, Elser HE, Silver HJ (2018). "Relationships among dietary intakes and persistent gastrointestinal symptoms in patients receiving enzyme treatment for genetic sucrase-isomaltase deficiency". J Acad Nutr Diet. 118 (3): 440–7. doi:10.1016/j.jand.2017.11.005. PMID 29311037.
Treem, William R. (2012). "Clinical Aspects and Treatment of Congenital Sucrase-Isomaltase Deficiency". Journal of Pediatric Gastroenterology and Nutrition. 55: S7–S13. doi:10.1097/01.mpg.0000421401.57633.90. PMID 23103658. S2CID 7179223.

gastrojournal.org

Alfalah M, Keiser M, Leeb T, Zimmer KP, Naim HY (2009). "Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency". Gastroenterology. 136 (3): 883–92. doi:10.1053/j.gastro.2008.11.038. PMID 19121318.
Ritz V, Alfalah M, Zimmer KP, Schmitz J, Jacob R, Naim HY (2003). "Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum". Gastroenterology. 125 (6): 1678–85. doi:10.1053/j.gastro.2003.09.022. PMID 14724820.

jbc.org

Keiser M, Alfalah M, Pröpsting MJ, Castelletti D, Naim HY (2006). "Altered folding, turnover, and polarized sorting act in concert to define a novel pathomechanism of congenital sucrase-isomaltase deficiency" (PDF). J Biol Chem. 281 (20): 14393–9. doi:10.1074/jbc.M513631200. PMID 16543230.
Spodsberg N, Jacob R, Alfalah M, Zimmer KP, Naim HY (2001). "Molecular basis of aberrant apical protein transport in an intestinal enzyme disorder" (PDF). J Biol Chem. 276 (26): 23506–10. doi:10.1074/jbc.c100219200. PMID 11340066.

nih.gov

pubmed.ncbi.nlm.nih.gov

Baudon JJ, Veinberg F, Thioulouse E, Morgant G, Aymard P, Charritat JL (April 1996). "Sucrase-isomaltase deficiency: changing pattern over two decades". J. Pediatr. Gastroenterol. Nutr. 22 (3): 284–8. doi:10.1097/00005176-199604000-00010. PMID 8708882.
Sander P, Alfalah M, Keiser M, et al. (January 2006). "Novel mutations in the human sucrase-isomaltase (SI) gene that cause congenital carbohydrate malabsorption". Hum. Mutat. 27 (1): 119. doi:10.1002/humu.9392. PMID 16329100.
Uhrich, Stefanie; Wu, Zaining; Huang, Jie-Yu; Scott, C. Ronald (2012). "Four Mutations in the SI Gene Are Responsible for the Majority of Clinical Symptoms of CSID". Journal of Pediatric Gastroenterology and Nutrition. 55: S34–5. doi:10.1097/01.mpg.0000421408.65257.b5. PMID 23103650. S2CID 747500.
Treem, William R. (1995). "Congenital sucrase-isomaltase deficiency". J Pediatr Gastroenterol Nutrition. 21 (21): 1–14. doi:10.1097/00005176-199507000-00001. PMID 8576798.
Gericke B, Amir M, Naim HY (2016). "The multiple roles of sucrase-isomaltase in the intestinal physiology". Mol Cell Pediatr. 3 (1): 2–6. doi:10.1186/s40348-016-0033-y. PMC 4728165. PMID 26812950.
Cohen, SA (2016). "The clinical consequences of sucrase-isomaltase deficiency". Mol Cell Pediatr. 3 (1): 5. doi:10.1186/s40348-015-0028-0. PMC 4746203. PMID 26857124.
Treem, WR (2012). "Clinical aspects and treatment of congenital sucrase-isomaltase deficiency" (PDF). Pediatr Gastroenterol Nutr. 55 (suppl 2): S7-13. doi:10.1097/01.mpg.0000421401.57633.90. PMID 23103658. S2CID 7179223. Archived from the original (PDF) on 2019-03-03.
Hackenmueller SA, Grenache DG (2016). "Reference intervals for intestinal disaccharidase activities determined from a non-reference population" (PDF). The Journal of Applied Laboratory Medicine. 1 (2): 172–80. doi:10.1373/jalm.2016.020388. PMID 33626784.
Puertolas MV, Fifi AC (2018). "The role of disaccharidase deficiencies in functional abdominal pain disorders—a narrative review". Nutrients. 10 (12): E1835. doi:10.3390/nu10121835. PMC 6315563. PMID 30501067.
Robayo-Torres CC, Quezada-Calvillo R, Nichols BL (2006). "Disaccharide digestion: clinical and molecular aspects". Clin Gastroenterol Hepatol. 4 (3): 276–87. doi:10.1016/j.cgh.2005.12.023. PMID 16527688.
Alfalah M, Keiser M, Leeb T, Zimmer KP, Naim HY (2009). "Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency". Gastroenterology. 136 (3): 883–92. doi:10.1053/j.gastro.2008.11.038. PMID 19121318.
Jacob R, Zimmer KP, Schmitz J, Naim HY (2000). "Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme". J Clin Invest. 106 (2): 281–7. doi:10.1172/JCI9677. PMC 314311. PMID 10903344.
Keiser M, Alfalah M, Pröpsting MJ, Castelletti D, Naim HY (2006). "Altered folding, turnover, and polarized sorting act in concert to define a novel pathomechanism of congenital sucrase-isomaltase deficiency" (PDF). J Biol Chem. 281 (20): 14393–9. doi:10.1074/jbc.M513631200. PMID 16543230.
Naim HY, Heine M, Zimmer KP (2012). "Congenital sucrase-isomaltase deficiency: heterogeneity of inheritance, trafficking, and function of an intestinal enzyme complex". J Pediatr Gastroenterol Nutr. 55 (suppl 2): S13-20. doi:10.1097/01.mpg.0000421402.57633.4b. PMID 23103643. S2CID 21520744.
Ritz V, Alfalah M, Zimmer KP, Schmitz J, Jacob R, Naim HY (2003). "Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum". Gastroenterology. 125 (6): 1678–85. doi:10.1053/j.gastro.2003.09.022. PMID 14724820.
Spodsberg N, Jacob R, Alfalah M, Zimmer KP, Naim HY (2001). "Molecular basis of aberrant apical protein transport in an intestinal enzyme disorder" (PDF). J Biol Chem. 276 (26): 23506–10. doi:10.1074/jbc.c100219200. PMID 11340066.
Boney A, Elser HE, Silver HJ (2018). "Relationships among dietary intakes and persistent gastrointestinal symptoms in patients receiving enzyme treatment for genetic sucrase-isomaltase deficiency". J Acad Nutr Diet. 118 (3): 440–7. doi:10.1016/j.jand.2017.11.005. PMID 29311037.
Treem, William R. (2012). "Clinical Aspects and Treatment of Congenital Sucrase-Isomaltase Deficiency". Journal of Pediatric Gastroenterology and Nutrition. 55: S7–S13. doi:10.1097/01.mpg.0000421401.57633.90. PMID 23103658. S2CID 7179223.

ncbi.nlm.nih.gov

Gericke B, Amir M, Naim HY (2016). "The multiple roles of sucrase-isomaltase in the intestinal physiology". Mol Cell Pediatr. 3 (1): 2–6. doi:10.1186/s40348-016-0033-y. PMC 4728165. PMID 26812950.
Cohen, SA (2016). "The clinical consequences of sucrase-isomaltase deficiency". Mol Cell Pediatr. 3 (1): 5. doi:10.1186/s40348-015-0028-0. PMC 4746203. PMID 26857124.
Puertolas MV, Fifi AC (2018). "The role of disaccharidase deficiencies in functional abdominal pain disorders—a narrative review". Nutrients. 10 (12): E1835. doi:10.3390/nu10121835. PMC 6315563. PMID 30501067.
Jacob R, Zimmer KP, Schmitz J, Naim HY (2000). "Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme". J Clin Invest. 106 (2): 281–7. doi:10.1172/JCI9677. PMC 314311. PMID 10903344.

semanticscholar.org

api.semanticscholar.org

Uhrich, Stefanie; Wu, Zaining; Huang, Jie-Yu; Scott, C. Ronald (2012). "Four Mutations in the SI Gene Are Responsible for the Majority of Clinical Symptoms of CSID". Journal of Pediatric Gastroenterology and Nutrition. 55: S34–5. doi:10.1097/01.mpg.0000421408.65257.b5. PMID 23103650. S2CID 747500.
Treem, WR (2012). "Clinical aspects and treatment of congenital sucrase-isomaltase deficiency" (PDF). Pediatr Gastroenterol Nutr. 55 (suppl 2): S7-13. doi:10.1097/01.mpg.0000421401.57633.90. PMID 23103658. S2CID 7179223. Archived from the original (PDF) on 2019-03-03.
Naim HY, Heine M, Zimmer KP (2012). "Congenital sucrase-isomaltase deficiency: heterogeneity of inheritance, trafficking, and function of an intestinal enzyme complex". J Pediatr Gastroenterol Nutr. 55 (suppl 2): S13-20. doi:10.1097/01.mpg.0000421402.57633.4b. PMID 23103643. S2CID 21520744.
Treem, William R. (2012). "Clinical Aspects and Treatment of Congenital Sucrase-Isomaltase Deficiency". Journal of Pediatric Gastroenterology and Nutrition. 55: S7–S13. doi:10.1097/01.mpg.0000421401.57633.90. PMID 23103658. S2CID 7179223.

pdfs.semanticscholar.org

Treem, WR (2012). "Clinical aspects and treatment of congenital sucrase-isomaltase deficiency" (PDF). Pediatr Gastroenterol Nutr. 55 (suppl 2): S7-13. doi:10.1097/01.mpg.0000421401.57633.90. PMID 23103658. S2CID 7179223. Archived from the original (PDF) on 2019-03-03.

sibotesting.com

Hamilton, LH (1998). "Breath Tests & Gastroenterology" (PDF). QuinTron Instrument Company Inc. Data on File.

web.archive.org

Treem, WR (2012). "Clinical aspects and treatment of congenital sucrase-isomaltase deficiency" (PDF). Pediatr Gastroenterol Nutr. 55 (suppl 2): S7-13. doi:10.1097/01.mpg.0000421401.57633.90. PMID 23103658. S2CID 7179223. Archived from the original (PDF) on 2019-03-03.