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Select item 110790811.

Inactivation of Escherichia coli, Salmonella enterica, and Listeria monocytogenes using the Contamination Sanitization Inspection and Disinfection (CSI-D) device

Jennifer McCoy Sanders, Vanessa Alarcon, Grace Marquis, Amanda Tabb, Jo Ann Van Kessel, Jakeitha Sonnier, Bradd J. Haley, Insuck Baek, Jianwei Qin, Moon Kim, Fartash Vasefi, Stanislav Sokolov, Rosalee S. Hellberg

Heliyon. 2024 May 15; 10(9): e30490. Published online 2024 Apr 29. doi: 10.1016/j.heliyon.2024.e30490

PMCID:: PMC11079081

Abstract Article PDF–706K

Select item 108550312.

A Comparative Study of Three Dementia Screening Instruments (CSI-D, CMMSE, and ECAQ) in a Multi-Ethnic Asian Population

Narayanaswamy Venketasubramanian

Healthcare (Basel) 2024 Feb; 12(3): 410. Published online 2024 Feb 5. doi: 10.3390/healthcare12030410

PMCID:: PMC10855031

Abstract Article PDF–229K

Select item 99702173.

The effect of sucrase-isomaltase deficiency on metabolism, food intake and preferences: protocol for a dietary intervention study

Ninna Karsbæk Senftleber, Kristine Skøtt Pedersen, Cecilie Schnoor Jørgensen, Hanne Pedersen, Marie Mathilde Bjerg Christensen, Emilie Kabel Madsen, Kristine Andersen, Emil Jørsboe, Matthew Paul Gillum, Michael Bom Frøst, Torben Hansen, Marit Eika Jørgensen

Int J Circumpolar Health. 2023; 82(1): 2178067. Published online 2023 Feb 22. doi: 10.1080/22423982.2023.2178067

PMCID:: PMC9970217

Abstract Article PDF–1014K

Select item 86755674.

Two Novel Mutations in the SI Gene Associated With Congenital Sucrase-Isomaltase Deficiency: A Case Report in China

Jianli Zhou, Yuzhen Zhao, Xia Qian, Yongwei Cheng, Huabo Cai, Moxian Chen, Shaoming Zhou

Front Pediatr. 2021; 9: 731716. Published online 2021 Dec 2. doi: 10.3389/fped.2021.731716

PMCID:: PMC8675567

Abstract Article PDF–2.0M

Select item 82982465.

The patient journey to diagnosis and treatment of congenital sucrase-isomaltase deficiency

Heather Smith, Beverly Romero, Emuella Flood, Anne Boney

Qual Life Res. 2021; 30(8): 2329–2338. Published online 2021 Mar 27. doi: 10.1007/s11136-021-02819-z

PMCID:: PMC8298246

Abstract Article PDF–543K

Select item 81768896.

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

Yael Haberman, Ayelet Di Segni, Nurit Loberman-Nachum, Ortal Barel, Vered Kunik, Eran Eyal, Nitzan Kol, Goni Hout-Siloni, Brigitte Kochavi, Camila Avivi, Michael Schvimer, Gideon Rechavi, Yair Anikster, Iris Barshack, Batia Weiss

J Pediatr Gastroenterol Nutr. Author manuscript; available in PMC 2021 Jun 4.

Published in final edited form as: J Pediatr Gastroenterol Nutr. 2017 May; 64(5): 770–776. doi: 10.1097/MPG.0000000000001424

PMCID:: PMC8176889

Abstract Article PDF–1.7M

Select item 81052317.

Sucrase-Isomaltase Deficiency Causing Persistent Bloating and Diarrhea in an Adult Female

Varsha Chiruvella, Ayesha Cheema, Hafiz Muhammad Sharjeel Arshad, Jacqueline T Chan, John Erikson L Yap

Cureus. 2021 Apr; 13(4): e14349. Published online 2021 Apr 7. doi: 10.7759/cureus.14349

PMCID:: PMC8105231

Abstract Article PDF–320K

Select item 78221258.

Differential Effects of Sucrase-Isomaltase Mutants on Its Trafficking and Function in Irritable Bowel Syndrome: Similarities to Congenital Sucrase-Isomaltase Deficiency

Diab M. Husein, Sandra Rizk, Hassan Y. Naim

Nutrients. 2021 Jan; 13(1): 9. Published online 2020 Dec 22. doi: 10.3390/nu13010009

PMCID:: PMC7822125

Abstract Article PDF–1.0M

Select item 76943459.

CSID: A Novel Multimodal Image Fusion Algorithm for Enhanced Clinical Diagnosis

Shah Rukh Muzammil, Sarmad Maqsood, Shahab Haider, Robertas Damaševičius

Diagnostics (Basel) 2020 Nov; 10(11): 904. Published online 2020 Nov 5. doi: 10.3390/diagnostics10110904

PMCID:: PMC7694345

Abstract Article PDF–3.3M

Select item 713299410.

Glutarate L-2-Hydroxylase (CsiD/GlaH) is an Archetype Fe(II)/2-Oxoglutarate-Dependent Dioxygenase

Caitlyn Q Herr, Lee Macomber, Efthalia Kalliri, Robert P. Hausinger

Adv Protein Chem Struct Biol. Author manuscript; available in PMC 2020 Jun 10.

Published in final edited form as: Adv Protein Chem Struct Biol. 2019; 117: 63–90. Published online 2019 Jun 10. doi: 10.1016/bs.apcsb.2019.05.001

PMCID:: PMC7132994

Abstract Article PDF–2.1M

Select item 683586011.

Heterozygotes Are a Potential New Entity among Homozygotes and Compound Heterozygotes in Congenital Sucrase-Isomaltase Deficiency

Diab M. Husein, Dalanda Wanes, Lara M. Marten, Klaus-Peter Zimmer, Hassan Y. Naim

Nutrients. 2019 Oct; 11(10): 2290. Published online 2019 Sep 25. doi: 10.3390/nu11102290

PMCID:: PMC6835860

Abstract Article PDF–1001K

Select item 595729112.

¹³C-Labeled-Starch Breath Test in Congenital Sucrase-Isomaltase Deficiency

Claudia C Robayo-Torres, Marisela Diaz-Sotomayor, Bruce R Hamaker, Susan S. Baker, Bruno P Chumpitazi, Antone R. Opekun, Buford L. Nichols

J Pediatr Gastroenterol Nutr. Author manuscript; available in PMC 2019 Jun 1.

Published in final edited form as: J Pediatr Gastroenterol Nutr. 2018 Jun; 66(Suppl 3): S61–S64. doi: 10.1097/MPG.0000000000001858

PMCID:: PMC5957291

Abstract Article PDF–389K

Select item 474620313.

The clinical consequences of sucrase-isomaltase deficiency

Stanley A. Cohen

Mol Cell Pediatr. 2016 Dec; 3: 5. Published online 2016 Feb 8. doi: 10.1186/s40348-015-0028-0

PMCID:: PMC4746203

Abstract Article PDF–570K

Select item 431214814.

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

Julien L. Marcadier, Margaret Boland, C. Ronald Scott, Kheirie Issa, Zaining Wu, Adam D. McIntyre, Robert A. Hegele, Michael T. Geraghty, Matthew A. Lines

CMAJ. 2015 Feb 3; 187(2): 102–107. doi: 10.1503/cmaj.140657