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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1967 1
1971 1
1972 1
1973 2
1974 2
1976 4
1977 1
1978 1
1979 1
1980 3
1981 3
1982 3
1983 3
1984 2
1985 2
1986 1
1987 3
1988 4
1989 2
1990 2
1991 3
1993 2
1995 2
1996 6
1997 3
1998 5
1999 2
2000 2
2001 3
2002 1
2003 3
2004 1
2006 2
2008 3
2009 3
2012 12
2014 2
2015 4
2016 3
2017 4
2018 6
2019 10
2020 7
Text availability
Article attribute
Article type
Publication date

Similar Articles for PMID: 25452324

125 results
Results by year
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Page 1
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. Marcadier JL, et al. CMAJ. 2015 Feb 3;187(2):102-107. doi: 10.1503/cmaj.140657. Epub 2014 Dec 1. CMAJ. 2015. PMID: 25452324 Free PMC article.
Old meets new: identifying founder mutations in genetic disease.
Evans JA. Evans JA. CMAJ. 2015 Feb 3;187(2):93-94. doi: 10.1503/cmaj.141509. Epub 2015 Jan 19. CMAJ. 2015. PMID: 25602001 Free PMC article. No abstract available.
Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients.
Gericke B, Amiri M, Scott CR, Naim HY. Gericke B, et al. Biochim Biophys Acta Mol Basis Dis. 2017 Mar;1863(3):817-826. doi: 10.1016/j.bbadis.2016.12.017. Epub 2017 Jan 3. Biochim Biophys Acta Mol Basis Dis. 2017. PMID: 28062276 Free article.
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. Haberman Y, et al. J Pediatr Gastroenterol Nutr. 2017 May;64(5):770-776. doi: 10.1097/MPG.0000000000001424. J Pediatr Gastroenterol Nutr. 2017. PMID: 27749612
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. Belmont JW, et al. BMC Pediatr. 2002 Apr 25;2:4. doi: 10.1186/1471-2431-2-4. BMC Pediatr. 2002. PMID: 12014995 Free PMC article.
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. Alfalah M, et al. Gastroenterology. 2009 Mar;136(3):883-92. doi: 10.1053/j.gastro.2008.11.038. Epub 2008 Nov 19. Gastroenterology. 2009. PMID: 19121318
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. Henström M, et al. Gut. 2018 Feb;67(2):263-270. doi: 10.1136/gutjnl-2016-312456. Epub 2016 Nov 21. Gut. 2018. PMID: 27872184 Free PMC article. Clinical Trial.
Congenital sucrase-isomaltase deficiency.
Treem WR. Treem WR. J Pediatr Gastroenterol Nutr. 1995 Jul;21(1):1-14. doi: 10.1097/00005176-199507000-00001. J Pediatr Gastroenterol Nutr. 1995. PMID: 8576798 Review. No abstract available.
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