Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
My NCBI Filters
Results by year

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

Year Number of Results
1968 2
1975 1
1976 1
1977 2
1978 2
1980 1
1981 2
1983 2
1984 1
1987 5
1988 1
1989 1
1990 6
1991 5
1992 1
1993 6
1994 2
1995 1
1996 3
1998 2
1999 3
2000 3
2002 2
2003 3
2004 1
2005 3
2006 3
2007 5
2008 2
2009 3
2010 3
2011 1
2012 2
2014 2
2015 4
2016 5
2017 2
2018 3
2019 6
2020 6
Text availability
Article attribute
Article type
Publication date

Similar Articles for PMID: 32709737

101 results
Results by year
Filters applied: . Clear all
Page 1
Pitfalls in the Diagnosis of Hereditary Fructose Intolerance.
Kim AY, Hughes JJ, Pipitone Dempsey A, Sondergaard Schatz K, Wang T, Gunay-Aygun M. Kim AY, et al. Pediatrics. 2020 Aug;146(2):e20193324. doi: 10.1542/peds.2019-3324. Pediatrics. 2020. PMID: 32709737
Hereditary Fructose Intolerance.
Baker P II, Ayres L, Gaughan S, Weisfeld-Adams J. Baker P II, et al. 2015 Dec 17. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 26677512 Free Books & Documents. Review.
Transferrin hypoglycosylation in hereditary fructose intolerance: using the clues and avoiding the pitfalls.
Adamowicz M, Płoski R, Rokicki D, Morava E, Gizewska M, Mierzewska H, Pollak A, Lefeber DJ, Wevers RA, Pronicka E. Adamowicz M, et al. J Inherit Metab Dis. 2007 Jun;30(3):407. doi: 10.1007/s10545-007-0569-z. Epub 2007 Apr 24. J Inherit Metab Dis. 2007. PMID: 17457694
The diagnosis of hereditary fructose intolerance.
Steinmann B, Gitzelmann R. Steinmann B, et al. Helv Paediatr Acta. 1981 Sep;36(4):297-316. Helv Paediatr Acta. 1981. PMID: 6268573
Acute liver failure in neonates with undiagnosed hereditary fructose intolerance due to exposure from widely available infant formulas.
Li H, Byers HM, Diaz-Kuan A, Vos MB, Hall PL, Tortorelli S, Singh R, Wallenstein MB, Allain M, Dimmock DP, Farrell RM, McCandless S, Gambello MJ. Li H, et al. Mol Genet Metab. 2018 Apr;123(4):428-432. doi: 10.1016/j.ymgme.2018.02.016. Epub 2018 Feb 27. Mol Genet Metab. 2018. PMID: 29510902
Isolation and characterization of a mutant liver aldolase in adult hereditary fructose intolerance. Identification of the enzyme variant by radioassay in tissue biopsy specimens.
Cox TM, O'Donnell MW, Camilleri M, Burghes AH. Cox TM, et al. J Clin Invest. 1983 Jul;72(1):201-13. doi: 10.1172/jci110958. J Clin Invest. 1983. PMID: 6348085 Free PMC article.
Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population.
Coffee EM, Yerkes L, Ewen EP, Zee T, Tolan DR. Coffee EM, et al. J Inherit Metab Dis. 2010 Feb;33(1):33-42. doi: 10.1007/s10545-009-9008-7. Epub 2009 Dec 23. J Inherit Metab Dis. 2010. PMID: 20033295 Free PMC article.
Kidney and vascular function in adult patients with hereditary fructose intolerance.
Simons N, Debray FG, Schaper NC, Feskens EJM, Hollak CEM, Bons JAP, Bierau J, Houben AJHM, Schalkwijk CG, Stehouwer CDA, Cassiman D, Brouwers MCGJ. Simons N, et al. Mol Genet Metab Rep. 2020 May 11;23:100600. doi: 10.1016/j.ymgmr.2020.100600. eCollection 2020 Jun. Mol Genet Metab Rep. 2020. PMID: 32426234 Free PMC article.
Aldolase-B knockout in mice phenocopies hereditary fructose intolerance in humans.
Oppelt SA, Sennott EM, Tolan DR. Oppelt SA, et al. Mol Genet Metab. 2015 Mar;114(3):445-50. doi: 10.1016/j.ymgme.2015.01.001. Epub 2015 Jan 22. Mol Genet Metab. 2015. PMID: 25637246
Hereditary fructose intolerance: functional study of two novel ALDOB natural variants and characterization of a partial gene deletion.
Esposito G, Imperato MR, Ieno L, Sorvillo R, Benigno V, Parenti G, Parini R, Vitagliano L, Zagari A, Salvatore F. Esposito G, et al. Hum Mutat. 2010 Dec;31(12):1294-303. doi: 10.1002/humu.21359. Epub 2010 Nov 16. Hum Mutat. 2010. PMID: 20848650
101 results
Jump to page
Feedback