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Results by year

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

Year Number of Results
1955 1
1957 1
1967 1
1970 3
1971 2
1972 3
1973 5
1974 1
1975 3
1976 3
1977 2
1978 3
1979 3
1981 1
1982 3
1983 3
1984 1
1985 5
1986 4
1988 3
1989 2
1990 1
1991 1
1992 3
1993 2
1995 5
1996 3
1997 3
1998 3
1999 2
2000 1
2001 3
2002 3
2003 6
2004 5
2005 4
2006 3
2007 2
2008 2
2009 2
2010 5
2011 4
2012 6
2013 4
2014 3
2015 5
2016 2
2017 1
2018 4
2019 3
2020 3
2021 3
2022 3
2023 1
2024 0

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Search Results

143 results

Results by year

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Quoted phrase not found in phrase index: "Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase"
Page 1
Galactose metabolism and health.
Coelho AI, Berry GT, Rubio-Gozalbo ME. Coelho AI, et al. Curr Opin Clin Nutr Metab Care. 2015 Jul;18(4):422-7. doi: 10.1097/MCO.0000000000000189. Curr Opin Clin Nutr Metab Care. 2015. PMID: 26001656 Review.
Gene therapy for human genetic disease?
Friedmann T, Roblin R. Friedmann T, et al. Science. 1972 Mar 3;175(4025):949-55. doi: 10.1126/science.175.4025.949. Science. 1972. PMID: 5061866
We therefore propose that a sustained effort be made to formulate a complete set of ethicoscientific criteria to guide the development and clinical application of gene therapy techniques. Such an endeavor could go a long way toward ensuring that gene therapy is used in hum …
We therefore propose that a sustained effort be made to formulate a complete set of ethicoscientific criteria to guide the development and …
Newborn screening for galactosaemia.
Lak R, Yazdizadeh B, Davari M, Nouhi M, Kelishadi R. Lak R, et al. Cochrane Database Syst Rev. 2017 Dec 23;12(12):CD012272. doi: 10.1002/14651858.CD012272.pub2. Cochrane Database Syst Rev. 2017. PMID: 29274129 Free PMC article. Updated. Review.
We also searched online trials registries and the reference lists of relevant articles and reviews.Date of the most recent search of Cochrane Cystic Fibrosis Group's Trials Register: 18 December 2017.Date of the most recent search of additional resources: 11 October 2017. SELECTI …
We also searched online trials registries and the reference lists of relevant articles and reviews.Date of the most recent search of Cochran …
Newborn screening for galactosaemia.
Lak R, Yazdizadeh B, Davari M, Nouhi M, Kelishadi R. Lak R, et al. Cochrane Database Syst Rev. 2020 Jun 22;6(6):CD012272. doi: 10.1002/14651858.CD012272.pub3. Cochrane Database Syst Rev. 2020. PMID: 32567677 Free PMC article.
Date of the most recent search of additional resources: 02 February 2020. SELECTION CRITERIA: Randomised controlled studies and controlled clinical studies, published or unpublished comparing the use of any newborn screening test to diagnose infants with galactosaem …
Date of the most recent search of additional resources: 02 February 2020. SELECTION CRITERIA: Randomised controlled studies and contr …
Circumstances when breastfeeding is contraindicated.
Lawrence RM. Lawrence RM. Pediatr Clin North Am. 2013 Feb;60(1):295-318. doi: 10.1016/j.pcl.2012.09.012. Epub 2012 Oct 30. Pediatr Clin North Am. 2013. PMID: 23178071 Review.
The molecular basis of galactosemia - Past, present and future.
Timson DJ. Timson DJ. Gene. 2016 Sep 10;589(2):133-41. doi: 10.1016/j.gene.2015.06.077. Epub 2015 Jul 2. Gene. 2016. PMID: 26143117 Review.
Initial studies concentrated on increasing the understanding of the clinical manifestations of the disease. However, Leloir's discovery of the pathway of galactose catabolism in the 1940s and 1950s enabled other scientists, notably Kalckar, to link the disease to a specifi …
Initial studies concentrated on increasing the understanding of the clinical manifestations of the disease. However, Leloir's discove …
Galactosemia and amenorrhea in the adolescent.
Berry GT. Berry GT. Ann N Y Acad Sci. 2008;1135:112-7. doi: 10.1196/annals.1429.038. Ann N Y Acad Sci. 2008. PMID: 18574215 Review.
The etiology of primary ovarian insufficiency (POI) in galactosemia is unknown. Clinical surveillance includes screening for abnormalities in ovarian function at an early age. ...
The etiology of primary ovarian insufficiency (POI) in galactosemia is unknown. Clinical surveillance includes screening for abnormal …
Innovative therapy for Classic Galactosemia - tale of two HTS.
Tang M, Odejinmi SI, Vankayalapati H, Wierenga KJ, Lai K. Tang M, et al. Mol Genet Metab. 2012 Jan;105(1):44-55. doi: 10.1016/j.ymgme.2011.09.028. Epub 2011 Oct 1. Mol Genet Metab. 2012. PMID: 22018723 Free PMC article. Review.
Soy infant formula: is it that bad?
Vandenplas Y, De Greef E, Devreker T, Hauser B. Vandenplas Y, et al. Acta Paediatr. 2011 Feb;100(2):162-6. doi: 10.1111/j.1651-2227.2010.02021.x. Epub 2010 Oct 13. Acta Paediatr. 2011. PMID: 20860705 Review.
143 results