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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1991 | 1 |
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2019 | 1 |
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Page 1
Lactose and cataract in humans: a review.
J Am Coll Nutr. 1991 Feb;10(1):79-86. doi: 10.1080/07315724.1991.10718130.
J Am Coll Nutr. 1991.
PMID: 1901325
Review.
In these population groups, the size of which is unknown, the lens could be exposed to intermittent episodes of hypergalactosemia due to the presence of a partial enzyme deficiency in the galactose metabolic pathway, and/or the persistence of a high adult jejunal lactase a …
In these population groups, the size of which is unknown, the lens could be exposed to intermittent episodes of hypergalactosemia due …
Tendons Involvement in Congenital Metabolic Disorders.
Abate M, Salini V, Andia I.
Abate M, et al.
Adv Exp Med Biol. 2016;920:117-22. doi: 10.1007/978-3-319-33943-6_10.
Adv Exp Med Biol. 2016.
PMID: 27535253
Review.
Due to the accumulation of the homogentisic acid, tendons and ligaments are characterized by a typical ochre/yellow pigmentation (ochronosis), with ensuing inflammation, calcification and rupture. In Congenital Hypergalactosemia an increased tendon collagen cross-linking b …
Due to the accumulation of the homogentisic acid, tendons and ligaments are characterized by a typical ochre/yellow pigmentation (ochronosis …
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Galactose toxicity in animals.
Lai K, Elsas LJ, Wierenga KJ.
Lai K, et al.
IUBMB Life. 2009 Nov;61(11):1063-74. doi: 10.1002/iub.262.
IUBMB Life. 2009.
PMID: 19859980
Free PMC article.
Review.
In this contemporary review, we take a unique approach to present an overview of galactose toxicity resulting from the three known congenital disorders of galactose metabolism and from experimental hypergalactosemia. Additionally, we update the reader about research progre …
In this contemporary review, we take a unique approach to present an overview of galactose toxicity resulting from the three known congenita …
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The role of polyols in the pathophysiology of hypergalactosemia.
Berry GT.
Berry GT.
Eur J Pediatr. 1995;154(7 Suppl 2):S53-64. doi: 10.1007/BF02143805.
Eur J Pediatr. 1995.
PMID: 7671966
Review.
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Congenital extrahepatic portosystemic shunt: description of four cases and review of the literature.
Ponziani FR, Faccia M, Zocco MA, Giannelli V, Pellicelli A, Ettorre GM, De Matthaeis N, Pizzolante F, De Gaetano AM, Riccardi L, Pompili M, Rapaccini GL.
Ponziani FR, et al.
J Ultrasound. 2019 Sep;22(3):349-358. doi: 10.1007/s40477-018-0329-y. Epub 2018 Oct 24.
J Ultrasound. 2019.
PMID: 30357760
Free PMC article.
Review.
The diagnosis is frequently made during childhood in the setting of neonatal cholestasis, hypergalactosemia, failure to thrive, mental retardation or other congenital defects. ...
The diagnosis is frequently made during childhood in the setting of neonatal cholestasis, hypergalactosemia, failure to thrive, menta …
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