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

Year Number of Results
1976 2
1978 2
1979 1
1982 1
1988 1
1993 1
1994 1
1995 1
1996 1
1997 1
1998 1
2001 1
2010 1
2012 1
2022 0
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16 results
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Page 1
Disorders of gluconeogenesis.
van den Berghe G. van den Berghe G. J Inherit Metab Dis. 1996;19(4):470-7. doi: 10.1007/BF01799108. J Inherit Metab Dis. 1996. PMID: 8884571 Review.
Inborn deficiencies are known of each of the four enzymes of the glycolytic-gluconeogenic pathway that ensure a unidirectional flux from pyruvate to glucose: pyruvate carboxylase, phosphoenolpyruvate carboxykinase, fructose-1,6-bisphosphatase, and glucose- …
Inborn deficiencies are known of each of the four enzymes of the glycolytic-gluconeogenic pathway that ensure a unidirectional flux from pyr …
Inborn errors of carbohydrate metabolism.
Mayatepek E, Hoffmann B, Meissner T. Mayatepek E, et al. Best Pract Res Clin Gastroenterol. 2010 Oct;24(5):607-18. doi: 10.1016/j.bpg.2010.07.012. Best Pract Res Clin Gastroenterol. 2010. PMID: 20955963 Review.
Glycogen storage diseases (GSD) and inborn errors of galactose and fructose metabolism are the most common representatives of inborn errors of carbohydrate metabolism. ...A lactose-free infant formula can be life-saving in affected neonates whereas a strict fructose
Glycogen storage diseases (GSD) and inborn errors of galactose and fructose metabolism are the most common representatives of inborn …
Hypoglycaemia related to inherited metabolic diseases in adults.
Douillard C, Mention K, Dobbelaere D, Wemeau JL, Saudubray JM, Vantyghem MC. Douillard C, et al. Orphanet J Rare Dis. 2012 May 15;7:26. doi: 10.1186/1750-1172-7-26. Orphanet J Rare Dis. 2012. PMID: 22587661 Free PMC article. Review.
Exercise-induced hyperinsulinism is linked to an activating mutation of the monocarboxylate transporter 1 (one family). Fasting hypoglycaemia may be caused by IEM that were already diagnosed in childhood and persist into adulthood: glycogen storage disease (GSD) type I, II …
Exercise-induced hyperinsulinism is linked to an activating mutation of the monocarboxylate transporter 1 (one family). Fasting hypog …
Inborn errors of fructose metabolism.
Hommes FA. Hommes FA. Am J Clin Nutr. 1993 Nov;58(5 Suppl):788S-795S. doi: 10.1093/ajcn/58.5.788S. Am J Clin Nutr. 1993. PMID: 8213611 Review.
A review is presented of genetic defects affecting fructose metabolism in humans. Presently, six conditions have been recognized: fructose malabsorption, fructokinase deficiency, aldolase A and aldolase B deficiency, fructose-1,6- …
A review is presented of genetic defects affecting fructose metabolism in humans. Presently, six conditions have been recognized: …
[Fructose-1,6-bisphosphatase deficiency].
Sakamoto O, Ohura T. Sakamoto O, et al. Ryoikibetsu Shokogun Shirizu. 2001;(33):726-8. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462656 Review. Japanese. No abstract available.
[Fructose-1,6-bisphosphatase deficiency].
Nakamura N, Kamoda T. Nakamura N, et al. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):88-91. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9589997 Review. Japanese. No abstract available.
Lactic acidosis in childhood.
Israels S, Haworth JC, Dunn HG, Applegarth DA. Israels S, et al. Adv Pediatr. 1976;22:267-303. Adv Pediatr. 1976. PMID: 178159 Review.
Children with chronic metabolic acidosis should be investigated to determine the presence of an organic acid, especially when the plasma electrolyte profile shows a deficiency of anion. One of the organic acids that should be looked for in such a patient is lactic acid. .. …
Children with chronic metabolic acidosis should be investigated to determine the presence of an organic acid, especially when the plasma ele …
Hepatic Disorders.
Mowat AP. Mowat AP. Clin Gastroenterol. 1982 Jan;11(1):171-205. Clin Gastroenterol. 1982. PMID: 6277534 Review. No abstract available.
[Enzymopathic congenital hyperlactacidemia].
Leroux JP, Marsac C, Saudubray JM. Leroux JP, et al. Ann Biol Clin (Paris). 1976;34(2):151-9. Ann Biol Clin (Paris). 1976. PMID: 184725 Review. French.
Congenital enzymopathic hyperlactacidemia results from a defect of utilisation of pyruvate either at the level of the pyruvate junction (pyruvate-carboxylase, pyruvate-dehydrogenase and Kreb's cycle), or at the level of the unidirectional enzymes on neo-glucogenesis and of neo-gl …
Congenital enzymopathic hyperlactacidemia results from a defect of utilisation of pyruvate either at the level of the pyruvate junction (pyr …
Inborn errors of fructose metabolism.
Van den Berghe G. Van den Berghe G. Annu Rev Nutr. 1994;14:41-58. doi: 10.1146/annurev.nu.14.070194.000353. Annu Rev Nutr. 1994. PMID: 7946527 Review. No abstract available.
16 results