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8 in total

1. Effect of administration of the fructose on the glycogenolytic action of glucagon. An investigation of the pathogeny of hereditary fructose intolerance.

Authors: G Van Den Berghe; L Hue; H G Hers
Journal: Biochem J Date: 1973-06 Impact factor: 3.857

Review 2. Pharmaceutical excipients. Adverse effects associated with 'inactive' ingredients in drug products (Part II).

Authors: L K Golightly; S S Smolinske; M L Bennett; E W Sutherland; B H Rumack
Journal: Med Toxicol Adverse Drug Exp Date: 1988 May-Jun

3. Richard Gitzelmann (23rd February 1930--31st October 2013).

Authors: Beat Steinmann
Journal: Eur J Pediatr Date: 2014-04-27 Impact factor: 3.183

4. Hereditary tyrosinaemia. Clinical, enzymatic, and pathological study of an infant with the acute form of the disease.

Authors: N A Carson; J D Biggart; A H Bittles; D Donovan
Journal: Arch Dis Child Date: 1976-02 Impact factor: 3.791

5. Ketohexokinase C blockade ameliorates fructose-induced metabolic dysfunction in fructose-sensitive mice.

Authors: Miguel A Lanaspa; Ana Andres-Hernando; David J Orlicky; Christina Cicerchi; Cholsoon Jang; Nanxing Li; Tamara Milagres; Masanari Kuwabara; Michael F Wempe; Joshua D Rabinowitz; Richard J Johnson; Dean R Tolan
Journal: J Clin Invest Date: 2018-04-23 Impact factor: 14.808

Infantile lactic acidosis due to hereditary fructose 1,6-diphosphatase deficiency.

1. Effect of administration of the fructose on the glycogenolytic action of glucagon. An investigation of the pathogeny of hereditary fructose intolerance.

Review 2. Pharmaceutical excipients. Adverse effects associated with 'inactive' ingredients in drug products (Part II).

3. Richard Gitzelmann (23rd February 1930--31st October 2013).

4. Hereditary tyrosinaemia. Clinical, enzymatic, and pathological study of an infant with the acute form of the disease.

5. Ketohexokinase C blockade ameliorates fructose-induced metabolic dysfunction in fructose-sensitive mice.

6. Liver glycogen synthase deficiency: a rarely diagnosed entity.

7. Fructose and glucagon loading in siblings with fructose-1,6-diphosphatase deficiency in fed state.

8. Fructose-1,6-diphosphatase deficiency: glycerol excretion during fasting test.