(Q41870578)

13 October 2017

Iatrogenic deaths in hereditary fructose intolerance (English)

1 reference

13 October 2017

Cox TM

1

1 reference

PMC publication ID

1029544

13 October 2017

language of work or name

English

0 references

publication date

1 October 1993

1 reference

Archives of Disease in Childhood

13 October 2017

1 reference

13 October 2017

69

1 reference

13 October 2017

4

1 reference

13 October 2017

413-415

1 reference

Fructose in the treatment of diabetic ketosis

13 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

DNA diagnosis of fatal fructose intolerance from archival tissue

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Fatal liver dystrophy in 3 siblings with hereditary fructose intolerance after long-lasting infusion with sorbitol solutions

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Hereditary fructose intolerance: report of a case and comments on the hazards of fructose infusion

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Study of hereditary fructose intolerance by use of 31P magnetic resonance spectroscopy

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Molecular analysis of aldolase B genes in the diagnosis of hereditary fructose intolerance in the United Kingdom.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Molecular analysis of aldolase B genes in hereditary fructose intolerance

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Hereditary fructose intolerance in early childhood: a major diagnostic challenge. Survey of 20 symptomatic cases

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Hereditary fructose intolerance in childhood. Diagnosis, management, and course in 55 patients

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Hereditary fructose intolerance: A difficult diagnosis in the adult

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Postoperative fructose infusion in a case of presumed hereditary fructose intolerance (author's transl)

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1029544

Pseudodominant transmission of fructose intolerance in an adult and three offspring: Heterozygote detection by intestinal biopsy

5 June 2018

1 reference

12 December 2020

[Death following fructose and sorbitol infusions]

1 reference

12 December 2020

Chronic fructose intoxication after infancy in children with hereditary fructose intolerance. A cause of growth retardation

1 reference

12 December 2020

Mechanism of folate deficiency in patients receiving phenytoin

1 reference

12 December 2020

[Study of a case of functional hypoglycemia caused by intolerance to fructose.]

1 reference

12 December 2020

Lactic acid accumulation in connection with fructose infusion

1 reference

12 December 2020

Use of glucose, invert sugar and fructose for parenteral feeding of children

1 reference

12 December 2020

An experimental renal acidification defect in patients with hereditary fructose intolerance. II. Its distinction from classic renal tubular acidosis; its resemblance to the renal acidification defect associated with the Fanconi syndrome of children

1 reference

12 December 2020

IDIOSYNCRASY TO FRUCTOSE

1 reference

12 December 2020

Hereditary fructose intolerance. Dental status of eight patients

1 reference

12 December 2020

[Discovery of fructose intolerance in a case of acute liver failure in a 16-month-old child]

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.69.4.413

1 reference

13 October 2017

1 reference

PMC publication ID

1029544

13 October 2017

PubMed publication ID

8259868

1 reference

PMC publication ID

1029544