Page last updated: 2024-10-21

phenytoin and Glycogen Storage Disease

phenytoin has been researched along with Glycogen Storage Disease in 3 studies

Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19903 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Walson, P1
Trinca, C1
Bressler, R1
Brown, BI1
Jubiz, W1
Rallison, ML1

Other Studies

3 other studies available for phenytoin and Glycogen Storage Disease

ArticleYear
New uses for phenytoin.
    JAMA, 1975, Sep-29, Volume: 233, Issue:13

    Topics: Arrhythmias, Cardiac; Diabetic Neuropathies; Digitalis Glycosides; Drug Evaluation; Epilepsy; Gastro

1975
Diphenylhydantoin treatment.
    Archives of internal medicine, 1975, Volume: 135, Issue:5

    Topics: Glycogen Storage Disease; Humans; Phenytoin

1975
Diphenylhydantoin treatment of glycogen storage diseases.
    Archives of internal medicine, 1974, Volume: 134, Issue:3

    Topics: Adolescent; Adult; Child; Child, Preschool; Female; Glucose-6-Phosphatase; Glucosidases; Glucosyltra

1974