Page last updated: 2024-10-27

gliclazide and Infant, Newborn, Diseases

gliclazide has been researched along with Infant, Newborn, Diseases in 2 studies

Gliclazide: An oral sulfonylurea hypoglycemic agent which stimulates insulin secretion.

Infant, Newborn, Diseases: Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Kelty, E1
Tran, DD1
Atkinson, A1
Preen, DB1
Havard, A1
Cho, JH1
Kang, E1
Lee, BH1
Kim, GH1
Choi, JH1
Yoo, HW1

Other Studies

2 other studies available for gliclazide and Infant, Newborn, Diseases

ArticleYear
Maternal and Neonatal Health Outcomes Associated with the Use of Gliclazide and Metformin for the Treatment of Diabetes in Pregnancy: A Record Linkage Study.
    Diabetes technology & therapeutics, 2020, Volume: 22, Issue:2

    Topics: Abnormalities, Drug-Induced; Adult; Diabetes, Gestational; Female; Gliclazide; Hospitalization; Huma

2020
DEND Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with Sulfonylurea.
    Journal of Korean medical science, 2017, Volume: 32, Issue:6

    Topics: Base Sequence; Brain; Diabetes Mellitus; DNA; Epilepsy; Gliclazide; Glycated Hemoglobin; Heterozygot

2017