Compounds > homocysteine

homocysteine and Infant, Newborn, Diseases

homocysteine has been researched along with Infant, Newborn, Diseases in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Blom, HJ; den Heijer, M; Gunnewiek, JK; Hogeveen, M; Ijland, M; Schonbeck, Y; van Oppenraaij, D1
Gokalp, AS; Turker, G; Usluer, H1
COFFEY, VP1
Dodelson de Kremer, R; Grosso, C1

Trials

1 trial(s) available for homocysteine and Infant, Newborn, Diseases

ArticleYear
The effect of folinic acid supplementation on homocysteine concentrations in newborns.
    European journal of clinical nutrition, 2010, Volume: 64, Issue:11

    Topics: Cerebrovascular Disorders; Dietary Supplements; Female; Folic Acid; Homocysteine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Leucovorin; Male; Prospective Studies; Risk Factors

2010

Other Studies

3 other study(ies) available for homocysteine and Infant, Newborn, Diseases

ArticleYear
Value of homocysteine levels, troponin I, and score for neonatal acute physiology and perinatal extension II as early predictors of morbidity.
    Pediatrics international : official journal of the Japan Pediatric Society, 2012, Volume: 54, Issue:1

    Topics: APACHE; Female; Fetal Blood; Homocysteine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Male; Pre-Eclampsia; Pregnancy; Prognosis; Regression Analysis; ROC Curve; Troponin I

2012
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
    Journal of the Irish Medical Association, 1964, Volume: 54

    Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency

1964
Maternal mutation 677C > T in the methylenetetrahydrofolate reductase gene associated with severe brain injury in offspring.
    Clinical genetics, 2005, Volume: 67, Issue:1

    Topics: Brain Damage, Chronic; Case-Control Studies; Child; Family Health; Female; Genotype; Homocysteine; Humans; Hypoxia-Ischemia, Brain; Infant, Newborn; Infant, Newborn, Diseases; Inheritance Patterns; Magnetic Resonance Imaging; Methylenetetrahydrofolate Reductase (NADPH2); Mothers; Pedigree; Point Mutation; Polymorphism, Single Nucleotide; Risk Factors

2005