leucine and Infant, Premature, Diseases

leucine has been researched along with Infant, Premature, Diseases in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
BAENS, GS; CORNBLATH, M; KLEIN, RI; WYBREGT, SH	1
Koch, G; Mariman, E; Okhuijsen-Kroes, EJ; Sengers, RC; Smeitink, JA; Trijbels, JM; van den Heuvel, LP; Wendel, U	1
Göpel, W; Kattner, E; Kohlmann, T; Möller, J; Segerer, H; Seidenberg, J	1
Hagge, W; Irtel von Brenndorff, A	1

Reviews

1 review(s) available for leucine and Infant, Premature, Diseases

Article	Year
Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation. Neuropediatrics, 2001, Volume: 32, Issue:4 Topics: Acidosis, Lactic; Child, Preschool; Diagnosis, Differential; DNA, Mitochondrial; Failure to Thrive; Fatal Outcome; Female; Humans; Infant; Infant, Newborn; Infant, Premature, Diseases; Leucine; Male; MELAS Syndrome; Mitochondrial Encephalomyopathies; Muscle Hypotonia; Muscle, Skeletal; Mutation; Phenotype	2001

Article

Year

Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation.

Neuropediatrics, 2001, Volume: 32, Issue:4

Topics: Acidosis, Lactic; Child, Preschool; Diagnosis, Differential; DNA, Mitochondrial; Failure to Thrive; Fatal Outcome; Female; Humans; Infant; Infant, Newborn; Infant, Premature, Diseases; Leucine; Male; MELAS Syndrome; Mitochondrial Encephalomyopathies; Muscle Hypotonia; Muscle, Skeletal; Mutation; Phenotype

2001

Other Studies

3 other study(ies) available for leucine and Infant, Premature, Diseases

Article	Year
SYMPTOMATIC NEONATAL HYPOGLYCEMIA. STUDIES OF CARBOHYDRATE METABOLISM IN THE NEWBORN INFANT. VIII. Pediatrics, 1964, Volume: 33 Topics: Adolescent; Black People; Blood Chemical Analysis; Carbohydrate Metabolism; Central Nervous System Diseases; Child; Diseases in Twins; Epinephrine; Female; Glucagon; Glucose Tolerance Test; Humans; Hypoglycemia; Infant; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature, Diseases; Leucine; Liver Glycogen; Neurologic Manifestations; Polycythemia; Pre-Eclampsia; Pregnancy; Tolbutamide	1964
The effect of the Val34Leu polymorphism in the factor XIII gene in infants with a birth weight below 1500 g. The Journal of pediatrics, 2002, Volume: 140, Issue:6 Topics: Alleles; Factor XIII; Female; Genotype; Gestational Age; Humans; Infant, Newborn; Infant, Premature; Infant, Premature, Diseases; Infant, Very Low Birth Weight; Intracranial Hemorrhages; Leucine; Leukomalacia, Periventricular; Logistic Models; Male; Mutation; Polymorphism, Genetic; Valine	2002
[Experiences with a new amino acid analyzer for a rapid analysis]. Monatsschrift fur Kinderheilkunde, 1970, Volume: 118, Issue:6 Topics: Amino Acids; Autoanalysis; Homocystine; Homocystinuria; Humans; Infant, Newborn; Infant, Premature, Diseases; Isoleucine; Leucine; Maple Syrup Urine Disease; Metabolic Diseases; Methionine; Phenylalanine; Phenylketonurias; Tyrosine; Valine	1970