threonine has been researched along with Infant, Premature, Diseases in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (66.67) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Haataja, R; Hallman, M; Huusko, JM; Karjalainen, MK; Luukkonen, A; Tuohimaa, A | 1 |
Bernini, LF; Camaschella, C; Mazza, U; Pich, PG; Ricco, G; Saglio, G; Turi, RM | 1 |
Berge, T; Borgfors, N; Brun, A; von Studnitz, W | 1 |
3 other study(ies) available for threonine and Infant, Premature, Diseases
Article | Year |
---|---|
A study of collectin genes in spontaneous preterm birth reveals an association with a common surfactant protein D gene polymorphism.
Topics: Adolescent; Adult; Collectins; Female; Genetic Predisposition to Disease; Gestational Age; Haplotypes; Humans; Infant, Newborn; Infant, Premature; Infant, Premature, Diseases; Linkage Disequilibrium; Mannose-Binding Lectin; Methionine; Middle Aged; Polymorphism, Genetic; Pregnancy; Premature Birth; Pulmonary Surfactant-Associated Protein A; Pulmonary Surfactant-Associated Protein D; Threonine; Young Adult | 2012 |
Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine replaced by threonine at position 75 )E 19) of the gamma chain.
Topics: Adult; Amino Acid Sequence; Anemia, Aplastic; Child; Fetal Blood; Fetal Hemoglobin; Genes; Hemoglobins, Abnormal; Homozygote; Humans; Infant, Newborn; Infant, Premature; Infant, Premature, Diseases; Isoleucine; Pedigree; Thalassemia; Threonine | 1976 |
Encephalopathy in combination with a new pattern of aminoaciduria.
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Central Nervous System; Chromatography; Cyanosis; Dyspnea, Paroxysmal; Electroencephalography; Exchange Transfusion, Whole Blood; Humans; Hyperbilirubinemia; Infant; Infant, Newborn; Infant, Premature, Diseases; Male; Serine; Spectrophotometry; Threonine | 1969 |