threonine and Anemia, Cooley's

threonine has been researched along with Anemia, Cooley's in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's0 (0.00)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dadheech, S; Hussien, MD; Jain, S; Jyothy, A; Munshi, A; Rao, AV; Shaheen, U1
Falick, AM; Houston, ML; Lane, PA; McKinna, JD; Witkowska, HE1
Aoki, Y; Imai, K; Kikuchi, M; Kishikawa, M; Mawjood, AH; Miyazaki, A; Nakagawa, T; Nakanishi, T; Shimizu, A1

Other Studies

3 other study(ies) available for threonine and Anemia, Cooley's

ArticleYear
Three most common nonsynonymous UGT1A6*2 polymorphisms (Thr181Ala, Arg184Ser and Ser7Ala) and therapeutic response to deferiprone in β-thalassemia major patients.
    Gene, 2013, Dec-01, Volume: 531, Issue:2

    Topics: Adolescent; Alanine; Amino Acid Substitution; Arginine; beta-Thalassemia; Child; Child, Preschool; Deferiprone; Female; Gene Frequency; Genetic Association Studies; Glucuronosyltransferase; Humans; Iron Chelating Agents; Iron Overload; Isoenzymes; Male; Mutation, Missense; Polymorphism, Single Nucleotide; Pyridones; Serine; Threonine; Treatment Outcome

2013
Hemoglobin D Ibadan-beta zero thalassemia: detection by neonatal screening and confirmation by electrospray-ionization mass spectrometry.
    American journal of hematology, 1993, Volume: 44, Issue:3

    Topics: beta-Thalassemia; Globins; Hemoglobins, Abnormal; Humans; Infant, Newborn; Isoelectric Focusing; Lysine; Male; Mass Spectrometry; Neonatal Screening; Point Mutation; Threonine

1993
Compound heterozygosity for beta(+)-thalassemia [-31 (A-->G)] and a new variant with low oxygen affinity, Hb Sagami [beta139(H17)Asn-->Thr].
    Hemoglobin, 1999, Volume: 23, Issue:3

    Topics: Asparagine; Base Sequence; beta-Thalassemia; Hemoglobins, Abnormal; Heterozygote; Humans; Japan; Male; Mass Spectrometry; Middle Aged; Oxygen; Point Mutation; Polymerase Chain Reaction; Threonine

1999