isoleucine and Developmental Disabilities

isoleucine has been researched along with Developmental Disabilities in 4 studies

Research

Studies (4)

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

Authors

AuthorsStudies
Dockter, G; Gomes, TS; Gortner, L; Leitner, D; Rohrer, T; Thakker, RV1
Clark, GD; Kim, J; O'Brien, WE; Sutton, VR; Wanders, RJ1
Ben-Omran, TI; Blaser, S; Callahan, J; Feigenbaum, A; Phillips, H1
Brown, GK; Danks, DM; Hunt, SM; Mitchell, DK1

Other Studies

4 other study(ies) available for isoleucine and Developmental Disabilities

ArticleYear
HDR syndrome: a follow-up genotype-phenotype analysis of a de novo missense Thr272Ile mutation in exon 4 of GATA3.
    Klinische Padiatrie, 2012, Volume: 224, Issue:7

    Topics: Child; Child, Preschool; Combined Modality Therapy; Developmental Disabilities; DNA Mutational Analysis; Exons; Follow-Up Studies; GATA3 Transcription Factor; Genetic Carrier Screening; Genotype; Hearing Loss, Sensorineural; Humans; Hypoparathyroidism; Infant; Isoleucine; Male; Mutation, Missense; Nephrosis; Phenotype; Threonine

2012
3-Hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency.
    Journal of inherited metabolic disease, 2003, Volume: 26, Issue:1

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acids; Alcohol Oxidoreductases; Blindness, Cortical; Developmental Disabilities; Diet, Protein-Restricted; Epilepsies, Myoclonic; Humans; Infant; Isoleucine; Male; Metabolism, Inborn Errors

2003
Atypical phenotype in a boy with a maple syrup urine disease.
    Journal of inherited metabolic disease, 2006, Volume: 29, Issue:1

    Topics: Amino Acids, Branched-Chain; Brain; Cerebellum; Developmental Disabilities; Humans; Infant; Intellectual Disability; Isoleucine; Male; Maple Syrup Urine Disease; Phenotype

2006
Profound neurological illness, relieved by protein restriction, in a baby with a transient disturbance in the metabolism of ingested isoleucine.
    European journal of pediatrics, 1987, Volume: 146, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Developmental Disabilities; Dietary Proteins; Epilepsy; Female; Humans; Infant; Isoleucine; Muscle Hypotonia; Nervous System Diseases

1987