isoleucine has been researched along with Developmental Disabilities in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 1 (25.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Dockter, G; Gomes, TS; Gortner, L; Leitner, D; Rohrer, T; Thakker, RV | 1 |
Clark, GD; Kim, J; O'Brien, WE; Sutton, VR; Wanders, RJ | 1 |
Ben-Omran, TI; Blaser, S; Callahan, J; Feigenbaum, A; Phillips, H | 1 |
Brown, GK; Danks, DM; Hunt, SM; Mitchell, DK | 1 |
4 other study(ies) available for isoleucine and Developmental Disabilities
Article | Year |
---|---|
HDR syndrome: a follow-up genotype-phenotype analysis of a de novo missense Thr272Ile mutation in exon 4 of GATA3.
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.
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.
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.
Topics: Amino Acid Metabolism, Inborn Errors; Developmental Disabilities; Dietary Proteins; Epilepsy; Female; Humans; Infant; Isoleucine; Muscle Hypotonia; Nervous System Diseases | 1987 |