leucine has been researched along with Failure to Thrive in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Anzai, M; Aoki, Y; Endo, W; Haginoya, K; Inui, T; Kikuchi, A; Kure, S; Miyabayashi, T; Nagai, K; Niihori, T; Okubo, Y; Sato, R; Suzuki-Muromoto, S; Takezawa, Y; Togashi, N; Yamamura-Suzuki, S | 1 |
| Baumgartner, ER; Duran, M; Fingerhut, R; Kohlschütter, A; Lehnert, W; Steen, C; Stehn, M; Suormala, T | 1 |
| Koch, G; Mariman, E; Okhuijsen-Kroes, EJ; Sengers, RC; Smeitink, JA; Trijbels, JM; van den Heuvel, LP; Wendel, U | 1 |
1 review(s) available for leucine and Failure to Thrive
| Article | Year |
|---|---|
Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation.
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 |
2 other study(ies) available for leucine and Failure to Thrive
| Article | Year |
|---|---|
Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndrome.
Topics: Amino Acid Sequence; Child, Preschool; Ectodermal Dysplasia; Facies; Failure to Thrive; Heart Defects, Congenital; Humans; Leucine; Male; Proto-Oncogene Proteins B-raf; Sequence Deletion; Severity of Illness Index | 2019 |
Metabolic stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Carbon-Carbon Ligases; Carnitine; Diet, Protein-Restricted; Failure to Thrive; Female; Gliosis; Hemiplegia; Humans; Infant; Intellectual Disability; Leucine; Seizures | 1999 |