threonine has been researched along with Brain Disorders in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Bravo-Muñoz, M; de la Cruz, F; Garcés-Ramírez, L; Gómez-López, VM; Guadarrama-Ortíz, P; Harrington, CR; Hernandes-Alejandro, M; Luna-Muñoz, J; Martínez-Robles, S; Montiel-Sosa, F; Ontiveros-Torres, MÁ; Pacheco-Herrero, M; Villanueva-Fierro, I; Viramontes-Pintos, A; Yescas, P | 1 |
| Robertson, SP | 1 |
| Berge, T; Borgfors, N; Brun, A; von Studnitz, W | 1 |
3 other study(ies) available for threonine and Brain Disorders
| Article | Year |
|---|---|
Tau Protein Phosphorylated at Threonine-231 is Expressed Abundantly in the Cerebellum in Prion Encephalopathies.
Topics: Adult; Aged; Aged, 80 and over; Animals; Brain Diseases; Cattle; Cerebellum; Creutzfeldt-Jakob Syndrome; Encephalopathy, Bovine Spongiform; Female; Humans; Male; Middle Aged; Prion Diseases; tau Proteins; Threonine | 2021 |
Filamin a, periventricular nodular heterotopia, and West syndrome.
Topics: Brain Diseases; Cerebral Ventricles; Choristoma; Contractile Proteins; Developmental Disabilities; Electroencephalography; Exons; Female; Filamins; Genetic Diseases, X-Linked; Humans; Infant; Male; Methionine; Microfilament Proteins; Mutation; Mutation, Missense; Pedigree; Phenotype; Polymorphism, Single Nucleotide; Sequence Analysis, Protein; Spasms, Infantile; Threonine | 2006 |
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 |