histidine has been researched along with Brain Disorders in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (62.50) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 2 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chien, HC; Colas, C; Giacomini, KM; Hall, C; Schlessinger, A; Thomas, AA; Wells, A; Wolfe, H | 1 |
| Ali, S; Gencoglu, H; Gozel, N; Hayirli, A; Komorowski, JR; Orhan, C; Ozkan, Y; Sahin, K; Sahin, N; Tuzcu, M | 1 |
| Brenner, C; Di Rocco, M; Leegwater, PA; Pronk, JC; Salvi, F; Storey, E; van Berkel, CG; van der Knaap, MS | 1 |
| Afting, EG; Bernhardt, W; Röthig, HJ | 1 |
| Brown, ES; Geison, RL; Gerritsen, T; Waisman, HA | 1 |
| Seegmiller, JE | 1 |
| Corner, BD; Holton, JB; Norman, RM; Williams, PM | 1 |
| Attal, C; Boisse, J; Lemonnier, A; Lévy, H; Mozziconacci, P | 1 |
1 review(s) available for histidine and Brain Disorders
| Article | Year |
|---|---|
Genetic and molecular basis of human hereditary diseases.
Topics: Amino Acid Metabolism, Inborn Errors; Arthritis; Brain Diseases; Genetic Diseases, Inborn; Glycogen Storage Disease; Gout; Histidine; Humans; Metabolism, Inborn Errors; Mutation; Nutrition Disorders; Phenylketonurias; Tyrosine | 1967 |
7 other study(ies) available for histidine and Brain Disorders
| Article | Year |
|---|---|
l-Type amino acid transporter 1 activity of 1,2,3-triazolyl analogs of l-histidine and l-tryptophan.
Topics: Antineoplastic Agents; Brain Diseases; Click Chemistry; Dose-Response Relationship, Drug; Histidine; Humans; Large Neutral Amino Acid-Transporter 1; Molecular Structure; Neoplasms; Prodrugs; Structure-Activity Relationship; Triazoles; Tryptophan | 2019 |
Chromium modulates expressions of neuronal plasticity markers and glial fibrillary acidic proteins in hypoglycemia-induced brain injury.
Topics: Animals; Blood Glucose; Brain; Brain Diseases; Cerebral Cortex; GAP-43 Protein; Glial Fibrillary Acidic Protein; Glucose Transporter Type 1; Glucose Transporter Type 3; Histidine; Hypoglycemia; Insulin; Male; Nerve Regeneration; Neural Cell Adhesion Molecules; Neuronal Plasticity; NF-E2-Related Factor 2; NF-kappa B; Organometallic Compounds; Picolinic Acids; Protective Agents; Rats; Rats, Sprague-Dawley | 2013 |
Arg113His mutation in eIF2Bepsilon as cause of leukoencephalopathy in adults.
Topics: Adult; Arginine; Brain; Brain Diseases; Demyelinating Diseases; Disease Progression; DNA Mutational Analysis; Eukaryotic Initiation Factor-2B; Female; Follow-Up Studies; Histidine; Homozygote; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Mutation | 2004 |
Excretion of total and muscular N tau-methylhistidine and creatinine in muscle diseases.
Topics: Adolescent; Adult; Brain Diseases; Creatinine; Female; Histidine; Humans; Male; Methylhistidines; Middle Aged; Muscular Diseases; Neuromuscular Diseases; Spinal Cord Diseases | 1984 |
Sibship with histidinemia and an unrelated encephalopathy. Clinical and biochemical studies.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Brain; Brain Diseases; Child; Child, Preschool; Female; Heart Defects, Congenital; Histidine; Humans; Imidazoles; Infant; Infant, Newborn; Intellectual Disability; Male; Obesity | 1977 |
A case of histidinemia controlled with a low histidine diet.
Topics: Amino Acid Metabolism, Inborn Errors; Blindness; Brain; Brain Damage, Chronic; Brain Diseases; Chromatography, Ion Exchange; Deafness; Diet Therapy; Dietary Proteins; Electrophoresis; Growth; Histidine; Humans; Infant; Intellectual Disability; Male; Serotonin | 1968 |
[Disorder of histidine metabolism induced by anticonvulsant therapy during a familial myoclonic encephalopathy].
Topics: Blindness; Brain Diseases; Child, Preschool; Female; Histidine; Humans; Infant; Infant, Newborn; Male; Metabolism, Inborn Errors; Myoclonus | 1964 |