histidine has been researched along with Cerebellar Diseases in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Appleton, D; Coman, D; Jaeken, J; Klingberg, S; MacDonald, R; McGill, J; Morris, D | 1 |
| Bronzert, DA; Henkin, RI; Patten, BM; Re, PK | 1 |
2 other study(ies) available for histidine and Cerebellar Diseases
| Article | Year |
|---|---|
Congenital disorder of glycosylation type 1a: three siblings with a mild neurological phenotype.
Topics: Adult; Arginine; Ataxia; Cerebellar Diseases; Congenital Disorders of Glycosylation; Female; Histidine; Humans; Intellectual Disability; Lysine; Magnetic Resonance Imaging; Male; Mutation; Osteoporosis; Phenotype; Phosphotransferases (Phosphomutases); Siblings | 2007 |
A syndrome of acute zinc loss. Cerebellar dysfunction, mental changes, anorexia, and taste and smell dysfunction.
Topics: Adult; Anorexia; Cerebellar Diseases; Child; Female; Histidine; Humans; Mental Disorders; Metabolic Diseases; Middle Aged; Olfaction Disorders; Scleroderma, Systemic; Syndrome; Taste Disorders; Zinc | 1975 |