halothane has been researched along with Pantothenate Kinase-Associated Neurodegeneration in 1 studies
Pantothenate Kinase-Associated Neurodegeneration: A rare autosomal recessive degenerative disorder which usually presents in late childhood or adolescence. Clinical manifestations include progressive MUSCLE SPASTICITY; hyperreflexia; MUSCLE RIGIDITY; DYSTONIA; DYSARTHRIA; and intellectual deterioration which progresses to severe dementia over several years. (From Adams et al., Principles of Neurology, 6th ed, p972; Davis & Robertson, Textbook of Neuropathology, 2nd ed, pp972-929)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Roy, RC | 1 |
| McLain, S | 1 |
| Wise, A | 1 |
| Shaffner, LD | 1 |
1 other study available for halothane and Pantothenate Kinase-Associated Neurodegeneration
| Article | Year |
|---|---|
Anesthetic management of a patient with Hallervorden-Spatz disease.
Topics: Adult; Anesthesia, Inhalation; Basal Ganglia Diseases; Female; Halothane; Humans; Intubation, Gastro | 1983 |