carnitine has been researched along with Cerebellar Ataxia in 2 studies
Cerebellar Ataxia: Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Auré, K | 1 |
| Benoist, JF | 1 |
| Ogier de Baulny, H | 1 |
| Romero, NB | 1 |
| Rigal, O | 1 |
| Lombès, A | 1 |
| Tóth, G | 1 |
| Morava, E | 1 |
| Bene, J | 1 |
| Selhorst, JJ | 1 |
| Overmars, H | 1 |
| Vreken, P | 1 |
| Molnár, J | 1 |
| Farkas, V | 1 |
| Melegh, B | 1 |
2 other studies available for carnitine and Cerebellar Ataxia
| Article | Year |
|---|---|
Progression despite replacement of a myopathic form of coenzyme Q10 defect.
Topics: Benzoquinones; Carnitine; Cerebellar Ataxia; Cerebellum; Child, Preschool; Disease Progression; Drug | 2004 |
Carnitine-responsive carnitine insufficiency in a case of mtDNA 8993T>C mutation associated Leigh syndrome.
Topics: Carnitine; Cerebellar Ataxia; Child; DNA, Mitochondrial; Humans; Intellectual Disability; Leigh Dise | 2001 |