Translation of "Cerebellar ataxia" in German

The characteristic feature of this inherited disease is cerebellar ataxia.

Later occur diplopia, nystagmus, vertigo, intention tremour, chanting speech, cerebellar ataxia.

Moreover, these bananas are produced in Ecuador by 10-year-old children who are paid USD 2 a day, who inhale pesticides, who have asthma, who have problems with their balance and who suffer from cerebellar ataxia.

We get him, boom, he's got tunnel vision, peripheral polyneuropathy, cerebellar ataxia, and now cardiomyopathy.

Cerebellar ataxia (incoordination and tremulous goal-directed movements of the limbs, gait unsteadiness, slurred speech) is difficult to control by drugs, however, all patients with parkinsonism should receive dopaminergic replacement therapy including levodopa and dopamine agonists since there is a 30% chance of benefit.

Older puppies show remarkable gait abnormalities – cerebellar ataxia (movement coordination ataxia), tremor, balance loss and associated movement abnormalities, such as eye movement disorder, loss of vision or behavioural disorders.

Their dysfunction and subsequent accumulation of waste material in their sacs causes a progressive cerebellar ataxia, altered function of degradation systems and neurodegeneration in affected individuals.

The potential effects of a high cumulative dose of metronidazole were uncovered as early as the 1970s with papers by Frytak, et al (1978), Halloran (1982) detailing neurological crises, cerebellar ataxia, seizures and altered mentation.

The SDCA2 is a subtype of a neurodegenerative disease known as spongy degeneration with cerebellar ataxia that affects Malinois dogs and other varieties of the Belgian shepherd breed.

The described mutation in GRM1 gene is associated with neonatal cerebellar ataxia (BNAt) in Coton de Tulear dogs.

Patients with late onset (over 40 years of age) tend to present with cerebellar ataxia, choreoathetosis and dementia.

Disease definition Machado-Joseph disease type 2 is a subtype of Machado-Joseph disease (SCA3/MJD, see this term) with intermediate severity characterized by an intermediate age of onset, cerebellar ataxia and external progressive ophthalmoplegia, with variable pyramidal and extrapyramidal signs.

All three types produce changes in limb coordination, but vestibular and cerebellar ataxia also produce changes in head and neck movement.

Cerebellar and pontine atrophy is visible with magnetic resonance imaging (MRI) in individuals who develop cerebellar ataxia.

Rare hereditary recessive disorder characterized by a pellagrous rash, cerebellar ataxia, mental retardation and renal aminoaciduria due to a defect in the cellular transport of neutral amino acids.

It ranges from experimental studies in animals to basic immunological and neurodegenerative mechanisms of MS and optic neuritis, cereobrospinal fluid analytical and imaging examination, immunoregulatory mechanisms in MS, the pathophysiology of auto antibody-mediated diseases of the CNS such as neuromyelitis optica (NMO) and autoimmune cerebellar ataxia, and experimental intervention studies in MS, NMO and brain tumors.