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Acute cerebellar ataxia
Alcoholic cerebellar ataxia
Cerebral degeneration
Congenital cerebellar ataxia
Degeneration
Dysfunction of autonomic nervous system due to alcohol
Early-onset cerebellar ataxia
Early-onset cerebellar ataxia with essential tremor
Encephalopathy
Hunt's ataxia
Marie ataxia
Marie disease
Marie's ataxia
Marie's cerebellar ataxia
Marie's disease
Myoclonus
Nonne-Marie sydrome
Retained tendon reflexes

Vertaling van "Alcoholic cerebellar ataxia " (Engels → Nederlands) :

Alcoholic:cerebellar:ataxia | degeneration | cerebral degeneration | encephalopathy | Dysfunction of autonomic nervous system due to alcohol

alcoholische | cerebellaire | ataxie | alcoholische | cerebellaire | degeneratie | alcoholische | cerebrale degeneratie | alcoholische | encefalopathie | disfunctie van autonoom zenuwstelsel door alcoholgebruik


congenital cerebellar ataxia | Marie disease | Marie's cerebellar ataxia | Marie's disease | Nonne-Marie sydrome

erfelijke cerebellaire ataxie


Marie ataxia | Marie's ataxia | Marie's cerebellar ataxia

cerebellaire heredo-ataxie


A very rare subtype of autosomal dominant cerebellar ataxia type 3 with characteristics of late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on

spinocerebellaire ataxie type 26


Cerebellar ataxia Cayman type has characteristics of psychomotor retardation, hypotonia and cerebellar dysfunction (nystagmus, ataxic gait, truncal ataxia, dysarthric speech and intention tremor), associated with cerebellar hypoplasia. The prevalence

cerebellaire ataxie, Cayman-type


Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s

spinocerebellaire ataxie type 28


Early-onset cerebellar ataxia with:essential tremor | myoclonus [Hunt's ataxia] | retained tendon reflexes | Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia

Friedreich-ataxie (autosomaal recessief) | vroeg optredende cerebellaire ataxie met | behouden peesreflexen | vroeg optredende cerebellaire ataxie met | essentiële tremor | vroeg optredende cerebellaire ataxie met | myoclonus [Hunts ataxie] | recessieve spinocerebellaire ataxie, X-gebonden




Early-onset cerebellar ataxia

vroeg optredende cerebellaire ataxie




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'Alcoholic cerebellar ataxia' ->

Date index: 2023-01-24
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