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Adrenal cortex
Cerebellar cortex
Cerebellar impaction
Cerebellar impaction syndrome
Congenital cerebellar ataxia
Cortex cerebellaris
Cortex cerebelli
Cortex glandulae suprarenalis
Cortex of cerebellum.
Cortex of kidney
Cortex renalis
Cortex renis
Cortical substance of kidney
Lateral medullary syndrome
Marie disease
Marie's cerebellar ataxia
Marie's disease
Nonne-Marie sydrome
Posterior inferior cerebellar artery syndrome
Renal cortex
Substantia corticalis renis
Suprarenal cortex
Thrombosis of the posterior cerebellar artery
Vieusseux-Wallenberg syndrome
Wallenberg syndrome
Wallenberg's syndrome

Traduction de «Cerebellar cortex » (Anglais → Français) :

cerebellar cortex [ cortex of cerebellum. | cortex cerebelli | cortex cerebellaris ]

cortex cérébelleux [ écorce cérébelleuse | cortex cerebelli ]






renal cortex [ cortex of kidney | substantia corticalis renis | cortical substance of kidney | cortex renalis | cortex renis ]

cortex rénal [ cortex renalis ]


adrenal cortex [ suprarenal cortex | cortex glandulae suprarenalis ]

corticosurrénale [ cortex surrénal | cortex glandulae suprarenalis ]


Wallenberg's syndrome | lateral medullary syndrome | posterior inferior cerebellar artery syndrome | thrombosis of the posterior cerebellar artery | Vieusseux-Wallenberg syndrome | Wallenberg syndrome

syndrome de Wallenberg | syndrome de l'artère cérébelleuse postéro-inférieure | syndrome de l'artère latérale du bulbe | syndrome bulbaire latéral | syndrome rétro-olivaire de Déjerine | syndrome de Vieusseux-Wallenberg


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

rédo-ataxie cérébelleuse


cerebellar impaction | cerebellar impaction syndrome

syndrome d'engagement | syndrome d'engagement des amygdales cérébelleuses


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

ataxie type Caïman


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

ataxie spinocérébelleuse type 26


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