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Acromegalia
Acromegaly
Congenital cerebellar ataxia
Familiar ataxia
Friedreich disease
Friedreich familial ataxia
Friedreich hereditary ataxia
Friedreich hereditary spinal ataxia
Friedreich spinocerebella
Friedreich's ataxia
Friedreich's disease
Friedreich's familial ataxia
Friedreich's hereditary ataxia
Friedreich's hereditary spinal ataxia
Friedreich's spinal ataxia
Hereditary spinal ataxia 2.Friedreich's disease
Holy thistle
Lady's thistle
Marie ataxia
Marie disease
Marie's ataxia
Marie's cerebellar ataxia
Marie's disease
Milk thistle
Nonne-Marie sydrome
Saint Mary's
Saint Mary's Band
St. Mary's Band
St. Mary's thistle

Traduction de «marie's ataxia » (Anglais → Français) :



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

hérédo-ataxie cérébelleuse de Pierre Marie


Friedreich's ataxia [ Friedreich's disease | Friedreich disease | Friedreich's hereditary spinal ataxia | Friedreich hereditary spinal ataxia | Friedreich familial ataxia | Friedreich's familial ataxia | Friedreich hereditary ataxia | Friedreich's hereditary ataxia | Friedreich spinocerebella ]

ataxie de Friedreich [ maladie de Friedreich | ataxie héréditaire ]


Saint Mary's [ Saint Mary's Band | St. Mary's Band ]

Saint Mary's [ bande Saint Mary's | bande St. Mary's ]




milk thistle | lady's thistle | St. Mary's thistle | holy thistle

chardon-Marie | chardon Notre-Dame | chardon argenté | artichaut sauvage | silybe de Marie | silybe


acromegaly | acromegalia | Marie's disease

acromégalie | maladie de Marie


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

hérédo-ataxie cérébelleuse


familiar ataxia | Friedreich's spinal ataxia | hereditary spinal ataxia 2.Friedreich's disease

ataxie de Friedreich | ataxie héréditaire | maladie de Friedreich | tabes héréditaire


Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo

ataxie spinocérébelleuse type 38


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