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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
Labyrinthic ataxia
Labyrinthine ataxia
Locomotive disability
Locomotor ataxia
Locomotor disability
Locomotor impairment
Marie ataxia
Marie's ataxia
Marie's cerebellar ataxia
SCA1
SCA2
Spinocerebellar ataxia 1
Spinocerebellar ataxia 2
Spinocerebellar ataxia II
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 2
Tabes
Type 1 spinocerebellar ataxia
Vestibular ataxia

Traduction de «locomotor ataxia » (Anglais → Français) :

tabes | locomotor ataxia

tabès | ataxie locomotrice | ataxie locomotive




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 ]


vestibular ataxia [ labyrinthic ataxia | labyrinthine ataxia ]

ataxie labyrinthique [ ataxie vestibulaire ]


spinocerebellar ataxia 2 | SCA2 | spinocerebellar ataxia type 2 | spinocerebellar ataxia II

ataxie spinocérébelleuse 2 | SCA2


spinocerebellar ataxia 1 | SCA1 | type 1 spinocerebellar ataxia | spinocerebellar ataxia type 1

ataxie spinocérébelleuse 1 | ataxie spinocérébellaire 1 | ataxie spino-cérébelleuse de type I | ataxie spinocérébelleuse de type 1 | SCA 1


locomotive disability [ locomotor impairment | locomotor disability ]

handicap locomoteur


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

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


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

hérédo-ataxie cérébelleuse de Pierre Marie


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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