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Briquet ataxia
Briquet machine operator
Briquet's ataxia
Briquette maker
Briquetter operator
Briquetting machine operator
Canadian Association of Familial Ataxias
Canadian Association of Friedrich's 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
Marie ataxia
Marie's ataxia
Marie's cerebellar ataxia

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



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 ]


Canadian Association of Familial Ataxias [ Canadian Association of Friedrich's Ataxia ]

Association Canadienne des Ataxies Familiales [ ACAF | Association canadienne de l'Ataxie de Friedreich ]






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


briquette maker | briquetter operator | briquet machine operator | briquetting machine operator

opérateur sur machine à briqueter | opérateur sur machine à briqueter/opératrice sur machine à briqueter | opératrice sur machine à briqueter


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


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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