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Nerval impairment of motion
Nerval incoordination of movements
Nerval motor disturbance
Psychogenic impairment of motion
Psychogenic incoordination of movements
Psychogenic motor disturbance
Pyramidal incoordination of movements
Pyramidal motor disturbance

Vertaling van "pyramidal incoordination movements " (Engels → Frans) :

pyramidal incoordination of movements | pyramidal motor disturbance

syndrome pyramidal | trouble moteur pyramidal


nerval impairment of motion | nerval incoordination of movements | nerval motor disturbance

trouble moteur neurogène


psychogenic impairment of motion | psychogenic incoordination of movements | psychogenic motor disturbance

trouble moteur psychogène


A rare neurologic disease characterized by global developmental delay, intellectual disability, multiple ischemic lesions on brain MRI, behavioral abnormalities, dystonia, choreic movements and pyramidal syndrome, facial dysmorphism (hypertelorism, a

syndrome autosomique récessif de leucoencéphalopathie-infarctus cérébraux-rétinite pigmentaire


A rare hereditary ataxia with characteristics of delayed early motor development, severe neonatal hypotonia, non-progressive ataxia and slow eye movements, presenting normal cognitive abilities and absence of pyramidal signs. Frequently patients also

ataxie cérébelleuse liée à l'X non progressive


Disease with characteristics of early-onset cerebellar signs, eye movement abnormalities and pyramidal signs. Fifty-one clinically affected members from four families (of British, Pakistani, German and French descent) have been reported to date. The

ataxie spinocérébelleuse type 11




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Date index: 2024-01-18
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