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Congenital cerebellar ataxia
Disease Charcot-Marie-Tooth
Déjerine-Sottas
Early-onset cerebellar ataxia with essential tremor
Familiar ataxia
Friedreich's spinal ataxia
Hereditary spinal ataxia 2.Friedreich's disease
Hunt's ataxia
Marie ataxia
Marie cerebellar ataxia
Marie disease
Marie's ataxia
Marie's cerebellar ataxia
Marie's disease
Marie-Bamberger disease Pachydermoperiostosis
Myoclonus
Nonne-Marie sydrome
Retained tendon reflexes

Vertaling van "marie's ataxia " (Engels → Nederlands) :

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

cerebellaire heredo-ataxie


Marie cerebellar ataxia

hereditaire cerebellaire ataxie van Pierre Marie


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

erfelijke cerebellaire ataxie


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

ataxia hereditaria | ataxie van Friedreich | spinale heredo-ataxie van Friedreich | tabes van Friedreich


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

spinocerebellaire ataxie type 38


Early-onset cerebellar ataxia with:essential tremor | myoclonus [Hunt's ataxia] | retained tendon reflexes | Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia

Friedreich-ataxie (autosomaal recessief) | vroeg optredende cerebellaire ataxie met | behouden peesreflexen | vroeg optredende cerebellaire ataxie met | essentiële tremor | vroeg optredende cerebellaire ataxie met | myoclonus [Hunts ataxie] | recessieve spinocerebellaire ataxie, X-gebonden


Charcot-Marie-Tooth disease, type 4B2 (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso

ziekte van Charcot-Marie-Tooth type 4B2


Marie-Bamberger disease Pachydermoperiostosis

pachydermoperiostose | ziekte van Marie-Bamberger


Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome

hereditaire motorische- en sensorische-neuropathie, type I-IV | infantiele hypertrofische-neuropathie | peroneale spieratrofie (axonaal type)(hypertrofisch type) | syndroom van Roussy-Lévy | ziekte van | Charcot-Marie-Tooth | ziekte van | Déjerine-Sottas




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Date index: 2022-09-22
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