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Apply support for spinal adjustment
Apply supports for spinal adjustment
Apply supports for spinal adjustments
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's ataxia
Marie's cerebellar ataxia
Myoclonus
Retained tendon reflexes
Spinal ataxia
Use supports for spinal adjustments

Vertaling van "Spinal ataxia " (Engels → Nederlands) :



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


apply support for spinal adjustment | apply supports for spinal adjustments | apply supports for spinal adjustment | use supports for spinal adjustments

ondersteuningsmiddelen aanbrengen voor de correctie van de ruggengraat


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

cerebellaire heredo-ataxie


This disease has characteristics of progressive cerebellar ataxia with pyramidal and spinal cord dysfunction, associated with distinctive MRI anomalies and increased lactate in the abnormal white matter. Onset occurs in early childhood. Epilepsy and

leuko-encefalopathie met betrokkenheid van hersenstam en ruggenmerg, hoog lactaatgehalte-syndroom


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


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

spinocerebellaire ataxie type 26


Acute infarction of spinal cord (embolic)(nonembolic) Arterial thrombosis of spinal cord Haematomyelia Nonpyogenic intraspinal phlebitis and thrombophlebitis Oedema of spinal cord Subacute necrotic myelopathy

acute infarcering van ruggenmerg (embolisch)(niet-embolisch) | arteriële trombose van ruggenmerg | hematomyelie | niet-pyogene intraspinale-flebitis en -tromboflebitis | ruggenmergoedeem | subacute necrotische-myelopathie


hydromeningocele (spinal) meningocele (spinal) meningomyelocele myelocele myelomeningocele rachischisis spina bifida (aperta)(cystica) syringomyelocele

hydromeningokèle (spinaal) | meningokèle (spinaal) | meningomyelokèle | myelokèle | myelomeningokèle | rachischisis | spina bifida (aperta)(cystica) | syringomyelokèle




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'Spinal ataxia' ->

Date index: 2022-03-11
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