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Acrocyanosis Acroparaesthesia simple
Blood flow-related
Early-onset cerebellar ataxia with essential tremor
Erythrocyanosis Erythromelalgia
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
Nothnagel's type
Retained tendon reflexes
Schultze's type
Vasomotor
Vasomotor and allergic rhinitis
Vasomotor ataxia

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



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

cerebellaire heredo-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


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


A rare hereditary ataxia with characteristics of progressive cerebellar ataxia associated with disruption of visual fixation by saccadic intrusions. It presents with progressive gait, trunk and limb ataxia with pyramidal tract signs (increased tendon

autosomaal recessieve cerebellaire ataxie, korte oogbeweging-intrusie


vasomotor | blood flow-related

vasomotorisch | van invloed op de omvang van bloedvaten


Vasomotor and allergic rhinitis

vasomotore en allergische rinitis


Acrocyanosis Acroparaesthesia:simple [Schultze's type] | vasomotor [Nothnagel's type] | Erythrocyanosis Erythromelalgia

acrocyanose | acroparesthesie | eenvoudig [type Schultze] | acroparesthesie | vasomotoor [type Nothnagel] | erytrocyanose | erytromelalgie




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'Vasomotor ataxia' ->

Date index: 2024-08-07
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