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Ataxie spino-cérébelleuse de type I
Ataxie spinocérébellaire 1
Ataxie spinocérébelleuse 1
Ataxie spinocérébelleuse de type 1
Ataxie spinocérébelleuse type 36
Ataxie spinocérébelleuse type 37
Ataxie spinocérébelleuse type 40
SCA 1

Traduction de «Ataxie spinocérébelleuse type 37 » (Français → Anglais) :

ataxie spinocérébelleuse type 37

Disease with characteristics of cerebellar syndrome along with altered vertical eye movements. Reported in nine members of Spanish kindred to date. Disease onset occurs in adulthood (from the ages of 38-64). Clinical manifestations are slowly progres


ataxie spinocérébelleuse 1 | ataxie spinocérébellaire 1 | ataxie spino-cérébelleuse de type I | ataxie spinocérébelleuse de type 1 | SCA 1

spinocerebellar ataxia 1 | SCA1 | type 1 spinocerebellar ataxia | spinocerebellar ataxia type 1


ataxie spinocérébelleuse type 36

Costa de Morte ataxia


ataxie spinocérébelleuse type 40

A very rare disease with characteristics of adult-onset unsteady gait and dysarthria, followed by wide-based gait, gait ataxia, ocular dysmetria, intention tremor, scanning speech, hyperreflexia and dysdiadochokinesis.




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Ataxie spinocérébelleuse type 37 ->

Date index: 2021-10-13
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