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.

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

ataxie spinocérébelleuse type 40

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

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

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ataxie spinocérébelleuse type 38

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A rare mitochondrial disease with characteristics of adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, manifestations of spinocerebellar ataxia (e.g. impaired gait, dysarthria) and mild motor peripheral neuro

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ophtalmoplégie externe progressive chronique de l'adulte avec myopathie mitochondriale

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

analysing animal locomotion and gait | animal locomotion analysing | analyse animal locomotion | analysing animal locomotion

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

analyser la locomotion d’un animal

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]

Abnormalities of gait and mobility

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Anomalies de la démarche et de la motilité