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Batten disease
Bulbar motor neuron disease
Central motor neuron
Disease Charcot-Marie-Tooth
Déjerine-Sottas
Motor neuron disease
NCL
Neuronal ceroid lipofuscinosis
Peripheral motor neuron
Primary
Progressive bulbar palsy
Spinal muscular atrophy

Traduction de «motor neuron disease » (Anglais → Néerlandais) :

Bulbar motor neuron disease

amyotrofe laterale sclerose


Familial motor neuron disease Lateral sclerosis:amyotrophic | primary | Progressive:bulbar palsy | spinal muscular atrophy

familiale ziekte van motorische neuronen | laterale sclerose | amyotrofe | laterale sclerose | primaire | progressieve | bulbairparalyse | progressieve | spinale spieratrofie






A rare genetic motor neuron disease with characteristics of progressive early respiratory failure associated with diaphragm paralysis, distal muscular weakness, joint contractures, and axial hypotonia with preserved antigravity limb movements. The ph

spinale spieratrofie met respiratoire insufficiëntie type 2






Batten disease | neuronal ceroid lipofuscinosis | NCL [Abbr.]

amaurotisch idiotisme


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: 2024-07-01
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