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Asthenic bulbar paralysis
Aujeszky's disease
Bulbar paralysis
Distal
Duchenne's paralysis
Duchenne's syndrome
Fazio-Londe
Infectious bulbar paralysis
Kugelberg-Welander
Labioglossolaryngeal paralysis
Mad itch
Primary
Progressive bulbar palsy
Progressive bulbar palsy of childhood
Progressive bulbar paralysis
Pseudorabies
Scapuloperoneal form
Spinal muscular atrophy
Spinal muscular atrophy adult form

Vertaling van "progressive bulbar paralysis " (Engels → Nederlands) :

bulbar paralysis | Duchenne's paralysis | Duchenne's syndrome | labioglossolaryngeal paralysis | progressive bulbar palsy | progressive bulbar paralysis

bulbaire paralyse | labioglossolaryngeole verlamming | syndroom van Duchenne


asthenic bulbar paralysis

asthenische bulbaire verlamming | myasthenia gravis pseudoparalytica


Aujeszky's disease | infectious bulbar paralysis | mad itch | pseudorabies

pseudorabiës | ziekte van Aujeszky


Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy:adult form | childhood form, type II | distal | juvenile form, type III [Kugelberg-Welander] | scapuloperoneal form

progressieve bulbairparalyse in kinderjaren [Fazio-Londe] | spinale spieratrofie | distaal | spinale spieratrofie | juveniele vorm, type III [Kugelberg-Welander] | spinale spieratrofie | scapuloperoneale vorm | spinale spieratrofie | van kinderleeftijd, type II | spinale spieratrofie | volwassen vorm


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


A rare genetic disorder of thiamine metabolism and transport with characteristics of the childhood-onset of recurrent episodes of flaccid paralysis and encephalopathy, associated with bilateral striatal necrosis and chronic progressive axonal polyneu

progressieve polyneuropathie met bilaterale striatale necrose




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Date index: 2021-10-17
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