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Aran-Duchenne disease
Cruveilhier disease
Distal
Fazio-Londe
ISA
Infantile spinal amyotrophy
Kugelberg-Welander
PMA
Primary
Progressive bulbar palsy
Progressive bulbar palsy of childhood
Progressive muscular atrophy
Progressive spinal amyotrophy
Progressive spinal muscular atrophy
SMA
SPMA
Scapuloperoneal form
Spinal muscular atrophy
Spinal muscular atrophy adult form
Spinal progressive muscular atrophy

Vertaling van "Progressive spinal amyotrophy " (Engels → Frans) :

progressive spinal amyotrophy

amyotrophie nucléaire progressive


Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]

amyotrophie d'Aran-Duchenne | amyotrophie spinale progressive | atrophie de Cruveilhier | atrophie musculaire progressive d'Aran | maladie d'Aran-Duchenne


infantile spinal amyotrophy | ISA [Abbr.]

amyotrophie spinale infantile | ASI [Abbr.]


progressive spinal muscular atrophy

atrophie musculaire progressive


A genetic non-syndromic congenital malformation of the neurenteric canal, spinal cord and column characterized by progressive neurologic deterioration (pain, sensorimotor deficits, abnormal gait, decreased tone or abnormal reflexes), musculoskeletal

syndrome de la moelle attachée primaire


This disease has characteristics of progressive cerebellar ataxia with pyramidal and spinal cord dysfunction, associated with distinctive MRI anomalies and increased lactate in the abnormal white matter. Onset occurs in early childhood. Epilepsy and

syndrome de leucoencéphalopathie avec atteinte du tronc cérébral et de la moelle épinière-élévation des lactates


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

Amyotrophie spinale progressive Dégénérescence familiale du neurone moteur Paralysie bulbaire progressive Sclérose latérale:amyotrophique | primitive


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

Amyotrophie spinale (de):adulte | distale | enfant, type II | forme juvénile, type III [Kugelberg-Welander] | forme scapulo-péronière | Paralysie bulbaire progressive de l'enfant [Fazio-Londe]


Progressive non-infectious anterior vertebral fusion (PAVF) is an early childhood spinal disorder with characteristics of the gradual onset of thoracic and/or lumbar spine ankylosis often in conjunction with kyphosis with distinctive radiological fea

syndrome de Copenhague




datacenter (1): www.wordscope.be (v4.0.br)

'Progressive spinal amyotrophy' ->

Date index: 2021-05-19
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