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AKEL
Acrodermatitis chronica atrophicans
Amyotrofe
Bulbairparalyse
Erythromelia
Erythromelie
Familiale ziekte van motorische neuronen
Glomerulaire aandoening
Glomerulonefritis
Laterale sclerose
Nefritis
PD
Primaire
Progressieve
Progressieve Arbeiderspartij
Progressieve Partij van de Werkende Klasse
Progressieve atrofiërendedermatitis
Progressieve democraten
Progressieve multifocale leuko-encefalopathie
Snel progressieve
Spinale spieratrofie
Ziekte van Pick

Vertaling van "Progressieve atrofiërendedermatitis " (Nederlands → Engels) :

acrodermatitis chronica atrophicans | erythromelia | erythromelie | progressieve atrofiërendedermatitis | ziekte van Pick

erythromelia Pick


snel progressieve | glomerulaire aandoening | snel progressieve | glomerulonefritis | snel progressieve | nefritis

rapidly progressive:glomerular disease | glomerulonephritis | nephritis


Progressieve Arbeiderspartij | Progressieve Partij van de Werkende Klasse | AKEL [Abbr.]

Communist Party | Progressive Party of the Working People | AKEL [Abbr.]


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

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


Progressieve democraten | PD [Abbr.]

Progressive Democrats | PD [Abbr.] | PDs [Abbr.]


progressieve neurodegeneratie met vroege aanvang, blindheid, ataxie, spasticiteit

A genetic neurodegenerative disease with normal early development followed by childhood onset optic atrophy with progressive vision loss and eventually blindness, followed by progressive neurological decline that typically includes cerebellar ataxia,


autosomaal dominante progressieve nefropathie met hypertensie

Autosomal dominant progressive nephropathy with hypertension


progressieve multifocale leuko-encefalopathie

Progressive multifocal leukoencephalopathy


chronische progressieve externe oftalmoplegie met mitochondriale myopathie met aanvang op volwassen leeftijd

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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Date index: 2022-05-12
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