Traduction de «Identify progression diseases » (Anglais → Néerlandais) :

recognise changing symptoms of a disease | recognise progression of disease | identify progression of disease | identify progression of diseases
voortgang van ziekte identificeren | voortgang van ziekte vaststellen

diagnose a heart condition | identify cardiovascular diseases | diagnose heart conditions | identify heart diseases
hartaandoeningen vaststellen

controlling disease in fish | controlling fish diseases | control fish diseases | identifying fish diseases
visziekten beheersen

active disease | progressive disease
evolutieve ziekte | progressieve ziekte

An inherited epileptic syndrome characterized by cortical hand tremors, myoclonic jerks and occasional generalized or focal seizures with a non-progressive or very slowly progressive disease course, and no signs of early dementia or cerebellar ataxia
goedaardige familiale myoclonische epilepsie, volwassen vorm

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

Spinocerebellar ataxia type 29 (SCA29) is a rare disease with main features of very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability. SCA29 presents at birth, or shortly, after with manife
congenitale niet-progressieve spinocerebellaire ataxie

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
spinocerebellaire ataxie type 38

chronic progressive hereditary chorea | Huntington chorea | Huntington disease | Huntington's chorea | Huntington's disease | HD [Abbr.]
chorea van Huntington | ziekte van Huntington

Definition: Dementia in Alzheimer's disease with onset after the age of 65, usually in the late 70s or thereafter, with a slow progression, and with memory impairment as the principal feature. | Alzheimer's disease, type 1 Primary degenerative dementia of the Alzheimer's type, senile onset Senile dementia, Alzheimer's type
Omschrijving: Dementie bij de ziekte van Alzheimer die optreedt na het 65e jaar, doorgaans na het 75e jaar of nog later, met een langzame progressie en met geheugenzwakte als belangrijkste kenmerk. | Neventerm: | primair degeneratieve dementie van het Alzheimer-type met aanvang in het senium | seniele dementie, Alzheimer-type | ziekte van Alzheimer, type 1