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Active disease
Aran-Duchenne disease
Chronic progressive hereditary chorea
Control fish diseases
Controlling disease in fish
Controlling fish diseases
Cruveilhier disease
Diagnose a heart condition
Diagnose heart conditions
HD
Huntington chorea
Huntington disease
Huntington's chorea
Huntington's disease
Identify cardiovascular diseases
Identify heart diseases
Identify progression of disease
Identify progression of diseases
Identifying fish diseases
PMA
Progressive disease
Progressive muscular atrophy
Progressive spinal muscular atrophy
Recognise changing symptoms of a disease
Recognise progression of disease
SMA
SPMA
Spinal muscular atrophy
Spinal progressive muscular atrophy

Vertaling van "identify progression disease " (Engels → Nederlands) :

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


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