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Athetosis
Brain MRI
Brain magnetic resonance imaging
Cerebral MRI
Cerebral dyspnea
Cerebral dyspnoea
Cerebral loiasis
Cerebral lymphoma
Cerebral magnetic resonance imaging
Cerebral palsy
Loiasis
Loiasis
MRI brain scan
Onchocerciasis
Phthiriasis
Primitive cerebral lymphoma

Traduction de «Cerebral loiasis » (Anglais → Néerlandais) :





Dermatitis of eyelid due to Demodex species (B88.0+) Parasitic infestation of eyelid in:leishmaniasis (B55.-+) | loiasis (B74.3+) | onchocerciasis (B73+) | phthiriasis (B85.3+)

dermatitis van ooglid door Demodex-species (B88.0) | parasitaire infestatie van ooglid bij | leishmaniasis (B55.-) | parasitaire infestatie van ooglid bij | loiasis (B74.3) | parasitaire infestatie van ooglid bij | onchocerciasis (B73) | parasitaire infestatie van ooglid bij | phthiriasis (B85.3)


brain magnetic resonance imaging | brain MRI | cerebral magnetic resonance imaging | cerebral MRI | MRI brain scan

kernspintomografie van de schedel | KST van de schedel | NMR van de schedel




cerebral lymphoma | primitive cerebral lymphoma

primair cerebraal lymfoom


Definition: Includes cases with a history of hypertension and foci of ischaemic destruction in the deep white matter of the cerebral hemispheres. The cerebral cortex is usually preserved and this contrasts with the clinical picture which may closely resemble that of dementia in Alzheimer's disease.

Omschrijving: Omvat gevallen met een voorgeschiedenis van hypertensie en foci van ischemische destructie in de diepgelegen witte stof van de cerebrale hemisferen. De cerebrale cortex is doorgaans gespaard gebleven en dit contrasteert met het klinische beeld dat sterk kan lijken op dat van dementie bij de ziekte van Alzheimer.


Grange syndrome has characteristics of stenosis or occlusion of multiple arteries (including the renal, cerebral and abdominal vessels), hypertension, brachysyndactyly, syndactyly, increased bone fragility, and learning difficulties or borderline int

syndroom van progressieve arteriële occlusieve ziekte, hypertensie, hartdefect, botfragiliteit en brachysyndactylie


Spinocerebellar ataxia type 31 (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense,

spinocerebellaire ataxie type 31


athetosis | cerebral palsy

athetose | onwillekeurige bewegingen van vingers en tenen




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'Cerebral loiasis' ->

Date index: 2023-04-08
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