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Dementia in Huntington's chorea
Slow onset emergency
Slow onset event

Vertaling van "slow onset emergency " (Engels → Nederlands) :

slow onset emergency | slow onset event
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
traag op gang komend verschijnsel
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Definition: A dementia occurring as part of a widespread degeneration of the brain. The disorder is transmitted by a single autosomal dominant gene. Symptoms typically emerge in the third and fourth decade. Progression is slow, leading to death usually within 10 to 15 years. | Dementia in Huntington's chorea
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Omschrijving: Een dementie die optreedt als onderdeel van een uitgebreide degeneratie van de hersenen. De stoornis vererft via een enkel autosomaal dominant gen. Typerend is het manifest worden van de symptomen in de derde en vierde decade. Progressie is langzaam, gewoonlijk in 10 tot 15 jaar tot de dood leidend. | Neventerm: | dementie bij chorea van Huntington
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
A form of Parkinson disease with age of onset between 21 and 45 years, rigidity, painful cramps followed by tremor, bradykinesia, dystonia, gait complaints, falls and other non-motor symptoms. A slow disease progression and a more pronounced response
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
ziekte van Parkinson met aanvang op jonge leeftijd
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Disease with characteristics of early-onset of cerebellar signs with eye movement abnormalities and a very slow disease progression.Three families have been reported to date. Clinical manifestations include cerebellar signs (ataxia, dysarthria, and i
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
spinocerebellaire ataxie type 5
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
An early-onset chorioretinal dystrophy with characteristics of large atrophic macular and nasal retinal lesions, nystagmus, myopia, poor vision and slow disease progression. It has been described in two large families. Transmission is autosomal domin
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
progressieve bifocale chorioretinale atrofie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : dementia in huntington's chorea     slow onset emergency     slow onset event     


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Date index: 2022-10-17
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