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Agent de l'encéphalopathie spongiforme subaiguë
Alpers
Encéphalopathie nécrosante aigüe familiale
Encéphalopathie nécrosante subaiguë
Encéphalopathie spongieuse subaiguë
Leigh
Myélite nécrosante subaiguë
Myélite subaigüe nécrosante

Translation of "Encéphalopathie nécrosante subaiguë " (French → English) :

TERMINOLOGY
see also In-Context Translations below
Corps de Lewy (maladie à) (démence à) Dégénérescence de la substance grise [Alpers] Encéphalopathie nécrosante subaiguë [Leigh]

Grey-matter degeneration [Alpers] Lewy body(ies)(dementia)(disease) Subacute necrotizing encephalopathy [Leigh]
WORLD HEALTH ORGANIZATION ICD-10: G31.8
WORLD HEALTH ORGANIZATION ICD-10: G31.8


Myélite nécrosante subaiguë

Subacute necrotizing myelitis
WORLD HEALTH ORGANIZATION ICD-10: G37.4
WORLD HEALTH ORGANIZATION ICD-10: G37.4


encéphalopathie nécrosante aigüe familiale

A potentially fatal neurological disease with characteristics of neuropathological lesions principally involving the brainstem, thalamus and putamen. It has been described in 11 members of one family. Onset occurs during early childhood, typically a
SNOMEDCT-BE (disorder) / 723359002
SNOMEDCT-BE (disorder) / 723359002


agent de l'encéphalopathie spongiforme subaiguë

Jakob-Creutzfeld agent
SNOMEDCT-CA (organisme) / 88520007
SNOMEDCT-CA (organisme) / 88520007


démence causée par l'encéphalopathie spongiforme subaiguë

Dementia due to Creutzfeldt Jakob disease
SNOMEDCT-CA (trouble) / 429458009
SNOMEDCT-CA (trouble) / 429458009


dégénérescence cérébrale causée par l'encéphalopathie spongiforme subaiguë

Cerebral degeneration due to Creutzfeldt-Jakob disease
SNOMEDCT-CA (trouble) / 192818008
SNOMEDCT-CA (trouble) / 192818008


Encéphalopathie spongieuse subaiguë

Subacute spongiform encephalopathy
WORLD HEALTH ORGANIZATION ICD-10: A81.0
WORLD HEALTH ORGANIZATION ICD-10: A81.0


myélite subaigüe nécrosante

Subacute necrotising myelitis
SNOMEDCT-BE (disorder) / 230379007
SNOMEDCT-BE (disorder) / 230379007
IN-CONTEXT TRANSLATIONS
Il a été établi que la prise de suppléments de thiamine constitue un moyen efficace de traiter les carences en thiamine, les troubles métaboliques associés à des maladies héréditaires (par ex. l'encéphalopathie nécrosante subaiguë [ou syndrome de Leigh], la leucinose [ou maladie du sirop d’érable] et l'acidose lactique) et le syndrome de Wernicke-Korsakoff.

Thiamine supplementation has been shown to be effective in treating thiamine deficiency, metabolic disorders associated with genetic disease (e.g., subacute necrotizing encephalopathy also known as Leigh's disease, maple syrup urine disease, and lactic acidosis), and Wernicke-Korsakoff syndrome (WKS).




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Encéphalopathie nécrosante subaiguë

Date index:2022-07-27 -

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