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Medieval history
Middle Age
Middle Ages
Middle age temptations
Middle ages
Middle-age temptation
Middle-aged
Middle-aged old
Middle-aged person

Translation of "middle-age temptation " (English → French) :

middle age temptations [ middle-age temptation ]

démon de midi
Translation | Language Problems
Traduction | Problèmes de langue


medieval history [ Middle Ages | middle ages(UNBIS) ]

histoire médiévale [ Moyen Âge ]
36 SCIENCE | MT 3611 humanities | BT1 history | BT2 social sciences | RT heraldry [2831]
36 SCIENCES | MT 3611 sciences humaines | BT1 histoire | BT2 sciences sociales | RT héraldique [2831]


middle-aged [ middle-aged old ]

d'âge moyen [ moyennement âgé ]
Anthropology
Anthropologie


Middle Ages [ Middle Age ]

Moyen Âge [ Moyen-Âge ]
History (General)
Histoire (Généralités)


Middle Ages

Moyen-Âge | MA [Abbr.]
IATE - Humanities
IATE - Humanities


middle-aged person

demi vieux
IATE - SOCIAL QUESTIONS
IATE - SOCIAL QUESTIONS


Definition: A progressive dementia with extensive neurological signs, due to specific neuropathological changes that are presumed to be caused by a transmissible agent. Onset is usually in middle or later life, but may be at any adult age. The course is subacute, leading to death within one to two years.

Définition: Démence évoluant progressivement, comportant des signes neurologiques étendus, due à des altérations neuropathologiques spécifiques que l'on suppose provoquées par un agent transmissible. Elle débute habituellement à l'âge mûr ou plus tard, mais peut débuter chez l'adulte à n'importe quel âge. Son évolution est subaiguë, aboutissant à la mort en un à deux ans.
WORLD HEALTH ORGANIZATION ICD-10: F02.1*
WORLD HEALTH ORGANIZATION ICD-10: F02.1*


Definition: A progressive dementia, commencing in middle age, characterized by early, slowly progressing changes of character and social deterioration, followed by impairment of intellect, memory, and language functions, with apathy, euphoria and, occasionally, extrapyramidal phenomena.

Définition: Démence évoluant progressivement, débutant à l'âge mûr, caractérisée par des modifications précoces, lentement progressives, du caractère et par une détérioration sociale, aboutissant à une déficience des fonctions intellectuelles, de la mémoire et du langage, accompagnées d'une apathie, d'une euphorie et, plus rarement, de symptômes extra-pyramidaux.
WORLD HEALTH ORGANIZATION ICD-10: F02.0*
WORLD HEALTH ORGANIZATION ICD-10: F02.0*


A very rare progressive and untreatable disease with manifestations of ataxia with sensory neuropathy. Prevalence is unknown, typically starts in middle-aged adults and presents with cerebellar ataxia, pyramidal signs, and peripheral sensory loss. Th

ataxie spinocérébelleuse type 4
SNOMEDCT-BE (disorder) / 715755008
SNOMEDCT-BE (disorder) / 715755008


An extremely rare glial neoplasm occurring in the region of the anterior third ventricle or hypothalamus, which is non-infiltrative and well-circumscribed and presents most frequently in middle-aged women with symptoms of memory loss and headaches an

gliome chordoïde
SNOMEDCT-BE (disorder) / 715900001
SNOMEDCT-BE (disorder) / 715900001




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Date index:2022-11-26 -

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