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Epi-Suisse
Epilepsy Association of Calgary
Epilepsy Manitoba
Manitoba Epilepsy Association
PAPA Calgary
Par Epi
Swiss Association of parents of children with epilepsy
Swiss Epilepsy Association
Western Canada League Against Epilepsy

Translation of "epilepsy association calgary " (English → French) :

Epilepsy Association of Calgary [ Western Canada League Against Epilepsy ]

Epilepsy Association of Calgary [ Western Canada League Against Epilepsy ]
Regional and Municipal Gov. Bodies and Committees | Nervous System
Organismes et comités de gouv. régionaux ou municipaux | Système nerveux


Professional Arts Publicists Association/Calgary and Southern Alberta [ PAPA Calgary | Performing Arts Publicists Association/Calgary and Southern Alberta ]

Professional Arts Publicists Association/Calgary and Southern Alberta [ PAPA Calgary | Performing Arts Publicists Association/Calgary and Southern Alberta ]
Private-Sector Bodies and Committees | Advertising
Organismes et comités du secteur privé | Publicité


Epilepsy Manitoba [ Manitoba Epilepsy Association ]

Epilepsy Manitoba [ Manitoba Epilepsy Association ]
Provincial Government Bodies and Committees (Canadian) | Nervous System
Organismes et comités de gouvernements provinciaux canadiens | Système nerveux


Swiss Epilepsy Association [ Epi-Suisse ]

Association suisse de l'épilepsie [ Epi-Suisse ]
Man & society
Organismes - mouvements (L'homme et la société) | Activités sociales (L'homme et la société)


A rare epilepsy syndrome characterized by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently

spasme cryptogénique à début tardif
SNOMEDCT-BE (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently / 778063003
SNOMEDCT-BE (disorder) / 778063003


A rare epilepsy syndrome characterised by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behaviour problems are frequentl

spasme infantile à début tardif
SNOMEDCT-BE (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently / 778063003
SNOMEDCT-BE (disorder) / 778063003


Rare childhood-onset epilepsy syndrome associated with infection and a biphasic clinical course. The initial symptom is a prolonged febrile seizure on day 1 (the first phase). Afterwards, patients have variable levels of consciousness from normal to

encéphalopathie aigüe du lobe frontal liée à la fièvre
SNOMEDCT-BE (the first phase). Afterwards, patients have variable levels of consciousness from normal to / 766044005
SNOMEDCT-BE (disorder) / 766044005


Swiss Association of parents of children with epilepsy | Par Epi

Association Suisse de Parents d'Enfants Epileptiques | Par Epi [ ASPEE ]
Medicine & biology | Man & society
Pathologie (Sciences médicales et biologiques) | Organismes - mouvements (L'homme et la société) | Activités sociales (L'homme et la société)


Swiss Association of parents of children with epilepsy; Par Epi

ASPEE | Association Suisse de Parents d'Enfants Épileptiques | Par Epi
IATE - Health
IATE - Health




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'epilepsy association calgary'

Date index:2022-02-03 -

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