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Absence epilepsy
Benign myoclonic epilepsy in infancy
Childhood absence epilepsy
Clonic
Dravet syndrome
Dravet's syndrome
Epilepsy with myoclonic absences
Impulsive petit mal
Myoclonic
Myoclonic absence epilepsy
Myoclonic epilepsy
Myoclonic-astatic seizures
Neonatal convulsions
Nonspecific epileptic seizures atonic
Petit mal
Petit mal epilepsy
Pyknolepsy
SMEI
Severe myoclonic epilepsy of infancy
Tonic
Tonic-clonic

Vertaling van "epilepsy with myoclonic absences " (Engels → Nederlands) :

TERMINOLOGIE
Epilepsy with:myoclonic absences | myoclonic-astatic seizures | Infantile spasms Lennox-Gastaut syndrome Salaam attacks Symptomatic early myoclonic encephalopathy West's syndrome

epilepsie met | myoklonisch-astatische aanvallen | epilepsie met | myoklonische absences | infantiele spasmen | salaamkrampen | symptomatische myoklonische-encefalopathie, vroeg optredend | syndroom van Lennox-Gastaut | syndroom van West


Myoclonic absence epilepsy

myoklonische absence-epilepsie


Benign:myoclonic epilepsy in infancy | neonatal convulsions (familial) | Childhood absence epilepsy [pyknolepsy] Epilepsy with grand mal seizures on awakening Juvenile:absence epilepsy | myoclonic epilepsy [impulsive petit mal] | Nonspecific epileptic seizures:atonic | clonic | myoclonic | tonic | tonic-clonic

absence-epilepsie in kinderjaren [pyknolepsie] | benigne | infantiele myoklonische-epilepsie | benigne | neonatale convulsies (familiaal) | epilepsie met grandmalaanvallen bij ontwaken | juveniele | absence epilepsie | juveniele | myoklonische epilepsie [impulsieve petit mal] | niet-specifieke epileptische aanvallen | atonisch | niet-specifieke epileptische aanvallen | klonisch | niet-specifieke epileptische aanvallen | myoklonisch | niet-specifieke epileptische aanvallen | tonisch | niet-specifieke epileptische a ...[+++]




Dravet syndrome | Dravet's syndrome | severe myoclonic epilepsy of infancy | SMEI [Abbr.]

syndroom van Dravet | SMEI [Abbr.]


absence epilepsy | petit mal | petit mal epilepsy

absence epilepsie | epilepsie met absences


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

cryptogene epileptische spasmen met late aanvang


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

infantiele spasmen met late aanvang
IN-CONTEXT TRANSLATIONS
1 || KIEKIDS || 2011 || To develop an innovative, age-adapted, flexible and safe paediatric formulation of ethosuximide for the treatment of absence and of myoclonic epilepsies in children || NA

1 || KIEKIDS || 2011 || Ontwikkeling van een innovatieve, aan de leeftijd aangepaste, flexibele en veilige pediatrische formulering van ethosuximide voor de behandeling van het gebrek aan deze stof en van myoclonische epilepsie bij kinderen || N.v.t.




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Date index: 2021-06-17
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