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Benign myoclonic epilepsy in infancy
Childhood absence epilepsy
Clonic
Dravet syndrome
Dravet's syndrome
Epilepsy with myoclonic absences
Impulsive petit mal
Myoclonic
Myoclonic epilepsy
Myoclonic epilepsy in non-progressive encephalopathy
Myoclonic-astatic seizures
Neonatal convulsions
Nonspecific epileptic seizures atonic
Progressive myoclonic epilepsy
Progressive myoclonic epilepsy 1B
Pyknolepsy
SMEI
Severe myoclonic epilepsy of infancy
Tonic
Tonic-clonic

Vertaling van "Progressive myoclonic epilepsy " (Engels → Nederlands) :

Progressive myoclonic epilepsy
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
progressieve myoklonische epilepsie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Progressive myoclonic epilepsy 1B
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progressieve myoclonusepilepsie met ataxie
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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
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 aanvallen | tonisch-klonisch
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Myoclonic epilepsy in non-progressive encephalopathy
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myoclonische epilepsie bij niet-progressieve encefalopathieën
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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Dravet syndrome | Dravet's syndrome | severe myoclonic epilepsy of infancy | SMEI [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
syndroom van Dravet | SMEI [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
myoclonic epilepsy
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
myoclonische epilepsie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Epilepsy with:myoclonic absences | myoclonic-astatic seizures | Infantile spasms Lennox-Gastaut syndrome Salaam attacks Symptomatic early myoclonic encephalopathy West's syndrome
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
epilepsie met | myoklonisch-astatische aanvallen | epilepsie met | myoklonische absences | infantiele spasmen | salaamkrampen | symptomatische myoklonische-encefalopathie, vroeg optredend | syndroom van Lennox-Gastaut | syndroom van West
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Definition: The schizophrenic disorders are characterized in general by fundamental and characteristic distortions of thinking and perception, and affects that are inappropriate or blunted. Clear consciousness and intellectual capacity are usually maintained although certain cognitive deficits may evolve in the course of time. The most important psychopathological phenomena include thought echo; thought insertion or withdrawal; thought broadcasting; delusional perception and delusions of control; influence or passivity; hallucinatory voices commenting or discussing the patient in the third person; thought disorders and negative symptoms. The course of schizophrenic disorders can be either continuous, or episodic with ...[+++]
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Omschrijving: De schizofrene stoornissen worden in het algemeen gekarakteriseerd door fundamentele en kenmerkende verstoringen van denken en waarneming en door een inadequaat of vlak affect. Helder bewustzijn en intellectueel vermogen zijn doorgaans behouden, zij het dat bepaalde cognitieve tekortkomingen zich in de loop des tijds kunnen ontwikkelen. De belangrijkste psychopathologische verschijnselen omvatten 'Gedankenlautwerden'; gedachteninbrenging of -onttrekking; gedachtenuitzending; waanwaarneming en wanen omtrent het onder controle van derden staan; macht of passiviteit; gehallucineerde stemmen die de patiënt bekritiseren of over deze praten in de derde persoon; denkstoornissen en negatieve symptomen. | Het beloop van schizofre ...[+++]
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : benign myoclonic epilepsy in infancy     childhood absence epilepsy     dravet syndrome     dravet's syndrome     epilepsy with myoclonic absences     myoclonic epilepsy in non-progressive encephalopathy     nonspecific epileptic seizures atonic     progressive myoclonic epilepsy     progressive myoclonic epilepsy 1b     clonic     impulsive petit mal     myoclonic     myoclonic epilepsy     myoclonic-astatic seizures     neonatal convulsions     pyknolepsy     severe myoclonic epilepsy of infancy     tonic-clonic     Progressive myoclonic epilepsy     


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Date index: 2023-05-24
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