Pages that link to "Property:P68"
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The following pages link to Canonical URI (P68):
Displaying 50 items.
- Epilepsy due to tumours of the nervous system (Q41190) (← links)
- Epilepsy due to prenatal or perinatal brain insults (Q41191) (← links)
- Epilepsy with mesial temporal sclerosis (Q41192) (← links)
- Epilepsy due to abnormalities of brain development (Q41193) (← links)
- Epilepsy due to genetic syndromes with widespread or progressive effects (Q41194) (← links)
- Epilepsy due to prenatal or perinatal vascular insults (Q41195) (← links)
- Epilepsy due to cerebrovascular disorders (Q41196) (← links)
- Epilepsy due to injuries to the head (Q41197) (← links)
- Epilepsy due to central nervous system infections or infestations (Q41198) (← links)
- Epilepsy due to immune disorders (Q41199) (← links)
- Epilepsy due to multiple sclerosis or other demyelinating disorders (Q41200) (← links)
- Epilepsy due to dementias (Q41201) (← links)
- Epilepsy due to structural or metabolic conditions or diseases (Q41202) (← links)
- Myoclonic absences or absences with myoclonias (Q41203) (← links)
- Pyridoxal dependent epilepsy (Q41204) (← links)
- Genetic epileptic syndromes with childhood onset (Q41205) (← links)
- Progressive myoclonic epilepsy (Q41206) (← links)
- Epilepsy of infancy with migrating focal seizures (Q41207) (← links)
- Dravet syndrome (Q41208) (← links)
- Genetic epileptic syndromes with variable age of onset (Q41209) (← links)
- Benign adult familial myoclonus epilepsy (Q41210) (← links)
- Epilepsy with myoclonic-astatic seizures (Q41211) (← links)
- Juvenile myoclonic epilepsy (Q41212) (← links)
- Genetic epileptic syndromes with onset in infancy (Q41213) (← links)
- Juvenile absence epilepsy (Q41214) (← links)
- Genetic epileptic syndrome with adolescent or adult onset (Q41215) (← links)
- Benign childhood epilepsy with centro-temporal spikes (Q41216) (← links)
- Genetic epileptic syndromes with neonatal onset (Q41217) (← links)
- Reflex epilepsies (Q41218) (← links)
- Benign familial infantile epilepsy (Q41219) (← links)
- Genetic or presumed genetic syndromes primarily expressed as epilepsy (Q41220) (← links)
- Epileptic encephalopathies (Q41221) (← links)
- Infantile spasms (Q41222) (← links)
- Lennox-Gastaut syndrome (Q41223) (← links)
- Generalised tonic-clonic seizure (Q41224) (← links)
- Single unprovoked seizure (Q41225) (← links)
- Childhood absence epilepsy (Q41226) (← links)
- Convulsive status epilepticus (Q41227) (← links)
- Status epilepticus (Q41228) (← links)
- Non-convulsive status epilepticus (Q41229) (← links)
- Absence status epilepticus (Q41230) (← links)
- Acute repetitive seizures (Q41231) (← links)
- Migraine (Q41232) (← links)
- Chronic migraine (Q41233) (← links)
- Cyclic vomiting syndrome (Q41234) (← links)
- Migraine without aura (Q41235) (← links)
- Hemiplegic migraine (Q41236) (← links)
- Migraine with aura (Q41237) (← links)
- Status migrainosus (Q41238) (← links)
- Complications related to migraine (Q41239) (← links)
