Pages that link to "Property:P78"
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The following pages link to Knowledge Architect (P78):
Displaying 50 items.
- Demyelination due to mitochondrial disease (Q41152) (← links)
- White matter disorder due to CADASIL (Q41154) (← links)
- Neuromyelitis optica myelin oligodendrocyte glycoprotein antibody-positive (Q41156) (← links)
- White matter disorders due to nutritional deficiency (Q41158) (← links)
- Demyelination due to sarcoidosis (Q41160) (← links)
- White matter disorders due to vascular abnormality or ischemia (Q41162) (← links)
- Leukodystrophies (Q41164) (← links)
- Demyelination due to Behcet disease (Q41166) (← links)
- White matter disorder due to vitamin B12 deficiency (Q41168) (← links)
- Alexander disease (Q41170) (← links)
- Adrenoleukodystrophy (Q41172) (← links)
- Krabbe disease (Q41174) (← links)
- White matter disorders due to certain specified systemic disease (Q41176) (← links)
- Neuromyelitis optica aquaporin-4 antibody negative (Q41177) (← links)
- Neuromyelitis optica (Q41178) (← links)
- Single transverse myelitis aquaporin-4 antibody positive (Q41179) (← links)
- Recurrent optic neuritis aquaporin-4 antibody positive (Q41180) (← links)
- Recurrent transverse myelitis aquaporin-4 antibody positive (Q41181) (← links)
- Single optic neuritis aquaporin-4 antibody positive (Q41182) (← links)
- Neuromyelitis optica aquaporin-4 antibody positive (Q41183) (← links)
- Acute haemorrhagic leukoencephalitis (Q41184) (← links)
- Central demyelination of corpus callosum (Q41185) (← links)
- Central pontine myelinolysis (Q41186) (← links)
- Subacute necrotising myelitis (Q41187) (← links)
- Epilepsy due to degenerative brain disorders (Q41188) (← links)
- Epilepsy due to neonatal hypoxic ischemic encephalopathy (Q41189) (← links)
- 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)
