Results 111 to 120 of about 26,898 (212)
Oxidative and Inflammatory Events in Prion Diseases: Can They Be Therapeutic Targets? [PDF]
Prion diseases are a group of incurable infectious terminal neurodegenerative diseases caused by the aggregated misfolded PrPsc in selected mammals including humans.
Bondy, Stephen C, Prasad, Kedar N
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Neuroimaging biomarkers of neurodegenerative diseases and dementia [PDF]
Neurodegenerative disorders leading to dementia are common diseases that affect many older and some young adults. Neuroimaging methods are important tools for assessing and monitoring pathological brain changes associated with progressive ...
Risacher, Shannon L., Saykin, Andrew J.
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Rapidly Progressive Corticobasal Degeneration Syndrome
Introduction: Corticobasal syndrome (CBS) has a heterogeneous clinical presentation with no specific pathologic substratum. Its accurate diagnosis is a challenge for neurologists; in order to establish CBS definitively, postmortem confirmation is ...
Ana Herrero Valverde +4 more
doaj +1 more source
Se presenta el caso de una paciente de 65 años de edad con alucinaciones auditivas y visuales, rigidez en el hemicuerpo izquierdo que progresó al hemicuerpo derecho, con demostración por electroencefalograma de ondas trifásicas abundantes lentas ...
VILLAMIL WILMER +6 more
doaj
Creutzfeldt–Jakob disease with unusual presentation of peripheral neuropathy and ophthalmoplegia
Creutzfeldt–Jakob disease (CJD) is a well-described disease. It is characterized by rapidly progressive dementia, myoclonus, ataxia, pyramidal, and extrapyramidal signs.
Mais Arwani +3 more
doaj +1 more source
Sporadic Creutzfeldt-Jakob disease with unusual initial presentation as posterior reversible encephalopathy syndrome: a case report [PDF]
Edgaras Diržius +6 more
openalex +1 more source
Myoclonus is a movement disorder characterized by involuntary, sudden, brief muscle jerks caused by muscular contraction (positive myoclonus) or inhibition (negative myoclonus).1,2 Myoclonus is generally a medical sign and not a diagnosis.
Pavis Laengvejkal +2 more
doaj
MRI and clinical syndrome in dura materrelated Creutzfeldt-Jakob disease [PDF]
Bettina Meißner +12 more
openalex +1 more source
Imaging and clinical characteristics of sporadic Creutzfeldt-Jakob disease
Five patients with sporadic Creutzfeldt-Jakob disease (sCJD) presented rapidly progressive dementia which were subacute onset from 1 to 4 months. Among these cases, periodic synchronous discharge (PSD) of electroencephalography (EEG) was seen in 2 ...
Yan GAO +3 more
doaj
Paediatric Epilepsy Surgery Programme in Hong Kong: experience in Queen Mary Hospital / Duchess of Kent Children's Hospital [PDF]
Poster: no. P6BACKGROUND: Surgery is a well-established treatment for adults with intractable seizures. Increasingly, infants and children are being considered for epilepsy surgery.
Chan, PH +7 more
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