Results 101 to 110 of about 13,613 (255)
Ataxias esporádicas de início no adulto: um desafio diagnóstico [PDF]
, 2014 Patients with adult onset non-familial progressive ataxia are classified in sporadic ataxia group. There are several disease categories that may manifest with sporadic ataxia: toxic causes, immune-mediated ataxias, vitamin deficiency, infectious diseases,
Albuquerque, Marcus Vinicius Cristino De +3 more
core +3 more sources
A 50 year old with a rapid neuropsychiatric deterioration and choreaform movements [PDF]
, 2017 A 50-year-old man presented acutely to the hospital with behavioural disturbance, choreiform movements and profound nihilistic delusions. He reported recent drug and alcohol abuse, and also apparent involvement in several recent criminal activities, for ...
Campbell, Stewart +3 more
core +1 more source
Neurobiology of Disease, 2014 Prion diseases are progressive disorders that affect the central nervous system leading to memory loss, personality changes, ataxia and neurodegeneration.
A. Murali, R.A. Maue, P.J. Dolph
doaj +1 more source
Human stem cell-derived astrocytes replicate human prions in a PRNP genotype-dependent manner. [PDF]
, 2017 Prions are infectious agents that cause neurodegenerative diseases such as Creutzfeldt-Jakob disease (CJD). The absence of a human cell culture model that replicates human prions has hampered prion disease research for decades.
Alibhai, James +9 more
core +1 more source
Rapidly Progressive Corticobasal Degeneration Syndrome
Case Reports in Neurology, 2011 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
Infectio, 2007 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
Avicenna Journal of Medicine, 2018 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
Creutzfeldt-Jakob Disease Patients with Congophilic Kuru Plaques Have the Missense Variant Prion Protein Common to Gerstmann-Straussler Syndrome [PDF]
, 1991 克美 堂浦 +2 more
openalex +1 more source
Prions: the danger of biochemical weapons [PDF]
, 2014 The knowledge of biotechnology increases the risk of using biochemical weapons for mass destruction. Prions are unprecedented infectious pathogens that cause a group of fatal neurodegenerative diseases by a novel mechanism.
Xavier, Eric Almeida
core +3 more sources