Results 71 to 80 of about 29,744 (185)
Creutzfeldt‐Jakob‐Like Presentation in Anti‐AMPAR Encephalitis
Annals of Neurology, EarlyView.
Kate Durbano +3 more
wiley +1 more source
Vox Sanguinis, EarlyView.Abstract Background and Objectives Adequate representation of donors from diverse ancestral populations in blood, stem cell and organ transplantation is critical to ensuring equitable access to these lifesaving therapies. Because of population‐level differences in genetic markers, patients from racialized groups may have unique transfusion and ...
Bonnie Lu +9 more
wiley +1 more source
Sporadic Creutzfeldt–Jakob Disease
Acta Medica BulgaricaSporadic Creutzfeldt–Jakob disease is a rare and fatal human prion disease characterized by a rapidly progressive dementia, myoclonus, cerebellar, pyramidal, extrapyramidal, visual, and psychiatric symptoms. These findings are all non-specific and making
Zhelyazkova S. +3 more
doaj +1 more source
Probable sporadic Creutzfeldt–Jakob disease mimicking focal epilepsy
Epilepsy and Behavior Case Reports, 2019 Creutzfeldt–Jakob disease (CJD) presents with seizures as an early symptom in only approximately 3% of cases. These seizures often present as nonconvulsive status epilepticus (NCSE) or epilepsia partialis continua (EPC).
Pei-Shan Hsiao +5 more
doaj +1 more source
Journal of Human Nutrition and Dietetics, Volume 39, Issue 3, June 2026.ABSTRACT Aim Neurodegenerative diseases and disordered eating have become rapidly expanding areas of research. However, research addressing the relationship between the two is lacking. Methods A scoping review guided by the Joanna Briggs Institute methodological framework was completed to synthesise the evidence related to disordered eating behaviours ...
Emily Buttifant +2 more
wiley +1 more source
Case Reports in Neurological Medicine, 2018 Sporadic Creutzfeldt-Jakob disease (sCJD) is a type of progressive, subacute encephalopathy associated with spongiform degeneration of the central nervous system.
Sira Carrasco García de León +3 more
doaj +1 more source
Understanding the Phenotypic Heterogeneity Within the Sporadic Creutzfeldt–Jakob Disease MV1 Subtype
Neuropathology and Applied Neurobiology, Volume 52, Issue 3, June 2026.We present the clinical, pathological and prion biophysical features of three atypical cases of the MV1 subtype of sporadic Creutzfeldt–Jakob disease (sCJD). We propose that these heterozygous cases exist on a spectrum ranging from MM1‐like to VV1‐like phenotypes and recommend that subtyping be performed at pH 6.9 to avoid missing atypical or mixed ...
Satish K. Nemani +6 more
wiley +1 more source
BSE crisis and food safety regulation: a comparison of the UK and Germany [PDF]
, 2007 The BSE crisis represents one of the worst policy disasters experienced by a UK government in recent years. In material terms, it led to the slaughter of 3.3 million cattle and an estimated economic loss of £3.7 billion.
Asenova, D., Beck, M., Kewell, B.
core +3 more sources
Sporadic Creutzfeldt‐Jakob disease: A case report and review of literature
Clinical Case Reports, 2020 Creutzfeldt‐Jakob Disease is a rare neurodegenerative disease and earlier diagnosis is usually difficult. Combining clinical features with electroencephalogram, laboratory parameters, and neuroimaging findings will facilitate the diagnosis.
Rajeev Ojha +5 more
doaj +1 more source
Bibliometric analysis of Alzheimer's and dementia research in Latin America
Alzheimer's &Dementia, Volume 22, Issue 5, May 2026.Abstract INTRODUCTION Dementia is increasing rapidly in Latin America and the Caribbean (LAC), but research output remains limited. Tracking publication trends, themes, and collaborations is key to guiding regional research and policy. METHODS Bibliometric analysis was conducted on dementia‐related publications from 21 LAC countries (1990 to 2024 ...
Mauricio Vazquez‐Guajardo +7 more
wiley +1 more source