Pages that link to "Q46127870"
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The following pages link to Characteristics of established and proposed sporadic Creutzfeldt-Jakob disease variants (Q46127870):
Displaying 22 items.
- Young-onset dementia epidemiology applied to neuropsychiatry practice (Q28084429) (← links)
- Racial and ethnic differences in individuals with sporadic Creutzfeldt-jakob disease in the United States of America (Q28728294) (← links)
- Neuroradiology of human prion diseases, diagnosis and differential diagnosis (Q31155802) (← links)
- Interpretation of cerebrospinal fluid protein tests in the diagnosis of sporadic Creutzfeldt-Jakob disease: an evidence-based approach (Q33728522) (← links)
- Subtype and regional-specific neuroinflammation in sporadic creutzfeldt-jakob disease (Q33997514) (← links)
- The Creutzfeldt-Jakob disease (CJD) neurological status scale: a new tool for evaluation of disease severity and progression (Q35000257) (← links)
- "Dazed and diffused": making sense of diffusion abnormalities in neurologic pathologies (Q35027564) (← links)
- Recent US Case of Variant Creutzfeldt-Jakob Disease-Global Implications. (Q35546137) (← links)
- Rapidly progressive dementias and the treatment of human prion diseases (Q35832931) (← links)
- Evidence-based guideline: diagnostic accuracy of CSF 14-3-3 protein in sporadic Creutzfeldt-Jakob disease: report of the guideline development subcommittee of the American Academy of Neurology. (Q36475223) (← links)
- Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings (Q37053965) (← links)
- Specific clinical signs and symptoms are predictive of clinical course in sporadic Creutzfeldt-Jakob disease. (Q37385010) (← links)
- Fluid biomarkers for diagnosing dementia: rationale and the Canadian Consensus on Diagnosis and Treatment of Dementia recommendations for Canadian physicians (Q37693146) (← links)
- Sporadic Creutzfeldt-Jacob Disease: An 8-Year Experience from a Single Center in Turkey (Q37718090) (← links)
- Are synucleinopathies prion-like disorders? (Q37789524) (← links)
- Three sporadic cases of Creutzfeldt-Jakob disease in China and their clinical analysis (Q41671977) (← links)
- Progressive Stroke-Like Symptoms in a Patient with Sporadic Creutzfeldt-Jakob Disease (Q42593346) (← links)
- Variability in diagnosing Creutzfeldt-Jakob disease using standard and proposed diagnostic criteria (Q45076363) (← links)
- Comprehensive and Methodical: Diagnostic and Management Approaches to Rapidly Progressive Dementia (Q47891273) (← links)
- NMDA receptor autoantibodies in sporadic Creutzfeldt-Jakob disease (Q60049840) (← links)
- Alice in Wonderland Syndrome as a Presenting Manifestation of Creutzfeldt-Jakob Disease (Q64260877) (← links)
- Movement Disorders in Prionopathies: A Systematic Review (Q92221941) (← links)