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Prevalence of cerebrospinal fluid Alzheimer disease-like pattern in atypical dementias
CSF Alzheimer Disease Atypical Dementias Frontotemporal Dementia Corticobasal Syndrome Progressive Supranuclear Palsy
2013/1/28
BACKGROUND: Differential diagnosis between Frontotemporal Dementia (FTD), Corticobasal Syndrome (CBS), Progressive Supranuclear Palsy Syndrome (PSP), FTD with motor neuron disease (FTD-MND) is often c...
Laser vision correction for patients with atypical topography of cornea, LASIK vs. PRK: A review
Refractive Laser Surgery PRK LASIK Atypical Topography Cornea Ectasia Keratoconus
2013/1/29
Purpose: To search evidence and determine whether PRK (Photo Refractive Keratectomy) or LASIK (Laser in Situ Keratomileusis) produce a better outcome of laser vision correction for patients with atypi...
Cold agglutinin disease associated with mycoplasma infection in an individual with type 2 diabetes: An atypical case
Cold Agglutinin Disease Diabetes Mellitus Mycoplasma
2013/1/30
Cold Agglutinin Disease is a hemolytic anemia associated with cold reactive autoantibodies. Although the acute form of cold agglutinin disease can be attributed to autoimmune or infectious diseases an...
HIV-complicated meningovascular syphilis: Atypical symptoms with promising result using low molecular weight heparin
Meningovascular Syphilis HIV
2013/2/20
Both WHO and the CDC of Taiwan have reports indicating a dramatic increase in incidence of both syphilis and HIV. With their co-infection, neurosyphilis will become a major issue, and meningovascular ...
Atypical Small Hemangiomas of the Liver：Hypervascular Hemangiomas
hypervascular hemangioma CT scan MRI
2009/4/20
Hyperdynamic hemangiomas (HH) are atypical hepatic hemangiomas with an incidence of approximately 16% of all hemangiomas in the liver. We report a case of HH in a 47-year-old woman. Multiphase helical...
Wilson Disease Patients with Atypical Psychiatric Symptoms
Wilson disease inborn error of copper metabolism psychiatric symptoms hallucination autosmia
2009/3/16
Wilson disease is an autosomal recessive disorder of copper metabolism. The disease phenotype includes chronic liver disease (cirrhosis), neurological impairment (extra pyramidal signs), Kayser-Fleisc...