Results 261 to 270 of about 12,440,936 (400)

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra   +17 more
wiley   +1 more source

Ureteral involvement in xanthogranulomatous pyelonephritis- Rare manifestation

open access: yesIndian Journal of Radiology and Imaging, 2006
S Sharma   +4 more
doaj   +1 more source

Bone mineral density predicts survival in patients with hepatocellular carcinoma and portal vein tumor thrombosis. [PDF]

open access: yesPLoS One
Müller L   +15 more
europepmc   +1 more source

3D MRI Tract‐Specific Spinal Cord Lesion Pattern Improves Prediction of Distinct Neurological Recovery

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To distinguish lateralized motor‐ and sensory‐tract damage after acute spinal cord injury (SCI) and explore its predictive power for motor and sensory recovery. Methods Thirty‐five SCI patients (two female) from a multi‐center data set (placebo‐arm of the Nogo‐A‐Inhibition in SCI trial) underwent routine T2‐weighted sagittal MRI ...
Lynn Farner   +7 more
wiley   +1 more source

Risk factors for delayed diagnosis of endometrial cancer among black individuals: Results from the GUIDE-EC study. [PDF]

open access: yesGynecol Oncol Rep
Gross ME   +10 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy