Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs
Humanin detected in skeletal muscles of MELAS patients
Tuft-shaped astrocytes in Lewy body disease
Secretoglobins in the human pituitary
Losses of chromosomes 1p and 19q are rare in pediatric oligodendrogliomas
OPA1, associated with autosomal dominant optic atrophy, is widely expressed in the human brain
Interneuron deficits in patients with the Miller-Dieker syndrome
A new murine model of giant proximal axonopathy
The enlarging spectrum of desminopathies
Redistribution of the water channel protein aquaporin-4 and the K+ channel protein Kir4.1 differs in low- and high-grade human brain tumors
Extending the clinicopathological spectrum of neurofilament inclusion disease
Congenital disorder of glycosylation type Ia
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene ( PRNP ) and a 17-kDa prion protein fragment
Fulminant inflammatory leukoencephalopathy associated with HAART-induced immune restoration in AIDS-related progressive multifocal leukoencephalopathy
Kurt Jellinger Prize for Outstanding Scientific Writing in Neuropathology