Homozygous deletions of the CDKN2/p16 gene in dural hemangiopericytomas Yasuhiro OnoKeisuke UekiD. N. Louis Express communication Pages: 221 - 225
Filament heterogeneity within the dystrophic neurites of senile plaques suggests blockage of fast axonal transport in Alzheimer's disease Darja PraprotnikMark A. SmithG. Perry Regular paper Pages: 226 - 235
Temporal and spatial characterization of neuronal injury following lateral fluid-percussion brain injury in the rat R. HicksHolly SoaresTracy McIntosh Regular paper Pages: 236 - 246
Apolipoprotein E in Guamanian amyotrophic lateral sclerosis/ parkinsonism-dementia complex: genotype analysis and relationships to neuropathological changes L. BuéeJordi Pérez-TurP. R. Hof Regular paper Pages: 247 - 253
Neuronal and vascular pathology produced by verocytotoxin 2 in the rabbit central nervous system M. MizuguchiSoichiro TanakaMasao Miwa Regular paper Pages: 254 - 262
In situ hybridization analysis of Pit-1 mRNA and hormonal production in human pituitary adenomas N. SannoA. TeramotoR. Y. Osamura Regular paper Pages: 263 - 268
Glial fibrillary acidic protein-immunoreactive astrocytosis in elderly patients with schizophrenia and dementia S. E. ArnoldBryan R. FranzRaquel E. Gur Regular paper Pages: 269 - 277
Dendritic synapses of anterior horn neurons in amyotrophic lateral sclerosis: an ultrastructural study S. SasakiMakoto Iwata Regular paper Pages: 278 - 283
The expression of Galβ1,4GlcNAc α2,6 sialyltransferase and α2,6-linked sialoglycoconjugates in human brain tumors Yoichi KanekoHirotaka YamamotoJ. R. Moskal Regular paper Pages: 284 - 292
Molecular genetic alterations in pleomorphic xanthoastrocytoma Werner PaulusDavid K. LisleDavid N. Louis Regular paper Pages: 293 - 297
The M22 antibody identifies highly activated reactive astrocytes responding to central nervous system disease M. EddlestonJuan Carlos de la TorreM. B. A. Oldstone Regular paper Pages: 298 - 308
Severe cranial nerve involvement in longstanding demyelinating polyneuropathy: a clinicopathologic correlation Erin L. McCannT. W. SmithJane Sargent Case report Pages: 309 - 312
Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? – Pathological study of the cerebral cortex of an FCDM fetus I. NakanoMasuko FunahashiTatsushi Toda Case report Pages: 313 - 321
Partial block of glycolysis in late-onset phosphofructokinase deficiency myopathy R. MassaR. LodiG. Bernardi Case report Pages: 322 - 329