Brent T. Harris

Propionic acidemia: a neuropathology case report and review of prior cases.

Acute monocular blindness resulting from transformation of von Recklinghausen's neurofibromatosis to malignant melanocytic schwannomas.

Dopamine efflux in the rat striatum evoked by electrical stimulation of the subthalamic nucleus: potential mechanism of action in Parkinson's disease.

Calretinin expression in tumors of adipose tissue.

Hypertrophy of Pacinian corpuscles in a young patient with neurofibromatosis.

Induction of astrocyte differentiation by propentofylline increases glutamate transporter expression in vitro: heterogeneity of the quiescent phenotype.

A fatal case of postpartum cerebral angiopathy with literature review.

Discussion of the pathology of giant cell arteritis.

Propofol-associated fatal myocardial failure and rhabdomyolysis in an adult with status epilepticus.

Oncogenic regulators and substrates of the anaphase promoting complex/cyclosome are frequently overexpressed in malignant tumors.

Does treating schizophrenia reduce the chances of developing amyotrophic lateral sclerosis?

Formation of native prions from minimal components in vitro.

Selective incorporation of polyanionic molecules into hamster prions.

Differential regulation of neuregulin 1 expression by progesterone in astrocytes and neurons.

Cellular genesis in the postnatal piglet.

The effects of prion protein proteolysis and disaggregation on the strain properties of hamster scrapie.

Spinal glioma: platelet-derived growth factor B-mediated oncogenesis in the spinal cord.

Id2 is required for specification of dopaminergic neurons during adult olfactory neurogenesis.

Prion protein glycosylation is not required for strain-specific neurotropism.

Scaled cortical impact in immature swine: effect of age and gender on lesion volume.

Cerebellar loss and brain-stem atrophy associated with neonatal alloimmune thrombocytopenia in a discordant twin.

Rosette-forming glioneuronal tumor.

Trans-dominant inhibition of prion propagation in vitro is not mediated by an accessory cofactor.

Estimation of brain deformation for volumetric image updating in protoporphyrin IX fluorescence-guided resection.

Efficacy of thalidomide for the treatment of amyotrophic lateral sclerosis: a phase II open label clinical trial.

A cluster of amyotrophic lateral sclerosis in New Hampshire: a possible role for toxic cyanobacteria blooms.

Multifactor dimensionality reduction for graphics processing units enables genome-wide testing of epistasis in sporadic ALS.

Progressive changes in microglia and macrophages in spinal cord and peripheral nerve in the transgenic rat model of amyotrophic lateral sclerosis.

ACAT1 gene ablation increases 24(S)-hydroxycholesterol content in the brain and ameliorates amyloid pathology in mice with AD.

Coregistered fluorescence-enhanced tumor resection of malignant glioma: relationships between δ-aminolevulinic acid-induced protoporphyrin IX fluorescence, magnetic resonance imaging enhancement, and neuropathological parameters. Clinical article.

Synthetic triterpenoid CDDO derivatives modulate cytoprotective or immunological properties in astrocytes, neurons, and microglia.

In situ photodegradation of incorporated polyanion does not alter prion infectivity.

Confocal microscopy for the histological fluorescence pattern of a recurrent atypical meningioma: case report.

Quantitative fluorescence in intracranial tumor: implications for ALA-induced PpIX as an intraoperative biomarker.

Essential muscle pathology for the rheumatologist.

Primary melanoma of the spinal cord: a case report, molecular footprint, and review of the literature.

Mucolipidosis type III α/β: the first characterization of this rare disease by autopsy.

Quantitative and qualitative 5-aminolevulinic acid-induced protoporphyrin IX fluorescence in skull base meningiomas.

δ-aminolevulinic acid-induced protoporphyrin IX concentration correlates with histopathologic markers of malignancy in human gliomas: the need for quantitative fluorescence-guided resection to identify regions of increasing malignancy.

Mutational inactivation of STAG2 causes aneuploidy in human cancer.

Strain-dependent variation in the early transcriptional response to CNS injury using a cortical explant system.

Genetics of glioblastoma: a window into its imaging and histopathologic variability.

A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations.

Combined fluorescence and reflectance spectroscopy for in vivo quantification of cancer biomarkers in low- and high-grade glioma surgery.

Spatial clustering of amyotrophic lateral sclerosis and the potential role of BMAA.

Anti-inflammatory efficacy of dexamethasone and Nrf2 activators in the CNS using brain slices as a model of acute injury.

Coexisting adult polyglucosan body disease with frontotemporal lobar degeneration with transactivation response DNA-binding protein-43 (TDP-43)-positive neuronal inclusions.

Glioblastoma multiforme treatment with clinical trials for surgical resection (aminolevulinic acid).

Gene ontology analysis of pairwise genetic associations in two genome-wide studies of sporadic ALS.

Neuron-specific enolase, but not S100B or myelin basic protein, increases in peripheral blood corresponding to lesion volume after cortical impact in piglets.

Gadolinium- and 5-aminolevulinic acid-induced protoporphyrin IX levels in human gliomas: an ex vivo quantitative study to correlate protoporphyrin IX levels and blood-brain barrier breakdown.

Adjuncts for maximizing resection: 5-aminolevuinic acid.

Purification and culture of spinal motor neurons.

Purification and culture of spinal motor neurons from rat embryos.

Infrastructure resources for clinical research in amyotrophic lateral sclerosis.

5-Aminolevulinic acid-induced protoporphyrin IX fluorescence in meningioma: qualitative and quantitative measurements in vivo.

Maturation-dependent response of neurogenesis after traumatic brain injury in children.

Molecular characterization of choroid plexus tumors reveals novel clinically relevant subgroups.