User profiles for N W Kowall
Neil KowallVA Boston, Boston University, Harvard Medical School Verified email at bu.edu Cited by 55559 |
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
The Alzheimer Disease Genetics Consortium (ADGC) performed a genome-wide association
study of late-onset Alzheimer disease using a three-stage design consisting of a discovery …
study of late-onset Alzheimer disease using a three-stage design consisting of a discovery …
The spectrum of disease in chronic traumatic encephalopathy
Chronic traumatic encephalopathy is a progressive tauopathy that occurs as a consequence
of repetitive mild traumatic brain injury. We analysed post-mortem brains obtained from a …
of repetitive mild traumatic brain injury. We analysed post-mortem brains obtained from a …
Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury
AG Reaume, JL Elliott, EK Hoffman, NW Kowall… - Nature …, 1996 - nature.com
The discovery that some cases of familial amyotrophic lateral sclerosis (FALS) are associated
with mutations in the gene encoding Cu/Zn superoxide dismutase (SOD1) has focused …
with mutations in the gene encoding Cu/Zn superoxide dismutase (SOD1) has focused …
Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid
Huntington's disease (HD) is an autosomal dominant neurological disorder characterized
by progressive chorea, cognitive impairment and emotional disturbance 1 . The disease …
by progressive chorea, cognitive impairment and emotional disturbance 1 . The disease …
Patterns of cell loss in Huntington's disease
NW Kowall, RJ Ferrante, JB Martin - Trends in Neurosciences, 1987 - cell.com
The key neuropathological features of Huntington's disease (HD) are neuronal loss and
astroglial proliferation in the striatum. Despite the lack of specificity of cell loss seen with …
astroglial proliferation in the striatum. Despite the lack of specificity of cell loss seen with …
Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid
…, BG Jenkins, RJ Ferrante, NW Kowall… - Journal of …, 1993 - Soc Neuroscience
An impairment of energy metabolism may underlie slow excitotoxic neuronal death in
neurodegenerative diseases. We therefore examined the effects of intrastriatal, subacute systemic, …
neurodegenerative diseases. We therefore examined the effects of intrastriatal, subacute systemic, …
[HTML][HTML] Epigenetic mechanisms of neurodegeneration in Huntington's disease
Huntington's disease (HD) is an incurable and fatal hereditary neurodegenerative disorder
of mid-life onset characterized by chorea, emotional distress, and progressive cognitive …
of mid-life onset characterized by chorea, emotional distress, and progressive cognitive …
Clinicopathological evaluation of chronic traumatic encephalopathy in players of American football
Importance Players of American football may be at increased risk of long-term neurological
conditions, particularly chronic traumatic encephalopathy (CTE). Objective To determine the …
conditions, particularly chronic traumatic encephalopathy (CTE). Objective To determine the …
Chronic traumatic encephalopathy in blast-exposed military veterans and a blast neurotrauma mouse model
Blast exposure is associated with traumatic brain injury (TBI), neuropsychiatric symptoms,
and long-term cognitive disability. We examined a case series of postmortem brains from US …
and long-term cognitive disability. We examined a case series of postmortem brains from US …
Selective sparing of a class of striatal neurons in Huntington's disease
A distinct subpopulation of striatal aspiny neurons, containing the enzyme nicotinamide
adenine dinucleotide phosphate diaphorase, is preserved in the caudate nucleus in …
adenine dinucleotide phosphate diaphorase, is preserved in the caudate nucleus in …