User profiles for N W Kowall

Neil Kowall

VA 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

…, A Karydas, JA Kaye, R Kim, EH Koo, NW Kowall… - Nature …, 2011 - nature.com
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 …

The spectrum of disease in chronic traumatic encephalopathy

…, BL Wolozin, AE Budson, LE Goldstein, NW Kowall… - Brain, 2013 - academic.oup.com
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 …

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 …

Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid

MF Beal, NW Kowall, DW Ellison, MF Mazurek… - Nature, 1986 - nature.com
Huntington's disease (HD) is an autosomal dominant neurological disorder characterized
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 …

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, …

[HTML][HTML] Epigenetic mechanisms of neurodegeneration in Huntington's disease

J Lee, YJ Hwang, KY Kim, NW Kowall, H Ryu - Neurotherapeutics, 2013 - Elsevier
Huntington's disease (HD) is an incurable and fatal hereditary neurodegenerative disorder
of mid-life onset characterized by chorea, emotional distress, and progressive cognitive …

Clinicopathological evaluation of chronic traumatic encephalopathy in players of American football

…, PH Montenigro, CE Chaisson, Y Tripodis, NW Kowall… - Jama, 2017 - jamanetwork.com
Importance Players of American football may be at increased risk of long-term neurological
conditions, particularly chronic traumatic encephalopathy (CTE). Objective To determine the …

Chronic traumatic encephalopathy in blast-exposed military veterans and a blast neurotrauma mouse model

…, T Ikezu, TD Stein, AE Budson, NW Kowall… - Science translational …, 2012 - science.org
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 …

Selective sparing of a class of striatal neurons in Huntington's disease

RJ Ferrante, NW Kowall, MF Beal, EP Richardson Jr… - Science, 1985 - science.org
A distinct subpopulation of striatal aspiny neurons, containing the enzyme nicotinamide
adenine dinucleotide phosphate diaphorase, is preserved in the caudate nucleus in …