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HENRY PAULSON, MD
MD
Neurology Physician
NPI: 1497748537IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
32013(IA)4301091125(MI)
CMS Specialties
PrimaryNEUROLOGY
Education
YALE UNIVERSITY SCHOOL OF MEDICINE
Class of 1990
Research & Publications (20)
In vivo suppression of polyglutamine neurotoxicity by C-terminus of Hsp70-interacting protein (CHIP) supports an aggregation model of pathogenesis.
PMID 19084066·Neurobiol Dis·2009
7-preclinical
Ubiquitination directly enhances activity of the deubiquitinating enzyme ataxin-3.
PMID 19153604·EMBO J·2009
7-preclinical
Allele-specific RNAi mitigates phenotypic progression in a transgenic model of Alzheimer's disease.
PMID 19532137·Mol Ther·2009
7-preclinical
X11alpha haploinsufficiency enhances Abeta amyloid deposition in Alzheimer's disease transgenic mice.
PMID 19631749·Neurobiol Dis·2009
7-preclinical
Polyglutamine neurodegeneration: protein misfolding revisited.
PMID 18778858·Trends Neurosci·2008
6-review
SOD1 mutations disrupt redox-sensitive Rac regulation of NADPH oxidase in a familial ALS model.
PMID 18219391·J Clin Invest·2008
7-preclinical
Obsessive and compulsive symptoms in prediagnosed Huntington's disease.
PMID 19012814·J Clin Psychiatry·2008
4-observational
Diversity in tissue expression, substrate binding, and SCF complex formation for a lectin family of ubiquitin ligases.
PMID 18203720·J Biol Chem·2008
7-preclinical
The deubiquitinating enzyme ataxin-3, a polyglutamine disease protein, edits Lys63 linkages in mixed linkage ubiquitin chains.
PMID 18599482·J Biol Chem·2008
8-other
Technology insight: therapeutic RNA interference--how far from the neurology clinic?
PMID 17611488·Nat Clin Pract Neurol·2007
6-review
Cellular turnover of the polyglutamine disease protein ataxin-3 is regulated by its catalytic activity.
PMID 17693639·J Biol Chem·2007
7-preclinical
Morphology of the cerebral cortex in preclinical Huntington's disease.
PMID 17728429·Am J Psychiatry·2007
4-observational
Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit.
PMID 17494702·J Neurosci·2007
7-preclinical
Dominantly inherited ataxias: lessons learned from Machado-Joseph disease/spinocerebellar ataxia type 3.
PMID 17390258·Semin Neurol·2007
6-review
Redox modifier genes in amyotrophic lateral sclerosis in mice.
PMID 17853944·J Clin Invest·2007
7-preclinical
Spinocerebellar ataxia type 3 (SCA3): thalamic neurodegeneration occurs independently from thalamic ataxin-3 immunopositive neuronal intranuclear inclusions.
PMID 16911479·Brain Pathol·2006
8-other
Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7.
PMID 17083478·Neuropathol Appl Neurobiol·2006
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4260 PLYMOUTH RD
ANN ARBOR, MI 48109 - Phone
- (734) 764-6831
Quick Facts
- NPI
- 1497748537
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 36
- Publications
- 20
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