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DR. EUGENE NORMAN TAUB D.O.
D.O.
Addiction Psychiatry Physician
NPI: 1164758975Individual
Specialties, Licenses & Credentials
Addiction Psychiatry PhysicianPrimary
Psychiatry & Neurology — Addiction Psychiatry
Code: 2084P0802X
30275(MO)
Research & Publications (20)
Minimal detectable change scores for the Wolf Motor Function Test.
PMID 19498013·Neurorehabil Neural Repair·2009
8-other
Improvement after constraint-induced movement therapy is independent of infarct location in chronic stroke patients.
PMID 19461024·Stroke·2009
8-other
A method for standardizing procedures in rehabilitation: use in the extremity constraint induced therapy evaluation multisite randomized controlled trial.
PMID 19345784·Arch Phys Med Rehabil·2009
4-observational
Potentiation of isometric and isotonic contractions during high-frequency stimulation.
PMID 18004591·Pflugers Arch·2008
7-preclinical
Poststroke cerebral peduncular atrophy correlates with a measure of corticospinal tract injury in the cerebral hemisphere.
PMID 18024577·AJNR Am J Neuroradiol·2008
8-other
Retention of upper limb function in stroke survivors who have received constraint-induced movement therapy: the EXCITE randomised trial.
PMID 18077218·Lancet Neurol·2008
2-rct
Genetic carrier screening for spinal muscular atrophy and spinal muscular atrophy with respiratory distress 1 in an isolated population in Israel.
PMID 18298318·Genet Test·2008
8-other
Remodeling the brain: plastic structural brain changes produced by different motor therapies after stroke.
PMID 18323492·Stroke·2008
2-rct
MRI infarction load and CI therapy outcomes for chronic post-stroke hemiparesis.
PMID 18431003·Restor Neurol Neurosci·2008
3-trial
Constraint-Induced Movement therapy can improve hemiparetic progressive multiple sclerosis. Preliminary findings.
PMID 18573826·Mult Scler·2008
3-trial
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383589·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383590·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383591·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383593·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383594·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383595·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383596·Hum Genet·2007
8-other
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383597·Hum Genet·2007
8-other
Extending the Constraint-Induced Movement Therapy (CIMT) approach to cognitive functions: Constraint-Induced Aphasia Therapy (CIAT) of chronic aphasia.
PMID 17971622·NeuroRehabilitation·2007
6-review
Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel.
PMID 17149387·Eur J Hum Genet·2007
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
- 900 E CHERRY ST
TROY, MO 63379 - Phone
- (636) 528-8585
Quick Facts
- NPI
- 1164758975
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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