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ELIZABETH TAUB, MD
MD
Anatomic Pathology & Clinical Pathology Physician
NPI: 1558550111Individual
Specialties, Licenses & Credentials
Anatomic Pathology & Clinical Pathology PhysicianPrimary
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
A62090(CA)
Research & Publications (20)
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
Improvement after constraint-induced movement therapy is independent of infarct location in chronic stroke patients.
PMID 19461024·Stroke·2009
8-other
Minimal detectable change scores for the Wolf Motor Function Test.
PMID 19498013·Neurorehabil Neural Repair·2009
8-other
Constraint-Induced Movement therapy can improve hemiparetic progressive multiple sclerosis. Preliminary findings.
PMID 18573826·Mult Scler·2008
3-trial
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
Potentiation of isometric and isotonic contractions during high-frequency stimulation.
PMID 18004591·Pflugers Arch·2008
7-preclinical
MRI infarction load and CI therapy outcomes for chronic post-stroke hemiparesis.
PMID 18431003·Restor Neurol Neurosci·2008
3-trial
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
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
PMID 18383588·Hum Genet·2007
8-other
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 18383587·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 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 18380023·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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1233 E 2ND ST
CASPER, WY 82601 - Phone
- (800) 288-8325
Quick Facts
- NPI
- 1558550111
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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