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SAMANTHA KLEBE, DO
DO
Hospitalist Physician
NPI: 1649538844IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
74829(WI)OS017649(PA)
Hospitalist PhysicianPrimary
Hospitalist
Code: 208M00000X
74829(WI)
Education
OTHER
Class of 2012
Research & Publications (20)
Diagnosis of epithelial mesothelioma using tree-based regression analysis and a minimal panel of antibodies.
PMID 19152187·Pathology·2009
8-other
Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients.
PMID 19092771·Eur J Hum Genet·2009
8-other
Rejection and acceptance of corneal allografts.
PMID 19337139·Curr Opin Organ Transplant·2009
6-review
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia.
PMID 18855023·Neurogenetics·2009
8-other
Reduced surface tension normalizes static lung mechanics in a rodent chronic heart failure model.
PMID 19372252·Am J Respir Crit Care Med·2009
7-preclinical
Identification of LOXL1 protein and Apolipoprotein E as components of surgically isolated pseudoexfoliation material by direct mass spectrometry.
PMID 19442659·Exp Eye Res·2009
8-other
Evaluation of a screening instrument for essential tremor.
PMID 18381648·Mov Disord·2008
4-observational
Malignant mesothelioma with heterologous elements: clinicopathological correlation of 27 cases and literature review.
PMID 18587319·Mod Pathol·2008
8-other
Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots.
PMID 18191948·J Neurol Sci·2008
8-other
Another mutation in cysteine 131 in protein kinase C gamma as a cause of spinocerebellar ataxia type 14.
PMID 17562946·Arch Neurol·2007
5-case
Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families.
PMID 17661097·Neurogenetics·2007
5-case
A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21.
PMID 17515546·Neurology·2007
5-case
Resolution of primary acquired melanosis with atypia after minimal mitomycin C treatment.
PMID 18173419·Clin Exp Ophthalmol·2007
5-case
NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe.
PMID 17205300·Neurogenetics·2007
5-case
A novel locus for autosomal recessive spastic ataxia on chromosome 17p.
PMID 17273843·Hum Genet·2007
8-other
Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description.
PMID 17503452·Am J Med Genet B Neuropsychiatr Genet·2007
8-other
A randomized trial of deep-brain stimulation for Parkinson's disease.
PMID 16943402·N Engl J Med·2006
4-observational
Delayed surface opacification of a hydroview intraocular lens.
PMID 17026607·Clin Exp Optom·2006
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 3400 MINISTRY PKWY
WESTON, WI 54476 - Phone
- (715) 393-1000
Quick Facts
- NPI
- 1649538844
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 14
- Publications
- 20
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