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SUZANNE LESAGE, M.D.
M.D.
Neurology Physician
NPI: 1356386569Individual
Specialties, Licenses & Credentials
Sleep Medicine (Psychiatry & Neurology) Physician
Psychiatry & Neurology — Sleep Medicine
Code: 2084S0012X
53259(CO)
Specialist
Specialist
Code: 174400000X
D0058093(MD)
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
53259(CO)
Research & Publications (20)
Humic acids enhanced removal of aromatic hydrocarbons from contaminated aquifers: developing a sustainable technology.
PMID 11597111·J Environ Sci Health A Tox Hazard Subst Environ Eng·2001
4-observational
Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study.
PMID 19475631·Am J Med Genet B Neuropsychiatr Genet·2010
1-meta
Low-dose fentanyl-midazolam combination improves sevoflurane induction in adults.
PMID 19641980·Can J Anaesth·2009
2-rct
Absence of CD47 in vivo influences thymic dendritic cell subset proportions but not negative selection of thymocytes.
PMID 19147837·Int Immunol·2009
7-preclinical
A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutations.
PMID 19617340·J Nucl Med·2009
8-other
Parkinson's disease: from monogenic forms to genetic susceptibility factors.
PMID 19297401·Hum Mol Genet·2009
6-review
A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype.
PMID 19172321·Neurogenetics·2009
8-other
The four diagnostic criteria for Restless Legs Syndrome are unable to exclude confounding conditions ("mimics").
PMID 19185537·Sleep Med·2009
8-other
Cutting edge: genetic characterization of IFN-producing killer dendritic cells.
PMID 19380763·J Immunol·2009
7-preclinical
Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms.
PMID 19139307·Arch Neurol·2009
8-other
A multidisciplinary study of patients with early-onset PD with and without parkin mutations.
PMID 18987353·Neurology·2009
8-other
Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease.
PMID 19357115·J Med Genet·2009
8-other
A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations.
PMID 18718805·Parkinsonism Relat Disord·2009
8-other
Cutting edge: CD47 controls the in vivo proliferation and homeostasis of peripheral CD4+ CD25+ Foxp3+ regulatory T cells that express CD103.
PMID 18832672·J Immunol·2008
7-preclinical
Re: Alpha-synuclein gene duplication is present in sporadic Parkinson disease.
PMID 18852449·Neurology·2008
5-case
Are parkin patients particularly suited for deep-brain stimulation?
PMID 18228569·Mov Disord·2008
8-other
Gene symbol: PARK2. Disease: Parkinsonism, juvenile, autosomal recessive.
PMID 18386383·Hum Genet·2008
8-other
The infevers autoinflammatory mutation online registry: update with new genes and functions.
PMID 18409191·Hum Mutat·2008
8-other
Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?
PMID 18981379·Neurology·2008
8-other
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
- 1000 RUSH DR
SALIDA, CO 81201 - Phone
- (719) 530-2000
Quick Facts
- NPI
- 1356386569
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 2
- Publications
- 20
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