Assistant Professor, Neurology, Uniformed Services Hebert SOM
Neurology
Dr. Suzanne R. Lesage, MD
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Suzanne R. Lesage, MD works in the field of Neurology. She went to medical school at University of Colorado Denver School of Medicine. University of Colorado Denver School of Medicine is one of the top medical schools in the US. University of Colorado Denver School of Medicine is ranked 35/8 in Research/PrimaryCare. Dr. Suzanne R. Lesage is a published doctor and has 100 publications published. The lastest was: 'Autologous stem-cell transplantation for non-Hodgkin's lymphomas: the role of graft purging and radiotherapy posttransplantation--results of a retrospective analysis o...'
Publications
- PINK1 and FLNA mutations association: A role for atypical parkinsonism?
- PARKIN Inactivation Links Parkinson's Disease to Melanoma.
- Efficacy of subthalamic nucleus stimulation in C9ORF72 expansion related parkinsonism.
- De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
- Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's Disease (GEO-PD) consortium.
- Electroencephalographic hypersynchrony in a child with night terrors.
- G51D ?-synuclein mutation causes a novel parkinsonian-pyramidal syndrome.
- C9orf72 repeat expansions are a rare genetic cause of parkinsonism.
- Sleep disturbance in heavy marijuana users.
- Alteplase for hepatic veno-occlusive Disease complicating bone-marrow transplantation.
- Humic acid enhanced remediation of an emplaced diesel source in groundwater. 2. Numerical model development and application.
- Antagonism between Nur77 and glucocorticoid receptor for control of transcription.
- Novel dimeric Nur77 signaling mechanism in endocrine and lymphoid cells.
- Clinical applications of stem cell transfusion from cord blood.
- Characterization of lymphocyte subpopulations in cord blood.
- Preparation and successful engraftment of purified CD34+ bone marrow progenitor cells in patients with non-Hodgkin's lymphoma.
- Regenerative potential of silk conduits in repair of peripheral nerve injury in adult rats.
- A long-term follow-up of 33 patients with non-Hodgkin''s lymphoma who received the BEAM high-dose intensification regimen with cytokine support only and no transplant.
- The role of endoplasmic reticulum stress in nonimmune diabetes: NOD.k iHEL, a novel model of beta cell death.
- One hundred twenty-five adult patients with primary acute leukemia autografted with marrow purged by mafosfamide: a 10-year single institution experience.
- Cord-blood transplantation from an unrelated donor in an adult with chronic myelogenous leukemia.
- Treatment of adult chronic autoimmune thrombocytopenic purpura with repeated high-dose intravenous immunoglobulin.
- Bone marrow versus peripheral blood progenitor cells CD34 selection in patients with non-Hodgkin's lymphomas: different levels of tumor cell reduction. Implications fo...
- Genetic studies of the renin-angiotensin system in arterial hypertension associated with non-insulin-dependent diabetes mellitus.
- Autologous bone marrow transplantation with marrow purged by mafosfamide in seven patients with myelodysplastic syndromes in transformation (AML-MDS): a pilot study.
- What is sustainable remediation?
- Humic acids enhanced removal of aromatic hydrocarbons from contaminated aquifers: developing a sustainable technology.
- Progressive multifocal leucoencephalopathy with peripheral demyelinating neuropathy after autologous bone marrow transplantation for acute myeloblastic leukemia (FAB5).
- Autologous bone marrow transplantation as consolidation therapy may prolong remission in newly diagnosed high-risk follicular lymphoma: a pilot study of 34 cases.
- Improved efficiency of remission induction facilitates autologous BMT harvesting and improves overall survival in adults with AML: 108 patients treated at a single ins...
- Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairs.
- Genetic analyses of chromosome 12 loci in Crohn''s Disease.
- Search for DNA sequence variations using a MutS-based technology.
- Importance of marrow dose on posttransplant outcome in acute leukemia: models derived from patients autografted with mafosfamide-purged marrow at a single institution.
- Autologous stem-cell transplantation for non-Hodgkin's lymphomas: the role of graft purging and radiotherapy posttransplantation--results of a retrospective analysis o...
- LRRK2 mutations are uncommon in Turkey.
- Mutations in the glucocerebrosidase gene confer a risk for Parkinson Disease in North Africa.
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn''s Disease.
- Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson''s Disease.
- Two TaqI RFLPs at the GLUT2 locus in French Caucasian population.
- Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM.
- Retinal microvascular abnormalities and cognitive decline: the ARIC 14-year follow-up study.
- Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.
- Genetic analyses of glucose transporter genes in French non-insulin-dependent diabetic families.
- Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus.
- Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson Disease?
- Re: Alpha-synuclein gene duplication is present in sporadic Parkinson Disease.
- CARD4/NOD1 is not involved in inflammatory bowel Disease.
- CARD15 mutations in Blau syndrome.
- Linkage analysis and molecular scanning of glucokinase gene in NIDDM families.
- Rare heterozygous parkin variants in French early-onset Parkinson Disease patients and controls.
- A multidisciplinary study of patients with early-onset PD with and without parkin mutations.
- Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
- Etiology of the inflammatory bowel Diseases.
- LRRK2: a link between familial and sporadic Parkinson''s Disease?
- Low Disease risk in relatives of north african lrrk2 Parkinson Disease patients.
- Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus.
- Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel Disease.
- Deletion of the donor splice site of intron 4 in the glucokinase gene causes maturity-onset diabetes of the young.
- Multicenter analysis of glucocerebrosidase mutations in Parkinson's Disease.
- Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.
- Medication use in patients with restless legs syndrome compared with a control population.
- A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype.
- Effects of chlorinated solvents on four species of North American amphibians.
- Cognitive deficits associated with restless legs syndrome (RLS).
- The four diagnostic criteria for Restless Legs Syndrome are unable to exclude confounding conditions ("mimics").
- Polysomnogram changes in marijuana users who report sleep disturbances during prior abstinence.
- Role of Mendelian genes in "sporadic" Parkinson''s Disease.
- What genetics tells us about the causes and mechanisms of Parkinson's Disease.
- Association of LRRK2 exonic variants with susceptibility to Parkinson''s Disease: a case-control study.
- Role of sepiapterin reductase gene at the PARK3 locus in Parkinson''s Disease.
- Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson''s Disease.
- Imputation of sequence variants for identification of genetic risks for Parkinson''s Disease: a meta-analysis of genome-wide association studies.
- Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson''s Disease in the European population.
- Large-scale screening of the Gaucher''s Disease-related glucocerebrosidase gene in Europeans with Parkinson''s Disease.
- LRRK2 G2019S mutation in Parkinson''s Disease: a neuropsychological and neuropsychiatric study in a large Algerian cohort.
- Leucine-rich repeat kinase 2 is associated with the endoplasmic reticulum in dopaminergic neurons and accumulates in the core of Lewy bodies in Parkinson Disease.
- A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutations.
- Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson''s Disease: large-scale collaborative study.
- Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines.
- Assessing the prevalence of PINK1 genetic variants in South African patients diagnosed with early- and late-onset Parkinson's Disease.
- LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson''s Disease patients.
- Parkinson''s Disease-related LRRK2 G2019S mutation results from independent mutational events in humans.
- Pearls: sleep disorders.
- A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson''s Disease.
- Follow-up study of the GIGYF2 gene in French families with Parkinson''s Disease.
- From genes to proteins in mendelian Parkinson's Disease: an overview.
- Parkinson''s Disease: from monogenic forms to genetic susceptibility factors.
- Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms.
- CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel Disease.
- Construction and validation of a Parkinson's Disease mutation genotyping array for the Parkin gene.
- LRRK2 exon 41 mutations in sporadic Parkinson Disease in Europeans.
- Beyond the usual suspects: approaching sleep in elderly people.
- Bioremediation of tetrachloroethylene-contaminated groundwater in a model aquifer: effects on green frogs (Rana clamitans) and Xenopus laevis as potential wetland rece...
- Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson Disease pathogenesis.
- Subthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutations.
- Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism.
- Segregation analysis of restless legs syndrome: possible evidence for a major gene in a family study using blinded diagnoses.
- Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1.
Schools
UNIVERSITY OF COLORADO AT DENVER
McGaw Med Center Of Northwestern
University Of Co School Of Med
Conditions Treated
- Alzheimer's Disease
- Dementia
- Vertigo
Doctors Specialties
- Sleep Medicine
- Neurology
Accepted Insurances
Education
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McGaw Medical Center of Northwestern University -
University of Colorado -
University of Colorado Denver School of Medicine
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1356386569 |
| Last Name Of The Provider | LESAGE |
| First Name Of The Provider | SUZANNE |
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