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CHRISTOPHER SUE, MD
MD
Family Medicine Physician
NPI: 1639730799IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
74223-20(WI)18008(ND)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Education
OTHER
Class of 2019
Research & Publications (20)
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2.
PMID 10805329·Ann Neurol·2000
8-other
Classification and mass production technique for three-quarter shoe insoles using non-weight-bearing plantar shapes.
PMID 18620334·Appl Ergon·2009
8-other
Mitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian community.
PMID 19086081·Mov Disord·2009
8-other
Prevalence of mitochondrial 1555A-->G mutation in adults of European descent.
PMID 19196685·N Engl J Med·2009
8-other
Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration.
PMID 19434233·PLoS One·2009
8-other
Characterization of 2-deoxy-D-glucose uptake in fibroblast cultures derived from patients with A3243G mitochondrial DNA mutation.
PMID 19058615·Southeast Asian J Trop Med Public Health·2008
8-other
Functional secretion of a type 1 antifreeze protein analogue by optimization of promoter, signal peptide, prosequence, and terminator in Lactococcus lactis.
PMID 18759446·J Agric Food Chem·2008
8-other
Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease.
PMID 17427941·Mov Disord·2007
8-other
Population prevalence and incidence of Parkinson's disease in an Australian community.
PMID 17561942·Intern Med J·2007
8-other
Mitochondrial DNA haplogroups and age-related hearing loss.
PMID 17875861·Arch Otolaryngol Head Neck Surg·2007
8-other
Mitochondrial disease mimicking Charcot-Marie Tooth disease.
PMID 17172573·J Neurol Neurosurg Psychiatry·2007
5-case
Supplemental oxygen and muscle metabolism in mitochondrial myopathy patients.
PMID 17219172·Eur J Appl Physiol·2007
2-rct
A functional polymorphism in the parkin gene promoter affects the age of onset of Parkinson's disease.
PMID 17280783·Neurosci Lett·2007
8-other
Exercise and myotonic dystrophy: a 31P magnetic resonance spectroscopy and magnetic resonance imaging case study.
PMID 16634010·Ann Neurol·2006
5-case
Prevalence of mitochondrial DNA haplogroups in an Australian population.
PMID 16866660·Intern Med J·2006
4-observational
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
- 2400 W VILLARD AVE, WFHC GLENDALE FAMILY CENTER
MILWAUKEE, WI 53209 - Phone
- (414) 527-8191
Quick Facts
- NPI
- 1639730799
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 7
- Publications
- 20
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