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KENNETH YEW, MD

MD

Family Medicine Physician

NPI: 1396717419IndividualAccepts Medicare

Specialties, Licenses & Credentials

Family Medicine PhysicianPrimary

Family Medicine

Code: 207Q00000X

68146(WI)ME 79400(FL)01092539A(IN)

CMS Specialties

PrimaryFAMILY PRACTICE

Education

MICHIGAN STATE UNIVERSITY COLLEGE OF HUMAN MEDICINE

Class of 1989

Research & Publications (20)

Teaching evidence-based medicine skills: an exploratory study of residency graduates' practice habits.
PMID 18172795·Fam Med·2008
8-other
Acute stroke diagnosis.
PMID 19621844·Am Fam Physician·2009
6-review
Contact lenses in pediatrics study in Singapore.
PMID 19516144·Eye Contact Lens·2009
4-observational
Clinical inquiries: are there any known health risks to early introduction of solids to an infant's diet?
PMID 19358803·J Fam Pract·2009
8-other
Diagnosis of chronic obstructive pulmonary disease.
PMID 18649615·Am Fam Physician·2008
6-review
Elephant shark sequence reveals unique insights into the evolutionary history of vertebrate genes: A comparative analysis of the protocadherin cluster.
PMID 18319338·Proc Natl Acad Sci U S A·2008
4-observational
Sequencing and comparative analysis of fugu protocadherin clusters reveal diversity of protocadherin genes among teleosts.
PMID 17394664·BMC Evol Biol·2007
4-observational
PINK1 mutations in sporadic early-onset Parkinson's disease.
PMID 16482571·Mov Disord·2006
5-case
Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition: clinical association.
PMID 16244875·Hum Genet·2005
8-other
Analysis of PINK1 in Asian patients with familial parkinsonism.
PMID 16207217·Clin Genet·2005
8-other
Differential expression of splice variant and wild-type parkin in sporadic Parkinson's disease.
PMID 16086186·Neurogenetics·2005
8-other
Cross-talk between bone morphogenetic protein and transforming growth factor-beta signaling is essential for exendin-4-induced insulin-positive differentiation of AR42J cells.
PMID 16020542·J Biol Chem·2005
7-preclinical
Functional COMT variant predicts response to high dose pyridoxine in Parkinson's disease.
PMID 15965967·Am J Med Genet B Neuropsychiatr Genet·2005
3-trial
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.
PMID 15955629·Neurosci Lett·2005
3-trial
Expanded FMR1 alleles are rare in idiopathic Parkinson's disease.
PMID 15742217·Neurogenetics·2005
8-other
Alpha-synuclein mRNA expression in sporadic Parkinson's disease.
PMID 15719423·Mov Disord·2005
8-other
Analysis of MDR1 haplotypes in Parkinson's disease in a white population.
PMID 15542248·Neurosci Lett·2004
8-other
Interplay of glucagon-like peptide-1 and transforming growth factor-beta signaling in insulin-positive differentiation of AR42J cells.
PMID 15504962·Diabetes·2004
7-preclinical
Nurr1 mutational screen in Parkinson's disease.
PMID 15390059·Mov Disord·2004
8-other
Genetic analysis of DJ-1 in a cohort Parkinson's disease patients of different ethnicity.
PMID 15308309·Neurosci Lett·2004
4-observational

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
1818 CAREW ST STE 120
FORT WAYNE, IN 46805

Location

Practice Location

1818 CAREW ST STE 120, FORT WAYNE, IN
(260) 425-6200

Quick Facts

NPI
1396717419
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
3
Locations
1
Years in Practice
37
Publications
20

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