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TIMOTHY FRIEDMAN, DO
DO
Family Medicine Physician
NPI: 1629414412Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
DO180033(OR)9408137(KS)5101021067(MI)
Research & Publications (20)
Hair analysis provides a historical record of cortisol levels in Cushing's syndrome.
PMID 19609841·Exp Clin Endocrinol Diabetes·2010
8-other
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
PMID 19603065·Eur J Hum Genet·2010
8-other
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
PMID 19287372·J Hum Genet·2009
8-other
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
Gamma-actin is required for cytoskeletal maintenance but not development.
PMID 19497859·Proc Natl Acad Sci U S A·2009
7-preclinical
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
PMID 18505454·Clin Genet·2009
8-other
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.
PMID 19646679·Am J Hum Genet·2009
8-other
Oral opioids for chronic non-cancer pain: higher prevalence of hypogonadism in men than in women.
PMID 18523930·Exp Clin Endocrinol Diabetes·2009
8-other
Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.
PMID 19250381·Clin Genet·2009
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 205 N EAST AVE
JACKSON, MI 49201 - Phone
- (517) 788-4800
Quick Facts
- NPI
- 1629414412
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 2
- Publications
- 20
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