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TARA FRIEDMAN, M.D.
M.D.
Internal Medicine Physician
NPI: 1386772655Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
MD071180L(PA)
Hospice and Palliative Medicine (Internal Medicine) Physician
Internal Medicine — Hospice and Palliative Medicine
Code: 207RH0002X
52774(TN)036.139194(IL)212179(NY)C1-0011523(DE)25MA09959600(NJ)MD071180L(DC)D80611(MD)
Research & Publications (20)
Detection and incidence of anomalies associated with hypospadias.
PMID 18574601·Pediatr Nephrol·2008
8-other
[Diagnostic accuracy of skin lesions excised by a plastic surgeon].
PMID 18686810·Harefuah·2008
8-other
Rembrandt--aging and sickness: a combined look by plastic surgeons, an art researcher and an internal medicine specialist.
PMID 17348473·Isr Med Assoc J·2007
8-other
Predictors of A&E staff attitudes to self-harm patients who use self-laceration: influence of previous training and experience.
PMID 16516659·J Psychosom Res·2006
8-other
Self-inflicted garlic burns: our experience and literature review.
PMID 17040429·Int J Dermatol·2006
5-case
Generalized and mucosal melanosis associated with ultra-late recurrence of malignant melanoma.
PMID 11932801·Endoscopy·2002
5-case
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
PMID 19603065·Eur J Hum Genet·2010
8-other
Hair analysis provides a historical record of cortisol levels in Cushing's syndrome.
PMID 19609841·Exp Clin Endocrinol Diabetes·2010
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
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.
PMID 19650862·Clin Genet·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
Gamma-actin is required for cytoskeletal maintenance but not development.
PMID 19497859·Proc Natl Acad Sci U S A·2009
7-preclinical
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
PMID 19287372·J Hum Genet·2009
8-other
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
PMID 18505454·Clin 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
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
PMID 18953341·Nat Genet·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 41 UNIVERSITY DR, SUITE 400
NEWTOWN, PA 18940 - Phone
- (215) 375-7993
Quick Facts
- NPI
- 1386772655
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 8
- Locations
- 1
- Publications
- 20
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