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TALIA FRIEDMAN, M.D.
M.D.
Diagnostic Radiology Physician
NPI: 1518243211Individual
Specialties, Licenses & Credentials
Diagnostic Radiology PhysicianPrimary
Radiology — Diagnostic Radiology
Code: 2085R0202X
P79651(NY)
Research & Publications (20)
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
Self-inflicted garlic burns: our experience and literature review.
PMID 17040429·Int J Dermatol·2006
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
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
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
PMID 19287372·J Hum Genet·2009
8-other
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
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.
PMID 19646679·Am J Hum 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
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
PMID 18505454·Clin Genet·2009
8-other
[Diagnostic accuracy of skin lesions excised by a plastic surgeon].
PMID 18686810·Harefuah·2008
8-other
Cutaneous photodamage in schizophrenia patients.
PMID 19000185·Photodermatol Photoimmunol Photomed·2008
8-other
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.
PMID 18719945·Hum Genet·2008
8-other
Testosterone and bioavailable testosterone help to distinguish between mild Cushing's syndrome and polycystic ovarian syndrome.
PMID 18819057·Horm Metab Res·2008
8-other
Differential regulation of prohormone convertase 1/3, prohormone convertase 2 and phosphorylated cyclic-AMP-response element binding protein by short-term and long-term morphine treatment: implications for understanding the "switch" to opiate addiction.
PMID 18771713·Neuroscience·2008
7-preclinical
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
- 535 E 70TH ST, DEPARTMENT OF RADIOLOGY AND IMAGING
NEW YORK, NY 10021 - Phone
- (212) 606-1985
Quick Facts
- NPI
- 1518243211
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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