Back to Search
THEODORE FRIEDMAN, M.D.
M.D.
Anatomic Pathology & Clinical Pathology Physician
NPI: 1164608451IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anatomic Pathology & Clinical Pathology PhysicianPrimary
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
0101249423(VA)
CMS Specialties
PrimaryPATHOLOGY
Education
GEISEL SCHOOL OF MEDICINE AT DARTMOUTH
Class of 2003
Clinical Trials (1)
1
Linked Trials
0
Recruiting
1
With Results
Research & Publications (20)
Evolution of responding CD4+ and CD8+ T-cell repertoires during the development of graft-versus-host disease directed to minor histocompatibility antigens.
PMID 15077221·Biol Blood Marrow Transplant·2004
7-preclinical
Vbeta spectratype analysis reveals heterogeneity of CD4+ T-cell responses to minor histocompatibility antigens involved in graft-versus-host disease: correlations with epithelial tissue infiltrate.
PMID 11215694·Biol Blood Marrow Transplant·2001
7-preclinical
Nonmyeloablative conditioning allows for more rapid T-cell repertoire reconstitution following allogeneic matched unrelated bone marrow transplantation compared to myeloablative approaches.
PMID 11787528·Biol Blood Marrow Transplant·2001
4-observational
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
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
PMID 19287372·J Hum 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
DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.
PMID 19650862·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
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
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
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
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
Green pay dirt. Why strategies to tackle climate change will boost the economy.
PMID 18847079·Sci Am·2008
8-other
Cutaneous photodamage in schizophrenia patients.
PMID 19000185·Photodermatol Photoimmunol Photomed·2008
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
- 3600 JOSEPH SIEWICK DR
FAIRFAX, VA 22033 - Phone
- (703) 391-3654
Quick Facts
- NPI
- 1164608451
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 23
- Clinical Trials
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile