Back to Search
HASSAN SHAHIN, M.D.
M.D.
Nephrology Physician
NPI: 1770537870IndividualAccepts Medicare
Specialties, Licenses & Credentials
Nephrology PhysicianPrimary
Internal Medicine — Nephrology
Code: 207RN0300X
0101235884(VA)
Education
OTHER
Class of 1997
Research & Publications (14)
Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.
PMID 16385458·Am J Hum Genet·2006
4-observational
Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population.
PMID 16460646·Hum Genomics·2006
8-other
Monthly access flow monitoring with increased prophylactic angioplasty did not improve fistula patency.
PMID 16221240·Kidney Int·2005
8-other
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment.
PMID 15994881·J Med Genet·2005
4-observational
Cardiac involvement in patients with systemic lupus erythematosus and correlation of valvular lesions with anti-Ro/SS-A and anti-La/SS-B antibody levels.
PMID 17143660·Mod Rheumatol·2004
8-other
Symptomatic thrombotic events among Egyptian patients with systemic lupus erythematosus: special consideration for renal vein thrombosis.
PMID 12827401·Z Rheumatol·2003
8-other
Circulating interleukin-6, soluble interleukin-2 receptors, tumor necrosis factor alpha, and interleukin-10 levels in juvenile chronic arthritis: correlations with soft tissue vascularity assessed by power Doppler sonography.
PMID 12070682·Rheumatol Int·2002
8-other
From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30.
PMID 12032315·Proc Natl Acad Sci U S A·2002
7-preclinical
Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East.
PMID 11935342·Hum Genet·2002
8-other
Pulmonary function tests, high-resolution computerized tomography, alpha1-antitrypsin measurement, and early detection of pulmonary involvement in patients with systemic sclerosis.
PMID 11354564·Rheumatol Int·2001
8-other
The clinical patterns of myalgia in children with familial Mediterranean fever.
PMID 11071586·Semin Arthritis Rheum·2000
5-case
The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population.
PMID 10982182·Hum Genet·2000
8-other
The acute scrotum in Arab children with familial Mediterranean fever.
PMID 10663841·Pediatr Surg Int·2000
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
- 4141 DUKE ST
ALEXANDRIA, VA 22304 - Phone
- (703) 461-3556
Quick Facts
- NPI
- 1770537870
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 29
- Publications
- 14
Are you this provider?
Claim Your Profile