Back to Search
AJIT MANNAN, M.D.
M.D.
Internal Medicine Physician
NPI: 1659613719IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
A133177(CA)
Education
UNIVERSITY OF CALIFORNIA, GEFFEN SCHOOL OF MEDICINE
Class of 2013
Research & Publications (20)
Vascular hamartoma of the paranasal sinuses: report of 3 rare cases and a short review of the literature.
PMID 19172571·Ear Nose Throat J·2009
6-review
Sinus histiocytosis with massive lymphadenopathy (Rosai Dorfman disease): evidence for a dendritic cell derivation?
PMID 16761737·Indian J Pathol Microbiol·2005
8-other
Infantile fibromatosis of the nose and paranasal sinuses: report of a rare case and brief review of the literature.
PMID 15372920·Ear Nose Throat J·2004
5-case
Solitary malignant schwannoma of the nasal cavity and paranasal sinuses: report of two rare cases.
PMID 14503104·Ear Nose Throat J·2003
5-case
Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia.
PMID 18701882·Eur J Hum Genet·2009
8-other
Sall1, sall2, and sall4 are required for neural tube closure in mice.
PMID 18818376·Am J Pathol·2008
7-preclinical
Spastin oligomerizes into a hexamer and the mutant spastin (E442Q) redistribute the wild-type spastin into filamentous microtubule.
PMID 18410514·J Neurochem·2008
7-preclinical
Compound heterozygosity in the SPG4 gene causes hereditary spastic paraplegia.
PMID 18190593·Clin Genet·2008
8-other
Plasmacytoma of bronchus treated by radical radiotherapy--a rare case with four and a half years follow up.
PMID 17909364·J Thorac Oncol·2007
5-case
Facial motion analysis of acid burn victims--development of a new facial motion impairment index.
PMID 17374453·Burns·2007
8-other
From chloroquine to artemisinin-based combination therapy: the Sudanese experience.
PMID 16879742·Malar J·2006
8-other
ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia.
PMID 16826525·Am J Hum Genet·2006
4-observational
Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein.
PMID 16602018·Neurogenetics·2006
7-preclinical
Psychosocial outcomes derived from an acid burned population in Bangladesh, and comparison with Western norms.
PMID 16448773·Burns·2006
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
- 3330 LOMITA BLVD
TORRANCE, CA 90505 - Phone
- (310) 891-6623
Quick Facts
- NPI
- 1659613719
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 20
Are you this provider?
Claim Your Profile