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RINKU PARMAR, DMD
DMD
Endodontics
NPI: 1821221573Individual
Specialties, Licenses & Credentials
EndodonticsPrimary
Dentist — Endodontics
Code: 1223E0200X
DS035533(PA)GI 0001293(DE)
Research & Publications (20)
Grain size dependent transport and magnetoresistance behavior of chemical solution deposition grown nanostructured La0.7Sr0.3MnO3 manganite films.
PMID 19049192·J Nanosci Nanotechnol·2008
8-other
Viscerohepatodiaphragmatic interposition (Chilaiditi's syndrome) in a child.
PMID 15200206·J Indian Med Assoc·2004
5-case
A prospective, randomised, double-blind study of comparative efficacy of immediate versus daily cleaning of stethoscope using 66% ethyl alcohol.
PMID 15523163·Indian J Med Sci·2004
3-trial
A newly recognized syndrome with double upper and lower lip, hypertelorism, eyelid ptosis, blepharophimosis, and third finger clinodactyly.
PMID 14699621·Am J Med Genet A·2004
5-case
Ring chromosome 12 with variable phenotypic features: clinical report and review of the literature.
PMID 12599192·Am J Med Genet A·2003
5-case
Necrotizing myelitis in an immunocompetent child: a case report with review of literature.
PMID 14701948·Indian J Med Sci·2003
5-case
Primary intraventricular haemorrhage: a rare presenting feature of arteriovenous malformation in children.
PMID 12405340·J Indian Med Assoc·2002
5-case
Measles encephalitis: a report of two cases with variable manifestations.
PMID 11982880·Pediatr Int·2002
5-case
Thoracic epidural neurilemmoma: a rare cause of childhood paraparesis.
PMID 11224588·Indian Pediatr·2001
5-case
Factor X deficiency and hemophilia A : occurrence of two different coagulation defects in a family.
PMID 11224586·Indian Pediatr·2001
5-case
Chorea: an unusual presenting feature in pediatric Moyamoya disease.
PMID 10992339·Indian Pediatr·2000
5-case
High resolution genotyping of Bacillus anthracis outbreak strains using four highly mutable single nucleotide repeat markers.
PMID 18363651·Lett Appl Microbiol·2008
7-preclinical
Chemistry of fogs at Agra, India: influence of soil particulates and atmospheric gases.
PMID 17294279·Environ Monit Assess·2007
8-other
Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome.
PMID 17357087·Am J Hum Genet·2007
8-other
Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
PMID 17846997·Am J Hum Genet·2007
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
- 2036 FOULK RD, SUITE #203
WILMINGTON, DE 19810 - Phone
- (302) 475-3403
Quick Facts
- NPI
- 1821221573
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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