Ali Attaie, DDS
- ASSISTANT CLINICAL PROFESSOR | Dentistry
- ASSISTANT CLINICAL PROFESSOR | Pediatrics
Clinical foci include: early childhood caries, pediatric sedation and management, pain management, pediatric dentofacial trauma, pediatric hospital dentistry and dental surgery, cleft lip and palate, ectodermal dysplasia, pediatric obstructive sleep apnea, interceptive orthodontics, school based oral health, dental treatment of children with developmental delay and special needs, pediatric oral health in medical education and workforce and access to care for pediatric oral health.
Residency, Dentistry Pediatric, Lutheran Medical Center
Burow L, Attaie AB. Changing How We Care: Innovating the Dental Care Experience for Underserved Communities in New York City. Touchpoint: The Journal of Service Design 2012 January; 3(3).
Attaie A. Access to care: unresolved challenges and call for solutions. Mouth: Journal of the American Student Dental Association 2002;(Winter): 28.
Bikhazi PH, Roeder E, Attaie A, Lalwani AK. Familial paragangliomas: the emerging impact of molecular genetics on evaluation and management. American Journal of Otology 1999 September;: 639-643.
Lalwani AK, Luxford WM, Mhatre AN, Attaie A, Wilcox ER, Castelein CM. A new locus for nonsyndromic hereditary hearing impariment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration [letter]. American Journal of Human Genetics 1999 January;: 318-323.
Lalwani AK, Attaie A, Randolph FT, Deshmukh D, Wang C, Mhatre A, Wilcox E. Point mutation in the MITF gene causing Waardenburg syndrome type II in a three-generation Indian family. American Journal of Medical Genetics 1998 December;: 406-409.
Attaie A, Kim E, Wilcox ER, Lalwani AK. A splice-site mutation affecting the paired box of PAX3 in a three generation family with Waardenburg syndrome type 1. Molecular and Cellular Probes 1997 June;: 233-236.
Wang C, Kim E, Attaie A, Smith TN, Wilcox ER, Lalwani AK. A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome type 2. Molecular and Cellular Probes 1998 February;: 55-57.
A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration. Audiology and Neuro-Otology 1997 May-June;: 139-154.