Search Results - "Attaie, Ali"

Genetic Basis of Nonsyndromic and Syndromic Tooth Agenesis by Ye, Xiaoqian, Attaie, Ali B

“…Human dentition development is a long and complex process which involves a series of reciprocal and sequential interactions between the embryonic stomodeal…”
Get full text

Use of the Hall technique by specialist paediatric dentists: a global perspective by Hussein, Iyad, Al Halabi, Manal, Kowash, Mawlood, Salami, Anas, Ouatik, Nabil, Yang, Yeon-Mi, Duggal, Monty, Chandwani, Neeta, Nazzal, Hani, Albadri, Sondos, Roberts, Amanda, Al-Jundi, Suhad, Nzomiwu, Chioma, El Shahawy, Osama, Attaie, Ali, Mohammed, Ossama, Al-Sane, Mona

“…Background The Hall technique (HT) is popular with UK paediatric dentists (PDs). Global PDs perception/use of HT is unknown. Aim To investigate global PDs…”
Get full text

Novel mutations in EVC cause aberrant splicing in Ellis–van Creveld syndrome by Shi, Lisong, Luo, Chunyan, Ahmed, Mairaj K., Attaie, Ali B., Ye, Xiaoqian

“…Ellis–van Creveld syndrome (EvC) is a rare autosomal recessive disorder characterized by disproportionate chondrodysplasia, postaxial polydactyly, nail…”
Get full text

A New Locus for Nonsyndromic Hereditary Hearing Impairment, DFNA17, Maps to Chromosome 22 and Represents a Gene for Cochleosaccular Degeneration by Lalwani, Anil K., Luxford, William M., Mhatre, Anand N., Attaie, Ali, Wilcox, Edward R., Castelein, Caley M.

Get full text

Esthetics and pediatric dentistry by Attaie, Ali B, Ouatik, Nabil

Get full text

19 - Esthetics and pediatric dentistry by Attaie, Ali B., Ouatik, Nabil

Get full text

Germline Screening of the NF-2 Gene in Families with Unilateral Vestibular Schwannoma by Bikhazi, Paul H., Kim, Eugene J., Attaie, Ali, Bikhazi, Nadim B., Lalwani, Anil K.

Get full text

Familial paragangliomas : The emerging impact of molecular genetics on evaluation and management by BIKHAZI, P. H, ROEDER, E, ATTAIE, A, LALWANI, A. K

“…Advancements in molecular genetics has direct impact on the evaluation and management of patients and family members with familial paragangliomas (FP)…”
Get full text

First Place—Resident Clinical Science Award 1997: Germline screening of the NF-2 gene in families with unilateral vestibular schwannoma by Bikhazi, Paul H., Lalwani, Anil K., Kim, Eugene J., Bikhazi, Nadim, Attaie, Ali, Slattery, William H., Jackler, Robert K., Brackmann, Derald E.

“…Vestibular schwannoma may present clinically in two forms: sporadic unilateral or hereditary bilateral. Familial transmission of vestibular schwannoma is known…”
Get full text

A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration by Lalwani, A K, Linthicum, F H, Wilcox, E R, Moore, J K, Walters, F C, San Agustin, T B, Mislinski, J, Miller, M R, Sinninger, Y, Attaie, A, Luxford, W M

“…Cochleosaccular dysplasia or degeneration (Scheibe degeneration) is considered the most common cause of profound congenital hearing impairment, and accounts…”
Get more information

Germline screening of the NF-2 gene in families with unilateral vestibular schwannoma by Bikhazi, Paul H., Kim, Eugene J., Attaie, Ali, Bikhazi, Nadim B., Lalwani, Anil K.

Get full text

A splice-site mutation affecting the paired box of PAX3 in a three generation family with Waardenburg syndrome type I (WS1) by Attaie, Ali, Kim, Eugene, Wilcox, Edward R., Lalwani, Anil K.

“…Waardenburg syndrome, an autosomal dominant disorder characterized by sensorineural hearing loss, pigmentary disturbances and other developmental defects, is…”
Get full text

Germline screening of the NF-2 gene in families with unilateral vestibular schwannoma by BIKHAZI, PAUL H., LALWANI, ANIL K., KIM, EUGENE J., BIKHAZI, NADIM, ATTAIE, ALI, SLATTERY, WILLIAM H., JACKLER, ROBERT K., BRACKMANN, DERALD E.

“…Vestibular schwannoma may present clinically in two forms: sporadic unilateral or hereditary bilateral. Familial transmission of vestibular schwannoma is known…”
Get full text

A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome Type 2 (WS2) by Wang, Cynthia, Kim, Eugene, Attaie, Ali, Smith, Tenesha N, Wilcox, Edward R, Lalwani, Anil K

“…Waardenburg Syndrome (WS) is an autosomal-dominant disorder phenotypically characterized by sensorineural hearing loss and pigmentary disturbances. Presence of…”
Get full text

Point mutation in the MITF gene causing Waardenburg syndrome type II in a three-generation Indian family by Lalwani, Anil K., Attaie, Ali, Randolph, Frederick T., Deshmukh, Dilip, Wang, Cynthia, Mhatre, Anand, Wilcox, Edward

“…Waardenburg syndrome (WS) is an autosomal‐dominant neural crest cell disorder phenotypically characterized by hearing impairment and disturbance of…”
Get full text