Tieri L - Search Results

1

Maternally inherited deafness associated with a T1095C mutation in the mDNA.

Tessa A, Giannotti A, Tieri L, Vilarinho L, Marotta G, Santorelli FM. Tessa A, et al. Among authors: tieri l. Eur J Hum Genet. 2001 Feb;9(2):147-9. doi: 10.1038/sj.ejhg.5200601. Eur J Hum Genet. 2001. PMID: 11313749

2

Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome).

Digilio MC, Pacifico C, Tieri L, Marino B, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: tieri l. Br J Audiol. 1999 Oct;33(5):329-33. doi: 10.3109/03005369909090116. Br J Audiol. 1999. PMID: 10890147

3

Rapid detection of the 35delG mutation in the GJB2 gene in childhood deafness.

Tessa A, Patrono C, Santorelli FM, Giannotti A, Digilio MC, Pacifico C, Presuttari F, Tieri L. Tessa A, et al. Among authors: tieri l. J Med Screen. 2000;7(3):167. doi: 10.1136/jms.7.3.167. J Med Screen. 2000. PMID: 11126168 No abstract available.

4

Nasal cartilage aplasia in a family with facioaudiosymphalangism syndrome.

Obregon MG, Digilio MC, Mingarelli R, Pacifico C, Tieri L, Giannotti A, Dallapiccola B. Obregon MG, et al. Among authors: tieri l. Am J Otolaryngol. 2000 Nov-Dec;21(6):405-8. doi: 10.1053/ajot.2000.18878. Am J Otolaryngol. 2000. PMID: 11115527 No abstract available.

5

Unilateral sensorineural hearing loss in children.

Tieri L, Masi R, Ducci M, Marsella P. Tieri L, et al. Scand Audiol Suppl. 1988;30:33-6. Scand Audiol Suppl. 1988. PMID: 3227281

6

Otologic impairments in achondroplasia: a nosologic assessment.

Pinelli V, Masi R, Partipilo P, Pierro V, Tieri L. Pinelli V, et al. Among authors: tieri l. Basic Life Sci. 1988;48:149-52. doi: 10.1007/978-1-4684-8712-1_20. Basic Life Sci. 1988. PMID: 3240244

7

Sensorineural hearing loss in patients reaching chronic renal failure in childhood.

Mancini ML, Dello Strologo L, Bianchi PM, Tieri L, Rizzoni G. Mancini ML, et al. Among authors: tieri l. Pediatr Nephrol. 1996 Feb;10(1):38-40. doi: 10.1007/BF00863438. Pediatr Nephrol. 1996. PMID: 8611353 Clinical Trial.

8

Bone-anchored hearing aid (Baha) in patients with Treacher Collins syndrome: tips and pitfalls.

Marsella P, Scorpecci A, Pacifico C, Tieri L. Marsella P, et al. Among authors: tieri l. Int J Pediatr Otorhinolaryngol. 2011 Oct;75(10):1308-12. doi: 10.1016/j.ijporl.2011.07.020. Epub 2011 Aug 11. Int J Pediatr Otorhinolaryngol. 2011. PMID: 21839526

9

[Unilateral sensorineural deafness in childhood].

Tieri L, Masi R, Ducci M, Marsella P. Tieri L, et al. Acta Otorhinolaryngol Ital. 1988;8 Suppl 19:99-106. Acta Otorhinolaryngol Ital. 1988. PMID: 3213505 Italian. No abstract available.

10

Sudden deafness in children.

Tieri L, Masi R, Marsella P, Pinelli V. Tieri L, et al. Int J Pediatr Otorhinolaryngol. 1984 Jul;7(3):257-64. doi: 10.1016/s0165-5876(84)80006-3. Int J Pediatr Otorhinolaryngol. 1984. PMID: 6480234

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