L. Tieri

Maternally inherited deafness associated with a T1095C mutation in the mDNA

Alessandra Tessa, Aldo Giannotti, L. Tieri et al. · European Journal of Human Genetics · 2001 · 67 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +11

Audiological Findings in Patients with Microdeletion 22Qll (Di George/Velocardiofacial Syndrome)

M. Cristina Digilio, Concettina Pacifico, L. Tieri et al. · British Journal of Audiology · 1999 · 62 citations

Heart Failure, Genetic Syndromes, Microdeletion 22Qll +17

Sensorineural hearing loss in patients reaching chronic renal failure in childhood

Mario Mancini, Luca Dello Strologo, P Bianchi et al. · Pediatric Nephrology · 1996 · 60 citations

Early Diagnosis, Sensorineural Hearing Loss, Chronic Renal Failure +11

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

Pasquale Marsella, Alessandro Scorpecci, Concettina Pacifico et al. · International Journal of Pediatric Otorhinolaryngology · 2011 · 43 citations

Treacher Collins Syndrome, Pediatric Otolaryngology, Audiology +7

Sudden deafness in children

L. Tieri, Roberto De Masi, Pasquale Marsella et al. · International Journal of Pediatric Otorhinolaryngology · 1984 · 15 citations

Pediatric Otolaryngology, Audiology, Language Development +7