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By Braun Jean Jacques   Pauli Gabrielle   Schultz Philippe   Gentine André   Ebbo David   de Blay Frédéric  

American Journal of Rhinology, Vol. 21, Iss. 4, 2007-07 ,pp. : 412-416

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Phenotypic consequences in a Japanese family having branchio-oto-renal syndrome with a novel frameshift mutation in the gene EYA1

By Matsunaga Tatsuo   Okada Michiyo   Usami Shin-Ichi   Okuyama Torayuki  

Acta Oto-Laryngologica, Vol. 127, Iss. 1, 2007-01 ,pp. : 98-104

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A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss

By Noguchi Yoshihiro   Yashima Takatoshi   Hatanaka Akio   Uzawa Masamichi   Yasunami Michio   Kimura Akinori   Kitamura Ken  

Acta Oto-Laryngologica, Vol. 125, Iss. 11, 2005-11 ,pp. : 1189-1194

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Communication aids for people with aphasia

By Kitzing Peter   Ahlsén Elisabeth   Jönsson Bodil  

Logopedics Phoniatrics Vocology, Vol. 30, Iss. 1, 2005-06 ,pp. : 41-46

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Cogan's syndrome: a case report

By Klement Vladislav   Hahn Ales   Hojdarova Alena   Sejna Ivan  

Acta Oto-Laryngologica, Vol. 127, Iss. 10, 2007-01 ,pp. : 1115-1117

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