Analysis of 223 cases of hereditary deafness
Zhuang, J.M.; Wang, D.X.
Zhonghua Yi Xue Za Zhi 66(1): 25-28
1986
ISSN/ISBN: 0376-2491 PMID: 3091213 Document Number: 283415
Document emailed within 1 workday
Related Documents
Gryczyńska, D.; Gryczyński, M. 1990: Problem of hereditary deafness Otolaryngologia Polska 44(4): 282-286Lu, S.M. 1981: Sex-linked recessive hereditary deafness Zhonghua Yi Xue Za Zhi 61(11): 666-667
Konigsmark, B.W. 1971: Syndromal approaches to the nosology of hereditary deafness Birth Defects Original Article Series 07(4): 2-17
Nuutila, A. 1972: A hereditary disease causing deafness and blindness Duodecim; Laaketieteellinen Aikakauskirja 88(1): 40-42
Zolezzi, P.; Faúndez; Norambuena, L.; Prieto, C. 1981: A hereditary mechanobullous diseases: histopathological clinical analysis of 2 cases Revista Chilena de Pediatria 52(1): 65-68
Moatti, L. 1983: Cases of rubella deafness Journal Francais d'Oto-Rhino-Laryngologie; Audiophonologie Chirurgie Maxillo-Faciale 32(5): 321-322
Lavy, J.A. 1998: Sudden onset deafness: two cases associated with pregnancy International Journal of Clinical Practice 52(2): 129-130
Fischer, C.; Joyeux, O.; Haguenauer, J.P.; Mauguière, F.; Schott, B. 1984: Deafness and tinnitus in flare-ups in 10 cases of multiple sclerosis Revue Neurologique (Paris) 140(2): 117-124
Fares, G.; Aïdan, P.; Bouccara, D.; Soubrane, P.; Rey, A.; Sterkers, O. 1996: Sudden deafness disclosing acoustic neuroma. Apropos of 16 cases Revue de Laryngologie - Otologie - Rhinologie 117(3): 167-170
García Callejo, F.J.; Sebastián Gil, E.; Morant Ventura, A.; Marco Algarra, J. 2002: Presentation of 2 cases of sudden deafness in patients with sickle-cell anemia and trait Acta Otorrinolaringologica Espanola 53(5): 371-376
Chabolle, F.; Garabedian, N.; Meyer, B.; Chouard, C.H. 1988: Results and therapeutic indications of the electrical stimulation of the round window in 581 cases of bilateral total deafness Annales d'Oto-Laryngologie et de Chirurgie Cervico Faciale: Bulletin de la Societe d'Oto-Laryngologie des Hopitaux de Paris 105(4): 237-241
Sterkers, J.M. 1980: Aplasia of the oval window and the fallopian aqueduct. Cure of deafness by an attico-vestibular piston (3 cases) Annales d'Oto-Laryngologie et de Chirurgie Cervico Faciale: Bulletin de la Societe d'Oto-Laryngologie des Hopitaux de Paris 97(7-8): 609-615
Ginter, E.K.; Budagova, K.A.; Revazov, A.A.; Petrin, A.N.; Bugaeva, E.A. 1986: Medico-genetical study of the Uzbekistan population. IX. Variability of hereditary pathology, territorial distribution of hereditary diseases and hereditary disease load in the population of the Urgut district of the Samarkand region Genetika 22(7): 1199-1206
Nie, M.; Liu, Y.; Wei, Y. 2015: Curative effects analysis of using HBOT combined with medicine to treat occupational noise deafness patients from rubber factory workers Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi 33(8): 622-623
Akimov, V.N. 1979: Cochlear analysis of sound intensity and various functional-morphological aspects of occupational vibration- and noise-induced hearing loss and deafness Vestnik Otorinolaringologii 6: 35-39
Szpringer, M.; Janicha, J. 1974: 2 cases of hereditary dentin dysplasia Czasopismo Stomatologiczne 27(4): 329-335
Stanghelle, J.K. 1980: Hereditary elliptocytosis. a family with 6 cases Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 100(32): 1911-1912
Rozier, J.C. 1971: Sporadic cases of hereditary spherocytosis North Carolina Medical Journal 32(4): 136-140
Kamei, T.; Noro, H.; Yabe, K.; Makino, S. 1971: Statistical observation of unilateral total deafness and characteristics of unilateral total deafness among young children with tendency toward dizziness Jibi Inkoka Otolaryngology 43(5): 349-358
Sudo, K.; Maekawa, M. 1999: Analysis of hereditary enzyme abnormalities Rinsho Byori. Japanese Journal of Clinical Pathology Suppl 109: 168-178