Tóth T - Search Results

1

Phenotypic characterization of a DFNA6 family showing progressive low-frequency sensorineural hearing impairment.

Tóth T, Pfister M, Zenner HP, Sziklai I. Tóth T, et al. Int J Pediatr Otorhinolaryngol. 2006 Feb;70(2):201-6. doi: 10.1016/j.ijporl.2005.06.011. Epub 2005 Jul 25. Int J Pediatr Otorhinolaryngol. 2006. PMID: 16043233

2

Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairment.

Tóth T, Kupka S, Esmer H, Zeissler U, Sziklai I, Zenner HP, Blin N, Pfister M. Tóth T, et al. Int J Mol Med. 2001 Aug;8(2):189-92. Int J Mol Med. 2001. PMID: 11445873

3

[Phenotypic characterization of a DFNA6 family with low-frequency hearing loss].

Tóth T, Kupka S, Nürnberg P, Thiele H, Zenner HP, Sziklai I, Pfister M. Tóth T, et al. HNO. 2004 Feb;52(2):132-6. doi: 10.1007/s00106-003-0912-0. HNO. 2004. PMID: 14968315 German.

4

Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations.

Cryns K, Pfister M, Pennings RJ, Bom SJ, Flothmann K, Caethoven G, Kremer H, Schatteman I, Köln KA, Tóth T, Kupka S, Blin N, Nürnberg P, Thiele H, van de Heyning PH, Reardon W, Stephens D, Cremers CW, Smith RJ, Van Camp G. Cryns K, et al. Among authors: toth t. Hum Genet. 2002 May;110(5):389-94. doi: 10.1007/s00439-002-0719-1. Epub 2002 Apr 9. Hum Genet. 2002. PMID: 12073007

5

[Frequency of the Connexin26/35delG mutation and its characteristic phenotype in patients with hearing impairment and controls in Northeastern Hungary].

Tóth T, Kupka S, Blin N, Pfister M, Sziklai I. Tóth T, et al. Orv Hetil. 2002 Oct 6;143(40):2285-9. Orv Hetil. 2002. PMID: 12420583 Hungarian.

6

A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10.

Pfister M, Tóth T, Thiele H, Haack B, Blin N, Zenner HP, Sziklai I, Nürnberg P, Kupka S. Pfister M, et al. Among authors: toth t. Mol Med. 2002 Oct;8(10):607-11. Mol Med. 2002. PMID: 12477971 Free PMC article.

7

GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary.

Tóth T, Kupka S, Haack B, Riemann K, Braun S, Fazakas F, Zenner HP, Muszbek L, Blin N, Pfister M, Sziklai I. Tóth T, et al. Hum Mutat. 2004 Jun;23(6):631-2. doi: 10.1002/humu.9250. Hum Mutat. 2004. PMID: 15146474

8

Coincidence of mutations in different connexin genes in Hungarian patients.

Tóth T, Kupka S, Haack B, Fazakas F, Muszbek L, Blin N, Pfister M, Sziklai I. Tóth T, et al. Int J Mol Med. 2007 Sep;20(3):315-21. Int J Mol Med. 2007. PMID: 17671735

9

[The effects of auditory research on clinical practice].

Sziklai I, Tóth T, Zimmermann U. Sziklai I, et al. Among authors: toth t. HNO. 2003 Jun;51(6):456-61. doi: 10.1007/s00106-003-0851-9. Epub 2003 Apr 18. HNO. 2003. PMID: 12835843 Review. German.

10

[Phenotype of patients showing hearing impairment based on the 35delG mutation in the connexin 26 gene].

Tóth T, Kupka S, Sziklai I, Blin N, Zenner HP, Pfister M. Tóth T, et al. HNO. 2003 May;51(5):400-4. doi: 10.1007/s00106-002-0737-2. Epub 2003 Mar 27. HNO. 2003. PMID: 12835856 German.

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