Similar articles for PMID: 15355436

Year	Number of Results
1953	1
1961	1
1962	2
1963	2
1964	1
1965	2
1966	9
1967	5
1968	4
1969	6
1970	4
1971	2
1972	3
1973	4
1974	2
1975	2
1977	6
1978	2
1980	2
1981	1
1982	1
1984	1
1986	2
1987	3
1989	3
1993	4
1994	2
1995	1
1996	2
1997	1
1998	3
1999	4
2000	7
2001	10
2002	3
2003	5
2004	6
2005	8
2006	8
2007	7
2008	6
2009	5
2010	3
2013	2
2022	1
2023	1
2024	0

1

Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.

Blons H, Feldmann D, Duval V, Messaz O, Denoyelle F, Loundon N, Sergout-Allaoui A, Houang M, Duriez F, Lacombe D, Delobel B, Leman J, Catros H, Journel H, Drouin-Garraud V, Obstoy MF, Toutain A, Oden S, Toublanc JE, Couderc R, Petit C, Garabédian EN, Marlin S. Blons H, et al. Clin Genet. 2004 Oct;66(4):333-40. doi: 10.1111/j.1399-0004.2004.00296.x. Clin Genet. 2004. PMID: 15355436

2

Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or Pendred syndrome.

Wu CC, Lu YC, Chen PJ, Yeh PL, Su YN, Hwu WL, Hsu CJ. Wu CC, et al. Audiol Neurootol. 2010;15(1):57-66. doi: 10.1159/000231567. Epub 2009 Aug 1. Audiol Neurootol. 2010. PMID: 19648736

3

Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene.

Kopp P, Arseven OK, Sabacan L, Kotlar T, Dupuis J, Cavaliere H, Santos CL, Jameson JL, Medeiros-Neto G. Kopp P, et al. J Clin Endocrinol Metab. 1999 Jan;84(1):336-41. doi: 10.1210/jcem.84.1.5398. J Clin Endocrinol Metab. 1999. PMID: 9920104

4

Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese.

Tsukamoto K, Suzuki H, Harada D, Namba A, Abe S, Usami S. Tsukamoto K, et al. Eur J Hum Genet. 2003 Dec;11(12):916-22. doi: 10.1038/sj.ejhg.5201073. Eur J Hum Genet. 2003. PMID: 14508505

5

Molecular analysis of the PDS gene in a nonconsanguineous Sicilian family with Pendred's syndrome.

Gillam MP, Bartolone L, Kopp P, Benvenga S. Gillam MP, et al. Thyroid. 2005 Jul;15(7):734-41. doi: 10.1089/thy.2005.734. Thyroid. 2005. PMID: 16053392

6

Molecular analysis of the Pendred's syndrome gene and magnetic resonance imaging studies of the inner ear are essential for the diagnosis of true Pendred's syndrome.

Fugazzola L, Mannavola D, Cerutti N, Maghnie M, Pagella F, Bianchi P, Weber G, Persani L, Beck-Peccoz P. Fugazzola L, et al. J Clin Endocrinol Metab. 2000 Jul;85(7):2469-75. doi: 10.1210/jcem.85.7.6694. J Clin Endocrinol Metab. 2000. PMID: 10902795 Clinical Trial.

7

SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.

Albert S, Blons H, Jonard L, Feldmann D, Chauvin P, Loundon N, Sergent-Allaoui A, Houang M, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Dollfus H, Eliot MM, David A, Calais C, Drouin-Garraud V, Obstoy MF, Tran Ba Huy P, Lacombe D, Duriez F, Francannet C, Bitoun P, Petit C, Garabédian EN, Couderc R, Marlin S, Denoyelle F. Albert S, et al. Eur J Hum Genet. 2006 Jun;14(6):773-9. doi: 10.1038/sj.ejhg.5201611. Eur J Hum Genet. 2006. PMID: 16570074

8

The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct.

Madden C, Halsted M, Meinzen-Derr J, Bardo D, Boston M, Arjmand E, Nishimura C, Yang T, Benton C, Das V, Smith R, Choo D, Greinwald J. Madden C, et al. Arch Otolaryngol Head Neck Surg. 2007 Feb;133(2):162-8. doi: 10.1001/archotol.133.2.162. Arch Otolaryngol Head Neck Surg. 2007. PMID: 17309986

9

Large vestibular aqueduct syndrome: audiological, radiological, clinical, and genetic features.

Berrettini S, Forli F, Bogazzi F, Neri E, Salvatori L, Casani AP, Franceschini SS. Berrettini S, et al. Am J Otolaryngol. 2005 Nov-Dec;26(6):363-71. doi: 10.1016/j.amjoto.2005.02.013. Am J Otolaryngol. 2005. PMID: 16275403

10

Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations.

Campbell C, Cucci RA, Prasad S, Green GE, Edeal JB, Galer CE, Karniski LP, Sheffield VC, Smith RJ. Campbell C, et al. Hum Mutat. 2001 May;17(5):403-11. doi: 10.1002/humu.1116. Hum Mutat. 2001. PMID: 11317356

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

156 results

Results by year