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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1962 2
1963 3
1964 1
1965 1
1966 3
1967 2
1969 1
1971 1
1980 1
1981 2
1982 1
1983 1
1986 2
1988 1
1992 1
1993 1
1996 3
1997 5
1998 12
1999 11
2000 11
2001 11
2002 14
2003 14
2004 10
2005 14
2006 19
2007 16
2008 19
2009 15
2010 18
2011 29
2012 22
2013 22
2014 19
2015 9
2016 18
2017 17
2018 10
2019 19
2020 21
2021 19
2022 21
2023 16
2024 7

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413 results

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Page 1
Pendred syndrome.
Wémeau JL, Kopp P. Wémeau JL, et al. Best Pract Res Clin Endocrinol Metab. 2017 Mar;31(2):213-224. doi: 10.1016/j.beem.2017.04.011. Epub 2017 May 10. Best Pract Res Clin Endocrinol Metab. 2017. PMID: 28648509 Review.
Pendred syndrome is an autosomal recessive disorder that is classically defined by the combination of sensorineural deafness/hearing impairment, goiter, and an abnormal organification of iodide with or without hypothyroidism. ...While there is no renal phenotype und …
Pendred syndrome is an autosomal recessive disorder that is classically defined by the combination of sensorineural deafness/h …
Pendred Syndrome.
Garabet Diramerian L, Ejaz S. Garabet Diramerian L, et al. 2023 Apr 24. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Apr 24. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 31751029 Free Books & Documents.
Pendred syndrome characteristically presents with a combination of sensorineural hearing loss and thyroid goiter with or without hypothyroidism. ...
Pendred syndrome characteristically presents with a combination of sensorineural hearing loss and thyroid goiter with or witho …
Pendred Syndrome / Nonsyndromic Enlarged Vestibular Aqueduct.
Smith RJH, Iwasa Y, Schaefer AM. Smith RJH, et al. 1998 Sep 28 [updated 2020 Jun 18]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 1998 Sep 28 [updated 2020 Jun 18]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301640 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Pendred syndrome / nonsyndromic enlarged vestibular aqueduct (PDS/NSEVA) comprises a phenotypic spectrum of sensorineural hearing loss (SNHL) that is usually congenital and often severe to profound (although mild-to-moderate progressive hea …
CLINICAL CHARACTERISTICS: Pendred syndrome / nonsyndromic enlarged vestibular aqueduct (PDS/NSEVA) comprises a phenotypic spec …
Pendred syndrome.
Glaser B. Glaser B. Pediatr Endocrinol Rev. 2003 Dec;1 Suppl 2:199-204; discussion 204. Pediatr Endocrinol Rev. 2003. PMID: 16444159 Review.
Pendred Syndrome, first described in 1896, is phenotypically characterized as the coexistence of sensorineural deafness and enlarged goiter with elevated iodine discharge after perchlorate administration. ...The pathophysiology of the hearing loss associated with …
Pendred Syndrome, first described in 1896, is phenotypically characterized as the coexistence of sensorineural deafness and en …
Pendred syndrome with hyperthyroidism.
Kusano Y. Kusano Y. J Rural Med. 2020 Oct;15(4):217-220. doi: 10.2185/jrm.2020-011. Epub 2020 Oct 1. J Rural Med. 2020. PMID: 33033545 Free PMC article.
Objectives: Pendred syndrome is an autosomal recessive disorder characterized by the combination of sensorineural deafness and goiter and is caused by biallelic mutations in the SLC26A4/PDS gene. ...Results: She had a homozygous mutation in c.1579A>C:p.T527P of t …
Objectives: Pendred syndrome is an autosomal recessive disorder characterized by the combination of sensorineural deafness and …
Pendred syndrome.
Reardon W, Trembath RC. Reardon W, et al. J Med Genet. 1996 Dec;33(12):1037-40. doi: 10.1136/jmg.33.12.1037. J Med Genet. 1996. PMID: 9004139 Free PMC article. Review. No abstract available.
Pendred Syndrome, or Not Pendred Syndrome? That Is the Question.
Tesolin P, Fiorino S, Lenarduzzi S, Rubinato E, Cattaruzzi E, Ammar L, Castro V, Orzan E, Granata C, Dell'Orco D, Morgan A, Girotto G. Tesolin P, et al. Genes (Basel). 2021 Oct 1;12(10):1569. doi: 10.3390/genes12101569. Genes (Basel). 2021. PMID: 34680964 Free PMC article.
Pendred syndrome (PDS) is the most common form of syndromic Hearing Loss (HL), characterized by sensorineural HL, inner ear malformations, and goiter, with or without hypothyroidism. ...
Pendred syndrome (PDS) is the most common form of syndromic Hearing Loss (HL), characterized by sensorineural HL, inner ear ma …
Pendred syndrome.
Lado Abeal J. Lado Abeal J. Expert Rev Endocrinol Metab. 2008 Sep;3(5):635-643. doi: 10.1586/17446651.3.5.635. Expert Rev Endocrinol Metab. 2008. PMID: 30290408
Pendred syndrome (PDS) is an autosomal recessive disorder clinically characterized by sensorineural hearing loss and goiter. ...
Pendred syndrome (PDS) is an autosomal recessive disorder clinically characterized by sensorineural hearing loss and goiter. . …
[Pendred syndrome].
Suzuki K, Yoshida A, Fukata S. Suzuki K, et al. Nihon Rinsho. 2006 May 28;Suppl 1:371-3. Nihon Rinsho. 2006. PMID: 16776168 Review. Japanese. No abstract available.
Pendred syndrome and iodide transport in the thyroid.
Kopp P, Pesce L, Solis-S JC. Kopp P, et al. Trends Endocrinol Metab. 2008 Sep;19(7):260-8. doi: 10.1016/j.tem.2008.07.001. Epub 2008 Aug 7. Trends Endocrinol Metab. 2008. PMID: 18692402 Review.
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural hearing impairment, presence of goiter, and a partial defect in iodide organification, which may be associated with insufficient thyroid hormone synthesis. Goiter development and deve …
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural hearing impairment, presence of goiter, and …
413 results