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

Year Number of Results
1997 3
1998 1
1999 1
2001 1
2002 2
2003 2
2004 1
2005 5
2006 2
2007 2
2008 2
2009 2
2010 3
2011 3
2012 5
2013 7
2014 5
2015 4
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82 results

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Page 1
HASHIMOTO THYROIDITIS AND VESTIBULAR DYSFUNCTION.
Chiarella G, Russo D, Monzani F, Petrolo C, Fattori B, Pasqualetti G, Cassandro E, Costante G. Chiarella G, et al. Endocr Pract. 2017 Jul;23(7):863-868. doi: 10.4158/EP161635.RA. Epub 2017 May 23. Endocr Pract. 2017. PMID: 28534686 Review.
ABBREVIATIONS: AITD = autoimmune thyroid disease; BPPV = benign paroxysmal positional vertigo; EH = endolymphatic hydrops; HT = Hashimoto thyroiditis; L-T(4) = L-thyroxine; MD = Meniere disease; PS = Pendred syndrome; Tg = thyroglobulin; TPO = thyroid peroxidase; TS …
ABBREVIATIONS: AITD = autoimmune thyroid disease; BPPV = benign paroxysmal positional vertigo; EH = endolymphatic hydrops; HT = Hashimoto th …
Hereditary and familial thyroid tumours.
Guilmette J, Nosé V. Guilmette J, et al. Histopathology. 2018 Jan;72(1):70-81. doi: 10.1111/his.13373. Histopathology. 2018. PMID: 29239041 Review.
Among the first group are found syndromes characterised by a predominance of non-thyroidal tumours, including familial adenomatous polyposis, Cowden syndrome, Werner syndrome, Carney complex, and Pendred syndrome. The second group encompasses a spectrum of familial …
Among the first group are found syndromes characterised by a predominance of non-thyroidal tumours, including familial adenomatous polyposis …
Cochlear implantation in patients with Pendred syndrome.
Patterson TE, Gonzalez VB, Carron JD. Patterson TE, et al. Am J Otolaryngol. 2021 Nov-Dec;42(6):103087. doi: 10.1016/j.amjoto.2021.103087. Epub 2021 May 19. Am J Otolaryngol. 2021. PMID: 34029917
OBJECTIVE: To examine the outcomes of cochlear implantation in children with Pendred Syndrome. MATERIAL AND METHODS: A retrospective case series of nine pediatric patients with Pendred syndrome undergoing cochlear implantation at a tertiary academic me …
OBJECTIVE: To examine the outcomes of cochlear implantation in children with Pendred Syndrome. MATERIAL AND METHODS: A retrosp …
Speech Perception and Production in Cochlear Implant Recipients with Pendred Syndrome.
Skrivan J, Jurovcik M, Aksenovova Z, Astl J, Pourova RK, Dytrych P, Sieger T. Skrivan J, et al. Balkan Med J. 2021 Jul;38(4):244-248. doi: 10.5152/balkanmedj.2021.20182. Balkan Med J. 2021. PMID: 34274914 Free PMC article.
In the study, we compared speech production and speech acquisition in 2 groups of implanted patients: those with the Pendred syndrome, and standard non-syndromic patients. METHODS: Ten patients with Pendred syndrome were analyzed for speech perception …
In the study, we compared speech production and speech acquisition in 2 groups of implanted patients: those with the Pendred syndr …
Vestibular Function in Pendred Syndrome: Intact High Frequency VOR and Saccular Hypersensitivity.
West NC, Ryberg AC, Cayé-Thomasen P. West NC, et al. Otol Neurotol. 2021 Oct 1;42(9):e1327-e1332. doi: 10.1097/MAO.0000000000003270. Otol Neurotol. 2021. PMID: 34224544
OBJECTIVE: Although Pendred syndrome involves anatomical abnormalities in the vestibular system and patient-perceived dizziness, the literature on vestibular function is scarce. ...CONCLUSION: Despite dysmorphic vestibular anatomy and severe loss of hearing, the VHI …
OBJECTIVE: Although Pendred syndrome involves anatomical abnormalities in the vestibular system and patient-perceived dizzines …
Molecular genetic landscape of hereditary hearing loss in Pakistan.
Naz S. Naz S. Hum Genet. 2022 Apr;141(3-4):633-648. doi: 10.1007/s00439-021-02320-0. Epub 2021 Jul 25. Hum Genet. 2022. PMID: 34308486 Review.
Though significant progress has been made in uncovering genetic variants for recessively inherited nonsyndromic deafness, Pendred syndrome, and Usher syndromes, the same is not true for dominantly inherited hearing loss, most syndromic cases and deafness with comple …
Though significant progress has been made in uncovering genetic variants for recessively inherited nonsyndromic deafness, Pendred …
Association of SLC26A4 mutations, morphology, and hearing in pendred syndrome and NSEVA.
Mey K, Muhamad AA, Tranebjaerg L, Rendtorff ND, Rasmussen SH, Bille M, Cayé-Thomasen P. Mey K, et al. Laryngoscope. 2019 Nov;129(11):2574-2579. doi: 10.1002/lary.27319. Laryngoscope. 2019. PMID: 31633822
OBJECTIVE: To investigate the relations of monoallelic (M1), biallelic (M2), or the absence of mutations (M0) in SLC26A4 to inner ear morphology and hearing levels in individuals with Pendred syndrome (PS) or nonsyndromic enlarged vestibular aqueduct (NSEVA) associa …
OBJECTIVE: To investigate the relations of monoallelic (M1), biallelic (M2), or the absence of mutations (M0) in SLC26A4 to inner ear morpho …
Genetics of congenital hypothyroidism.
Park SM, Chatterjee VK. Park SM, et al. J Med Genet. 2005 May;42(5):379-89. doi: 10.1136/jmg.2004.024158. J Med Genet. 2005. PMID: 15863666 Free PMC article. Review.
Among those causing dyshormonogenesis, the thyroid peroxidase and thyroglobulin genes were initially described, and more recently PDS (Pendred syndrome), NIS (sodium iodide symporter), and THOX2 (thyroid oxidase 2) gene defects. ...
Among those causing dyshormonogenesis, the thyroid peroxidase and thyroglobulin genes were initially described, and more recently PDS (Pe …
Molecular and functional characterization of human pendrin and its allelic variants.
Dossena S, Nofziger C, Tamma G, Bernardinelli E, Vanoni S, Nowak C, Grabmayer E, Kössler S, Stephan S, Patsch W, Paulmichl M. Dossena S, et al. Cell Physiol Biochem. 2011;28(3):451-66. doi: 10.1159/000335107. Epub 2011 Nov 18. Cell Physiol Biochem. 2011. PMID: 22116358 Free article. Review.
Functional tests of mutated pendrin allelic variants found in patients with Pendred syndrome or non-syndromic EVA (ns-EVA) revealed that the pathological phenotype is due to the reduction or loss of function of the ion transport activity. The diagnosis of Pendred …
Functional tests of mutated pendrin allelic variants found in patients with Pendred syndrome or non-syndromic EVA (ns-EVA) rev …
Thyroid cancer of follicular cell origin in inherited tumor syndromes.
Nosé V. Nosé V. Adv Anat Pathol. 2010 Nov;17(6):428-36. doi: 10.1097/PAP.0b013e3181f8b028. Adv Anat Pathol. 2010. PMID: 20966648 Review.
The first group, syndromic-associated tumors, includes phosphase and tensin (PTEN)-hamartoma tumor syndrome/Cowden syndrome, familial adenomatous polyposis/Gardner syndrome, Carney complex type 1, Werner syndrome, and Pendred syndrome. Other syndromes, as McCune Alb …
The first group, syndromic-associated tumors, includes phosphase and tensin (PTEN)-hamartoma tumor syndrome/Cowden syndrome, familial adenom …
82 results