BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

277 related articles for article (PubMed ID: 19235486)

  • 21. Pendred Syndrome in a Newborn with Neck Swelling: A Case Report.
    Ajij M; Shambhavi ; Patra B; Singh A; Kapoor S
    J Trop Pediatr; 2016 Aug; 62(4):338-40. PubMed ID: 26936928
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders].
    Mironovich OL; Bliznetz EA; Markova TG; Geptner EN; Lalayants MR; Zelikovich EI; Tavartkiladze GA; Polyakov AV
    Genetika; 2017 Jan; 53(1):88-99. PubMed ID: 29372807
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular analysis of the PDS gene in Pendred syndrome.
    Coyle B; Reardon W; Herbrick JA; Tsui LC; Gausden E; Lee J; Coffey R; Grueters A; Grossman4 A; Phelps PD; Luxon L; Kendall-Taylor P; Scherer SW; Trembath RC
    Hum Mol Genet; 1998 Jul; 7(7):1105-12. PubMed ID: 9618167
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Pendred syndrome and iodide transport in the thyroid.
    Kopp P; Pesce L; Solis-S JC
    Trends Endocrinol Metab; 2008 Sep; 19(7):260-8. PubMed ID: 18692402
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical and molecular characteristics of Pendred syndrome.
    Kopp P; Bizhanova A
    Ann Endocrinol (Paris); 2011 Apr; 72(2):88-94. PubMed ID: 21511235
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing loss.
    Cama E; Alemanno MS; Bellacchio E; Santarelli R; Carella M; Zelante L; Palladino T; Inches I; di Paola F; Arslan E; Melchionda S
    Int J Pediatr Otorhinolaryngol; 2009 Oct; 73(10):1458-63. PubMed ID: 19615760
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular analysis of the PDS gene in a nonconsanguineous Sicilian family with Pendred's syndrome.
    Gillam MP; Bartolone L; Kopp P; Benvenga S
    Thyroid; 2005 Jul; 15(7):734-41. PubMed ID: 16053392
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.
    Kühnen P; Turan S; Fröhler S; Güran T; Abali S; Biebermann H; Bereket A; Grüters A; Chen W; Krude H
    J Clin Endocrinol Metab; 2014 Jan; 99(1):E169-76. PubMed ID: 24248179
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4).
    Scott DA; Wang R; Kreman TM; Andrews M; McDonald JM; Bishop JR; Smith RJ; Karniski LP; Sheffield VC
    Hum Mol Genet; 2000 Jul; 9(11):1709-15. PubMed ID: 10861298
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: identification of two novel mutations in Brazilian patients.
    de Moraes VC; dos Santos NZ; Ramos PZ; Svidnicki MC; Castilho AM; Sartorato EL
    Int J Pediatr Otorhinolaryngol; 2013 Mar; 77(3):410-3. PubMed ID: 23273637
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hereditary hearing loss with thyroid abnormalities.
    Choi BY; Muskett J; King KA; Zalewski CK; Shawker T; Reynolds JC; Butman JA; Brewer CC; Stewart AK; Alper SL; Griffith AJ
    Adv Otorhinolaryngol; 2011; 70():43-49. PubMed ID: 21358184
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of a founder mutation for Pendred syndrome in families from northwest Iran.
    Mohseni M; Honarpour A; Mozafari R; Davarnia B; Najmabadi H; Kahrizi K
    Int J Pediatr Otorhinolaryngol; 2014 Nov; 78(11):1828-32. PubMed ID: 25239229
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet.
    Calebiro D; Porazzi P; Bonomi M; Lisi S; Grindati A; De Nittis D; Fugazzola L; Marinò M; Bottà G; Persani L
    J Endocrinol Invest; 2011 Sep; 34(8):593-8. PubMed ID: 20834201
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical and molecular analysis of three Mexican families with Pendred's syndrome.
    Gonzalez Trevino O; Karamanoglu Arseven O; Ceballos CJ; Vives VI; Ramirez RC; Gomez VV; Medeiros-Neto G; Kopp P
    Eur J Endocrinol; 2001 Jun; 144(6):585-93. PubMed ID: 11375792
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome.
    Sagong B; Seok JH; Kwon TJ; Kim UK; Lee SH; Lee KY
    Gene; 2012 Oct; 508(1):135-9. PubMed ID: 22884721
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Two common and three novel PDS mutations in Thai patients with Pendred syndrome.
    Snabboon T; Plengpanich W; Saengpanich S; Sirisalipoch S; Keelawat S; Sunthornyothin S; Khovidhunkit W; Suwanwalaikorn S; Sridama V; Shotelersuk V
    J Endocrinol Invest; 2007 Dec; 30(11):907-13. PubMed ID: 18250610
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Phenotypes associated with replacement of His by Arg in the Pendred syndrome gene.
    Sato E; Nakashima T; Miura Y; Furuhashi A; Nakayama A; Mori N; Murakami H; Naganawa S; Tadokoro M
    Eur J Endocrinol; 2001 Dec; 145(6):697-703. PubMed ID: 11720893
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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
    Genes (Basel); 2021 Oct; 12(10):. PubMed ID: 34680964
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Solitary thyroid nodule as presenting symptom of Pendred syndrome caused by a novel splice-site mutation in intron 8 of the SLC26A4 gene.
    Massa G; Jaenen N; de Varebeke SJ; Peeters N; Wuyts W
    Eur J Pediatr; 2003 Oct; 162(10):674-7. PubMed ID: 12920581
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Novel heterozygous mutation c.662_663insG compound with IVS7-2A>G mutation in SLC26A4 gene in a Chinese family with Pendred syndrome.
    Chen K; Zhou W; Zong L; Liu M; Du J; Jiang H
    Int J Pediatr Otorhinolaryngol; 2012 Nov; 76(11):1633-6. PubMed ID: 22906308
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.