These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

91 related articles for article (PubMed ID: 18349467)

  • 1. Goitre and hearing impairment in a patient with Pendred syndrome.
    Arwert LI; Sepers JM
    Neth J Med; 2008 Mar; 66(3):118-20. PubMed ID: 18349467
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pendred syndrome.
    Glaser B
    Pediatr Endocrinol Rev; 2003 Dec; 1 Suppl 2():199-204; discussion 204. PubMed ID: 16444159
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndrome.
    Cremers WR; Bolder C; Admiraal RJ; Everett LA; Joosten FB; van Hauwe P; Green ED; Otten BJ
    Arch Otolaryngol Head Neck Surg; 1998 May; 124(5):501-5. PubMed ID: 9604973
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Phenotypic evaluation of patients with Pendred syndrome].
    Maciaszczyk K; Pniewska-Siark B; Gajewicz W; Stefańczyk L; Durko T; Lewiński A; Pajor A
    Otolaryngol Pol; 2008; 62(6):740-6. PubMed ID: 19205523
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Iodide perchlorate discharge test in lithium-treated patients.
    Andersen BF
    Acta Endocrinol (Copenh); 1973 May; 73(1):35-42. PubMed ID: 4350678
    [No Abstract]   [Full Text] [Related]  

  • 7. Genetics and phenomics of Pendred syndrome.
    Bizhanova A; Kopp P
    Mol Cell Endocrinol; 2010 Jun; 322(1-2):83-90. PubMed ID: 20298745
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome.
    Taylor JP; Metcalfe RA; Watson PF; Weetman AP; Trembath RC
    J Clin Endocrinol Metab; 2002 Apr; 87(4):1778-84. PubMed ID: 11932316
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [The diagnosis of the Pendred syndrome in children by the perchlorate discharge test with 123I (author's transl)].
    Gross M; Hahn K; Biesalski HK
    HNO; 1981 Mar; 29(3):95-7. PubMed ID: 7216849
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [123I-scintigraphy and perchlorate depletion test in the diagnosis of congenital hypothyroidism].
    Meller J; Zappel H; Conrad M; Roth C; Emrich D; Becker W
    Nuklearmedizin; 1998 Jan; 37(1):7-11. PubMed ID: 9467163
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [Euthyroid goiter with and without functional autonomy in the euthyroid phase: a comparison].
    Hillenhinrichs H; Emrich D
    Nuklearmedizin; 1998 May; 37(3):95-100. PubMed ID: 9604229
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan.
    Lai CC; Chiu CY; Shiao AS; Tso YC; Wu YC; Tu TY; Jap TS
    Metabolism; 2007 Sep; 56(9):1279-84. PubMed ID: 17697873
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Global 99mTc uptake in the differential diagnosis of a normal thyroid,goiter with euthyroidism and thyroid autonomy in an area of iodine deficiency].
    Kreisig T; Pickardt CR; Horn K; Bechtner G; Vaitl C; Kirsch CM; Knesewitsch P
    Nuklearmedizin; 1990 Jun; 29(3):113-9. PubMed ID: 2168038
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation.
    Masmoudi S; Charfedine I; Hmani M; Grati M; Ghorbel AM; Elgaied-Boulila A; Drira M; Hardelin JP; Ayadi H
    Am J Med Genet; 2000 Jan; 90(1):38-44. PubMed ID: 10602116
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Differential diagnosis between Pendred and pseudo-Pendred syndromes: clinical, radiologic, and molecular studies.
    Fugazzola L; Cerutti N; Mannavola D; Crino A; Cassio A; Gasparoni P; Vannucchi G; Beck-Peccoz P
    Pediatr Res; 2002 Apr; 51(4):479-84. PubMed ID: 11919333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Follicular carcinoma thyroid in Pendred syndrome.
    Bashir EA; Ahmed S; Murtaza B; Abbasi MH; Shah SS; Tamimy MS; Awan AS
    J Coll Physicians Surg Pak; 2004 Nov; 14(11):679-80. PubMed ID: 15530279
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Five cases of absence of iodide concentrating mechanism.
    Toyoshima K; Matsumoto Y; Nishida M; Yabuuchi H
    Acta Endocrinol (Copenh); 1977 Mar; 84(3):527-37. PubMed ID: 576528
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Hyperthyroidism in the thyroid hormone treatment of iodine deficiency goiter].
    Emrich D; Klaushenke G
    Dtsch Med Wochenschr; 1986 Apr; 111(15):577-81. PubMed ID: 3082613
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.