BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 2582634)

  • 1. The variable intrafamiliar expressivity in Pendred's syndrome.
    Johnsen T; Sørensen MS; Feldt-Rasmussen U; Friis J
    Clin Otolaryngol Allied Sci; 1989 Oct; 14(5):395-9. PubMed ID: 2582634
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pendred's syndrome: a study of patients and relatives.
    Jamal MN; Arnaout MA; Jarrar R
    Ann Otol Rhinol Laryngol; 1995 Dec; 104(12):957-62. PubMed ID: 7492068
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome.
    Gausden E; Armour JA; Coyle B; Coffey R; Hochberg Z; Pembrey M; Britton KE; Grossman A; Reardon W; Trembath R
    Clin Endocrinol (Oxf); 1996 Apr; 44(4):441-6. PubMed ID: 8706311
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    J Clin Endocrinol Metab; 2000 Jul; 85(7):2469-75. PubMed ID: 10902795
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    J Clin Endocrinol Metab; 1999 Jan; 84(1):336-41. PubMed ID: 9920104
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Aggressive metastatic follicular thyroid carcinoma with anaplastic transformation arising from a long-standing goiter in a patient with Pendred's syndrome.
    Camargo R; Limbert E; Gillam M; Henriques MM; Fernandes C; Catarino AL; Soares J; Alves VA; Kopp P; Medeiros-Neto G
    Thyroid; 2001 Oct; 11(10):981-8. PubMed ID: 11716048
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fifteen cases of Pendred's syndrome. Congenital deafness and sporadic goiter.
    Illum P; Kiaer HW; Hvidberg-Hansen J; Sondergaard G
    Arch Otolaryngol; 1972 Oct; 96(4):297-304. PubMed ID: 4343141
    [No Abstract]   [Full Text] [Related]  

  • 8. Pendred's syndrome. Acoustic, vestibular and radiological findings in 17 unrelated patients.
    Johnsen T; Larsen C; Friis J; Hougaard-Jensen F
    J Laryngol Otol; 1987 Nov; 101(11):1187-92. PubMed ID: 3694034
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mondini cochlea in Pendred's syndrome. A histological study.
    Johnsen T; Jørgensen MB; Johnsen S
    Acta Otolaryngol; 1986; 102(3-4):239-47. PubMed ID: 3776519
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Pendred's syndrome: a clinical and biochemical study of abnormal thyroid hormone synthesis associated with congenital deaf-mutism].
    de Medeiros-Netto GA; Nicolau W; Cintra AB
    Rev Paul Med; 1969 Feb; 74(2):53-74. PubMed ID: 4190511
    [No Abstract]   [Full Text] [Related]  

  • 12. CT-scanning of the cochlea in Pendred's syndrome.
    Johnsen T; Videbaek H; Olesen KP
    Clin Otolaryngol Allied Sci; 1989 Oct; 14(5):389-93. PubMed ID: 2582633
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [Genetic characterization of Pendred's syndrome and study of thyroid function by double isotope labeling].
    Medeiros-Neto GA; Toledo SP
    Rev Hosp Clin Fac Med Sao Paulo; 1972; 27(3):115-22. PubMed ID: 4114174
    [No Abstract]   [Full Text] [Related]  

  • 15. Two Chinese families with Pendred's syndrome--radiological imaging of the ear and molecular analysis of the pendrin gene.
    Yong AM; Goh SS; Zhao Y; Eng PH; Koh LK; Khoo DH
    J Clin Endocrinol Metab; 2001 Aug; 86(8):3907-11. PubMed ID: 11502831
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pendred's syndrome: identification of the genetic defect a century after its recognition.
    Kopp P
    Thyroid; 1999 Jan; 9(1):65-9. PubMed ID: 10037079
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Pendred's syndrome: a cause of goiter associated with deafness].
    Vázquez AG; Montesinos IG; Jiménez AM; García JA; García JG; Hernández JA
    Endocrinol Nutr; 2009 Oct; 56(8):428-30. PubMed ID: 19959154
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Pendred's syndrome. Current features].
    Wémeau JL; Vlaeminck-Guillem V; Dubrulle F; Dumur V; Vincent C
    Presse Med; 2001 Nov; 30(34):1689-94. PubMed ID: 11760600
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Sporadic goiter and congenital deafness. Pendred's syndrome. 15 cases].
    Kiaer HW; Hvidberg-Hansen J
    Ugeskr Laeger; 1970 Sep; 132(39):1824-30. PubMed ID: 4319409
    [No Abstract]   [Full Text] [Related]  

  • 20. A novel mutation in the pendrin gene associated with Pendred's syndrome.
    Bogazzi F; Raggi F; Ultimieri F; Campomori A; Cosci C; Berrettini S; Neri E; La Rocca R; Ronca G; Martino E; Bartalena L
    Clin Endocrinol (Oxf); 2000 Mar; 52(3):279-85. PubMed ID: 10718825
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.