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 *

78 related articles for article (PubMed ID: 6625373)

  • 21. 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]  

  • 22. Enlarged endolymphatic duct and sac syndrome: relationship between MR findings and genotype of mutation in Pendred syndrome gene.
    Naganawa S; Koshikawa T; Fukatsu H; Ishigaki T; Sato E; Sugiura M; Yoshino T; Nakashima T
    Magn Reson Imaging; 2004 Jan; 22(1):25-30. PubMed ID: 14972391
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pendred's syndrome and non-syndromic DFNB4 deafness associated with the homozygous T410M mutation in the SLC26A4 gene in siblings.
    Arellano B; Pera A; Ramírez-Camacho R; Villamar M; Trinidad A; García JR; Moreno F; Hernández-Chico C
    Clin Genet; 2005 May; 67(5):438-40. PubMed ID: 15811013
    [No Abstract]   [Full Text] [Related]  

  • 24. 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]  

  • 25. [Genetic deafness and Pendred syndrome].
    Ayerbe I; Négrevergne M; Sanchez Fernandez JM; Ucelay R; Albisu Y
    Rev Laryngol Otol Rhinol (Bord); 1997; 118(2):113-7. PubMed ID: 9297919
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Retinitis pigmentosa, vitiligo and deaf-mutism. Apropos of a case].
    Cernea P; Damien C
    J Fr Ophtalmol; 1994; 17(8-9):501-3. PubMed ID: 7989657
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Two families with Pendred's syndrome].
    Etzioni A; Benderly ; Levy J
    Harefuah; 1980 Dec; 99(12):425-6. PubMed ID: 6265330
    [No Abstract]   [Full Text] [Related]  

  • 28. Pendred's syndrome.
    Pearce JM
    Eur Neurol; 2007; 58(3):189-90. PubMed ID: 17622729
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Case of nephrotic syndrome with goiter].
    Ciepielewska D; Sieniawska M
    Pediatr Pol; 1965 Nov; 40(11):1263-5. PubMed ID: 5861754
    [No Abstract]   [Full Text] [Related]  

  • 30. [Sporadic familial goitrous deaf-mutism and endemic familial goitrous deaf-mutism].
    COSTA A; FERRARIS GM
    Ann Endocrinol (Paris); 1963; 24():23-38. PubMed ID: 14023257
    [No Abstract]   [Full Text] [Related]  

  • 31. [Deaf-mutism in the Piedmont areas of endemic goiter].
    COSTA A; FERRARIS GM; PATRITO G; BO V; LAVAZZA L
    Folia Endocrinol; 1963 Apr; 16():151-67. PubMed ID: 14023256
    [No Abstract]   [Full Text] [Related]  

  • 32. [An unusual coincidence: elective mutism and sleep-related bioelectric seizure status syndrome].
    Strehlow U; Kirchmann HM; Schäfer H
    Prax Kinderpsychol Kinderpsychiatr; 1993; 42(5):157-60. PubMed ID: 8337211
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The Pendred syndrome gene encodes a chloride-iodide transport protein.
    Scott DA; Wang R; Kreman TM; Sheffield VC; Karniski LP
    Nat Genet; 1999 Apr; 21(4):440-3. PubMed ID: 10192399
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Selective mutism and mitochondrial disease: a description of a new association].
    Amado-Puentes A; Busto-Cuinas M; Gomez-Lado C; Perez-Gay L; Eiris-Punal J; Castro-Gago M
    Rev Neurol; 2010 Oct; 51(7):444-5. PubMed ID: 20859925
    [No Abstract]   [Full Text] [Related]  

  • 35. [Postoperative mutism in children with the posterior fossa tumors].
    Orlov IuA; Zentani S
    Zh Vopr Neirokhir Im N N Burdenko; 2001; (1):6-9; discussion 10. PubMed ID: 11544744
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A mutation in PDS causes non-syndromic recessive deafness.
    Li XC; Everett LA; Lalwani AK; Desmukh D; Friedman TB; Green ED; Wilcox ER
    Nat Genet; 1998 Mar; 18(3):215-7. PubMed ID: 9500541
    [No Abstract]   [Full Text] [Related]  

  • 37. The coexistence of goiter and deaf-mutism.
    FRIEDLIER OP
    Surgery; 1951 Sep; 30(3):496-9. PubMed ID: 14866692
    [No Abstract]   [Full Text] [Related]  

  • 38. [DEAF-MUTISM IN ENDEMIC GOITER].
    VITALE W
    Ann Laringol Otol Rinol Faringol; 1963; 62():347-51. PubMed ID: 14083888
    [No Abstract]   [Full Text] [Related]  

  • 39. [Goiter, endemic cretinism, deaf-mutism and blood groups of the ABO system].
    DELLA BEFFA A; MORTARA A; SERRA A
    Folia Endocrinol Mens Incretologia Incretoterapia; 1960 Oct; 13():670-80. PubMed ID: 13721597
    [No Abstract]   [Full Text] [Related]  

  • 40. Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment.
    López-Bigas N; Melchionda S; de Cid R; Grifa A; Zelante L; Govea N; Arbonés ML; Gasparini P; Estivill X
    Hum Mutat; 2001 Dec; 18(6):548. PubMed ID: 11748854
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.