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Journal Abstract Search

145 related items for PubMed ID: 2614228

  • 41. [A new form of congenital hereditary deafness (Waardenburg's syndrome)].
    KEIZER DP.
    Ned Tijdschr Geneeskd; 1952 Oct 11; 96(41):2541-3. PubMed ID: 13025541
    [No Abstract] [Full Text] [Related]

  • 42. Upper limb involvement in the Klein-Waardenburg syndrome.
    Goodman RM, Lewithal I, Solomon A, Klein D.
    Am J Med Genet; 1982 Apr 11; 11(4):425-33. PubMed ID: 7091186
    [Abstract] [Full Text] [Related]

  • 43. The association of familial hyperbetalipoproteinaemia with Waardenburg's syndrome.
    Amer M, el-Shazly M.
    Br J Dermatol; 1974 Mar 11; 90(3):255-62. PubMed ID: 4823082
    [No Abstract] [Full Text] [Related]

  • 44. Otopathology in a case of type I Waardenburg's syndrome.
    Merchant SN, McKenna MJ, Baldwin CT, Milunsky A, Nadol JB.
    Ann Otol Rhinol Laryngol; 2001 Sep 11; 110(9):875-82. PubMed ID: 11558766
    [Abstract] [Full Text] [Related]

  • 45. Waardenburg's syndrome.
    Fanaroff AA, Levin SE.
    J Pediatr; 1968 Jul 11; 73(1):151. PubMed ID: 5658623
    [No Abstract] [Full Text] [Related]

  • 46. Progressive familial hearing loss in Muckle-Wells syndrome.
    Koitschev A, Gramlich K, Hansmann S, Benseler S, Plontke SK, Koitschev C, Koetter I, Kuemmerle-Deschner JB.
    Acta Otolaryngol; 2012 Jul 11; 132(7):756-62. PubMed ID: 22497426
    [Abstract] [Full Text] [Related]

  • 47. Clinical, dermatoglyphic and chromosomal study of Waardenburg's syndrome.
    Shiono H, Bandou K, Kadowaki J.
    Tohoku J Exp Med; 1969 Sep 11; 99(1):45-50. PubMed ID: 5349887
    [No Abstract] [Full Text] [Related]

  • 48. Familial sensorineural hearing loss: a correlative study of audiologic, radiographic, and vestibular findings.
    Chan KH, Eelkema EA, Furman JM, Kamerer DB.
    Ann Otol Rhinol Laryngol; 1991 Aug 11; 100(8):620-5. PubMed ID: 1872511
    [Abstract] [Full Text] [Related]

  • 49. Waardenburg syndrome type I with heterochromia iridis and circumscribed hypopigmentation of the skin.
    Eigelshoven S, Kameda G, Kortüm AK, Hübsch S, Angerstein W, Singh P, Vöhringer R, Goecke T, Mayatepek E, Ruzicka T, Wildhardt G, Meissner T, Kruse R.
    Pediatr Dermatol; 2009 Aug 11; 26(6):759-61. PubMed ID: 20199465
    [Abstract] [Full Text] [Related]

  • 50. Ophthalmological findings in 34 patients with Waardenburg syndrome.
    Delleman JW, Hageman MJ.
    J Pediatr Ophthalmol Strabismus; 1978 Aug 11; 15(6):341-5. PubMed ID: 105123
    [Abstract] [Full Text] [Related]

  • 51. Defect of neutrophil mobility with dominant inheritance in a family with Waardenberg's syndrome.
    Hayward AR, Mowla R, Harvey B.
    Arch Dis Child; 1981 Apr 11; 56(4):279-82. PubMed ID: 7247439
    [Abstract] [Full Text] [Related]

  • 52. The incidence and significance of the Tullio phenomenon in man.
    Erlich MA, Lawson W.
    Otolaryngol Head Neck Surg (1979); 1980 Apr 11; 88(5):630-5. PubMed ID: 6969384
    [Abstract] [Full Text] [Related]

  • 53. Congenital stapes malformation: Rare conductive hearing loss in a patient with Waardenburg syndrome.
    Melzer JM, Eliason M, Conley GS.
    Laryngoscope; 2016 Apr 11; 126(4):992-5. PubMed ID: 26152551
    [Abstract] [Full Text] [Related]

  • 54. Audio-vestibular disturbances in Behcet's patients: report of 62 cases.
    Kulahli I, Balci K, Koseoglu E, Yuce I, Cagli S, Senturk M.
    Hear Res; 2005 May 11; 203(1-2):28-31. PubMed ID: 15855027
    [Abstract] [Full Text] [Related]

  • 55. Inner ear dysfunction in myotonic dystrophy type 1.
    Balatsouras DG, Felekis D, Panas M, Xenellis J, Koutsis G, Kladi A, Korres SG.
    Acta Neurol Scand; 2013 May 11; 127(5):337-43. PubMed ID: 23121018
    [Abstract] [Full Text] [Related]

  • 56. Clinical features of the Waardenburg syndromes.
    Newton VE.
    Adv Otorhinolaryngol; 2002 May 11; 61():201-8. PubMed ID: 12408085
    [No Abstract] [Full Text] [Related]

  • 57. Possible central vestibular findings in a patient with a peripheral vestibular disorder.
    Brookler KH.
    Ear Nose Throat J; 2004 Aug 11; 83(8):520, 522. PubMed ID: 15487628
    [No Abstract] [Full Text] [Related]

  • 58. Cochlear implantation in patients with inner ear bone malformations with posterior labyrinth involvement: an exploratory study.
    Palomeque Vera JM, Platero Sánchez-Escribano M, Gómez Hervás J, Fernández Prada M, González Ramírez AR, Sainz Quevedo M.
    Eur Arch Otorhinolaryngol; 2016 Apr 11; 273(4):893-8. PubMed ID: 25971996
    [Abstract] [Full Text] [Related]

  • 59. [Heterochromia iridis, congenital deafness and skin pigmentary abnormalities: Waardenburg syndrome].
    Jiménez Gómez N, Ballester Martínez MA, Urrutia Hernando S, Jaén Olasolo P.
    Med Clin (Barc); 2014 Mar 20; 142(6):e11. PubMed ID: 24029453
    [No Abstract] [Full Text] [Related]

  • 60. [Hearing disorders in Waardenburg's syndrome].
    Schulze W, Ganz H.
    HNO; 1972 Jul 20; 20(7):203-7. PubMed ID: 5071320
    [No Abstract] [Full Text] [Related]

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