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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

134 related items for PubMed ID: 2918537

  • 1. Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?
    Boltshauser E, Lang W, Spillmann T, Hof E.
    J Med Genet; 1989 Feb; 26(2):105-8. PubMed ID: 2918537
    [Abstract] [Full Text] [Related]

  • 2. Distal spinal muscular atrophy with vocal cord paralysis.
    Pridmore C, Baraitser M, Brett EM, Harding AE.
    J Med Genet; 1992 Mar; 29(3):197-9. PubMed ID: 1552559
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Facioscapulohumeral muscular dystrophy and accompanying hearing loss.
    Meyerson MD, Lewis E, Ill K.
    Arch Otolaryngol; 1984 Apr; 110(4):261-6. PubMed ID: 6704043
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness.
    McEntagart M, Dunstan M, Bell C, Boltshauser E, Donaghy M, Harper PS, Williams N, Teare MD, Rahman N.
    J Neurol Neurosurg Psychiatry; 2002 Dec; 73(6):762-5. PubMed ID: 12438487
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Distal spinal muscular atrophy with vocal cord paralysis (dSMA-VII) is not linked to the MPD2 locus on chromosome 5q31.
    McEntagart M, Spurlock G, Jackson C, Harper P, Rahman N.
    J Med Genet; 2000 Aug; 37(8):E14. PubMed ID: 10922394
    [No Abstract] [Full Text] [Related]

  • 9. [Congenital facioscapulohumeral muscular dystrophy associated with tongue atrophy and sensorineural hearing disturbance].
    Shimizu T, Miyamoto K, Hayashi H, Nagashima T, Hirose K, Tanabe H.
    Rinsho Shinkeigaku; 1991 Apr; 31(4):433-8. PubMed ID: 1914330
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Familial auditory neuropathy.
    Wang Q, Gu R, Han D, Yang W.
    Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945
    [Abstract] [Full Text] [Related]

  • 12. Intrafamilial variable hearing loss in TRPV4 induced spinal muscular atrophy.
    Oonk AM, Ekker MS, Huygen PL, Kunst HP, Kremer H, Schelhaas JJ, Pennings RJ.
    Ann Otol Rhinol Laryngol; 2014 Dec; 123(12):859-65. PubMed ID: 24963089
    [Abstract] [Full Text] [Related]

  • 13. Hereditary neuropathy and vocal cord paralysis in a man with childhood diphtheria.
    Reichler BD, Scelsa SN, Simpson DM.
    Muscle Nerve; 2000 Jan; 23(1):132-7. PubMed ID: 10590420
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Vocal cord paresis and diaphragmatic dysfunction are severe and frequent symptoms of GDAP1-associated neuropathy.
    Sevilla T, Jaijo T, Nauffal D, Collado D, Chumillas MJ, Vilchez JJ, Muelas N, Bataller L, Domenech R, Espinós C, Palau F.
    Brain; 2008 Nov; 131(Pt 11):3051-61. PubMed ID: 18812441
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Familial systemic amyloidosis associated with bilateral sensorineural hearing loss and bilateral facial palsies.
    Hornigold R, Patel AV, Ward VM, O'Connor AF.
    J Laryngol Otol; 2006 Sep; 120(9):778-80. PubMed ID: 16870032
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.