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PUBMED FOR HANDHELDS

Journal Abstract Search


127 related items for PubMed ID: 7149664

  • 21. [Atypical facioscapulohumeral muscular dystrophy associated with congenital facial diplegia noted during infancy].
    Miyazaki M, Tawara S, Terao A, Araki S, Shirabe T.
    Rinsho Shinkeigaku; 1976 Jan; 16(1):32-8. PubMed ID: 943262
    [No Abstract] [Full Text] [Related]

  • 22. Vascular tortuosity and Coats'-like retinal changes in facioscapulohumeral muscular dystrophy.
    Tekin NF, Saatci AO, Kavukçu S.
    Ophthalmic Surg Lasers; 2000 Jan; 31(1):82-3. PubMed ID: 10976570
    [No Abstract] [Full Text] [Related]

  • 23. Hearing loss associated with progressive ataxia (Lichtenstein-Knorr disease?). Report of a sporadic case with peculiar neuroradiological findings.
    Striano S, Barbieri F, Meo R, Bilo L, Cirillo S.
    Acta Neurol (Napoli); 1989 Oct; 11(5):351-9. PubMed ID: 2603781
    [Abstract] [Full Text] [Related]

  • 24. Restricted myositis with myoedema simulating facioscapulohumeral muscular dystrophy.
    Rothstein TL, Carlson CB.
    Neurology; 1970 Apr; 20(4):386-7. PubMed ID: 5535006
    [No Abstract] [Full Text] [Related]

  • 25. [A case report of Cogan's syndrome (author's transl)].
    Niimi M, Kurata N, Ofuji T, Shiraga F, Ueno H, Hasegawa E, Matsuo N, Saito R.
    Nihon Naika Gakkai Zasshi; 1982 Apr 10; 71(4):513-8. PubMed ID: 7108333
    [No Abstract] [Full Text] [Related]

  • 26. Musical hallucinations in a deaf elderly patient.
    Miller TC, Crosby TW.
    Ann Neurol; 1979 Mar 10; 5(3):301-2. PubMed ID: 443762
    [Abstract] [Full Text] [Related]

  • 27. [Facioscapulohumeral muscular dystrophy (FSH) and hearing loss].
    Takeya T, Hamano K, Kawashima K, Iwasaki N, Ohhashi T, Sato T.
    No To Hattatsu; 1990 Jan 10; 22(1):24-9. PubMed ID: 2294949
    [Abstract] [Full Text] [Related]

  • 28. Facioscapulohumeral muscular dystrophy and accompanying hearing loss.
    Meyerson MD, Lewis E, Ill K.
    Arch Otolaryngol; 1984 Apr 10; 110(4):261-6. PubMed ID: 6704043
    [Abstract] [Full Text] [Related]

  • 29. The patient's view: Usher's syndrome.
    Can J Ophthalmol; 1980 Jan 10; 15(1):51-3. PubMed ID: 7378891
    [No Abstract] [Full Text] [Related]

  • 30. Retinal telangiectasis in scapuloperoneal muscular dystrophy.
    Dickey JB, Daily MJ.
    Am J Ophthalmol; 1991 Sep 15; 112(3):348-9. PubMed ID: 1882951
    [No Abstract] [Full Text] [Related]

  • 31. Severe fascioscapulohumeral muscular dystrophy presenting with Coats' disease and mental retardation.
    Bindoff LA, Mjellem N, Sommerfelt K, Krossnes BK, Roberts F, Krohn J, Tranheim RS, Haggerty ID.
    Neuromuscul Disord; 2006 Oct 15; 16(9-10):559-63. PubMed ID: 16935506
    [Abstract] [Full Text] [Related]

  • 32. Retinal telangiectasis in facioscapulohumeral muscular dystrophy with deafness.
    Gurwin EB, Fitzsimons RB, Sehmi KS, Bird AC.
    Arch Ophthalmol; 1985 Nov 15; 103(11):1695-700. PubMed ID: 4062636
    [Abstract] [Full Text] [Related]

  • 33. Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy. A general association with genetic and therapeutic implications.
    Fitzsimons RB, Gurwin EB, Bird AC.
    Brain; 1987 Jun 15; 110 ( Pt 3)():631-48. PubMed ID: 3580827
    [Abstract] [Full Text] [Related]

  • 34. Facioscapulohumeral dystrophy, retinal vasculature, and Sneddon's syndrome.
    Coleman RJ, Ingram DA, Swash M.
    Muscle Nerve; 1990 Aug 15; 13(8):759. PubMed ID: 2385262
    [No Abstract] [Full Text] [Related]

  • 35. Differential diagnosis of scapuloperoneal syndrome.
    Milanov I, Ishpekova B.
    Electromyogr Clin Neurophysiol; 1997 Mar 15; 37(2):73-8. PubMed ID: 9098670
    [Abstract] [Full Text] [Related]

  • 36. Hearing impairment and paraphrenia.
    Eastwood R, Corbin S, Reed M.
    J Otolaryngol; 1981 Aug 15; 10(4):306-8. PubMed ID: 7299887
    [Abstract] [Full Text] [Related]

  • 37. [Facial-scapular-humeral myodystrophy (genetic and clinical features)].
    Bogorodinskiĭ DK, Znoĭko ZV, Kazakov VM, Skoromets AA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973 Aug 15; 73(6):801-9. PubMed ID: 4753589
    [No Abstract] [Full Text] [Related]

  • 38. The facio-scapulo-limb (or the facioscapulohumeral) type of muscular dystrophy. Clinical and genetic study of 200 cases.
    Kazakov VM, Bogorodinsky DK, Znoyko ZV, Skorometz AA.
    Eur Neurol; 1974 Aug 15; 11(4):236-60. PubMed ID: 4854830
    [No Abstract] [Full Text] [Related]

  • 39. [Effect of moderate hearing loss on speech development in children].
    Zaleski T.
    Otolaryngol Pol; 1984 Aug 15; 38(4):323-6. PubMed ID: 6522055
    [No Abstract] [Full Text] [Related]

  • 40. [Landouzy-Dejerine syndrome. Evolution of the concept of facio-scapulo-humeral amyotrophia].
    Schmitt J, Barrucand D, Schmidt C.
    Rev Neurol (Paris); 1977 Apr 15; 133(4):279-82. PubMed ID: 929032
    [Abstract] [Full Text] [Related]


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