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 *

67 related articles for article (PubMed ID: 943262)

  • 1. [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]  

  • 2. Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness.
    Korf BR; Bresnan MJ; Shapiro F; Sotrel A; Abroms IF
    Ann Neurol; 1985 May; 17(5):513-6. PubMed ID: 4004175
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Chronic spinal muscular atrophy of facioscapulohumeral type with congenital facial palsy in twins (author's transl)].
    Iwamoto N; Koh CS; Oguchi K; Yanagisawa N; Tsukagoshi H
    Rinsho Shinkeigaku; 1979 May; 19(5):301-7. PubMed ID: 477132
    [No Abstract]   [Full Text] [Related]  

  • 5. [Congenital bilateral paralysis of the facial nerve].
    Vajda P; Szabová I
    Cesk Pediatr; 1974 Sep; 29(9):486-8. PubMed ID: 4420551
    [No Abstract]   [Full Text] [Related]  

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

  • 7. Inflammatory facioscapulohumeral muscular dystrophy and Coats syndrome.
    Wulff JD; Lin JT; Kepes JJ
    Ann Neurol; 1982 Oct; 12(4):398-401. PubMed ID: 7149665
    [No Abstract]   [Full Text] [Related]  

  • 8. Facioscapulohumeral dystrophy associated with hearing loss and Coats syndrome.
    Taylor DA; Carroll JE; Smith ME; Johnson MO; Johnston GP; Brooke MH
    Ann Neurol; 1982 Oct; 12(4):395-8. PubMed ID: 7149664
    [No Abstract]   [Full Text] [Related]  

  • 9. Facioscapulohumeral muscular dystrophy with congenital absence of sternocleidomastoid muscles.
    Penchaszadeh V
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):116-7. PubMed ID: 5173120
    [No Abstract]   [Full Text] [Related]  

  • 10. [A case of facioscapulohumeral muscular dystrophy complicated with complete A-V block].
    Ohno Y; Nakata Y; Sumiyoshi M; Hisaoka T; Ogura S; Nakazato Y; Yamaguchi H
    Kokyu To Junkan; 1991 May; 39(5):491-5. PubMed ID: 2068409
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Infantile facioscapulohumeral muscular dystrophy].
    Badalian LO; Temin PA; Mukhin KIu; Bulaeva NV; Zavadenko NN; Nikanorova MIu; Shnaĭdman RV; Lysov VL
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1992; 92(3):28-30. PubMed ID: 1332322
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Möbius syndrome and facioscapulohumeral muscular dystrophy.
    Hanson PA; Rowland LP
    Arch Neurol; 1971 Jan; 24(1):31-9. PubMed ID: 5538600
    [No Abstract]   [Full Text] [Related]  

  • 13. De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1).
    Jardine PE; Koch MC; Lunt PW; Maynard J; Bathke KD; Harper PS; Upadhyaya M
    Arch Dis Child; 1994 Sep; 71(3):221-7. PubMed ID: 7979495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Electromyographic study on congenital facial diplegia.
    Sumitsuji N; Tanaka M; Yuasa R
    Electromyography; 1970; 10(4):399-414. PubMed ID: 5521840
    [No Abstract]   [Full Text] [Related]  

  • 15. Locomotor problems in infantile facioscapulohumeral muscular dystrophy. Retrospective study of 9 patients.
    Shapiro F; Specht L; Korf BR
    Acta Orthop Scand; 1991 Aug; 62(4):367-71. PubMed ID: 1882679
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Atypical facet of Möbius syndrome: association with facioscapulohumeral muscular dystrophy.
    Kolski HK; Leonard NJ; Lemmers RJ; Bamforth JS
    Muscle Nerve; 2008 Apr; 37(4):526-9. PubMed ID: 18059038
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Permanent paralysis of the atrium in a patient with facioscapulohumeral muscular dystrophy.
    Baldwin BJ; Talley RC; Johnson C; Nutter DO
    Am J Cardiol; 1973 May; 31(5):649-53. PubMed ID: 4698137
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. The Moebius syndrome: bilateral facial diplegia. A discourse on the symptoms, pathology, and a surgical dynamic animation of the paralyzed face.
    Rubin LR
    Clin Plast Surg; 1976 Oct; 3(4):625-36. PubMed ID: 975734
    [No Abstract]   [Full Text] [Related]  

  • 20. [Spinal facioscapulo-peroneal (or facioscapulo-crural) muscular atrophy and facioscapulo-peroneal muscular dystrophy].
    Kazakov VM; Skoromets AA; Mikhaĭlov EP; Barantsevich ER
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(5):662-7. PubMed ID: 3739474
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.