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Journal Abstract Search

303 related items for PubMed ID: 6855803

  • 1. Spinal muscular atrophy: the natural course of disease.
    Russman BS, Melchreit R, Drennan JC.
    Muscle Nerve; 1983; 6(3):179-81. PubMed ID: 6855803
    [Abstract] [Full Text] [Related]

  • 2. Electromyographic findings in different forms of infantile and juvenile proximal spinal muscular atrophy.
    Hausmanowa-Petrusewicz I, Karwańska A.
    Muscle Nerve; 1986 Jan; 9(1):37-46. PubMed ID: 3951479
    [Abstract] [Full Text] [Related]

  • 3. [Intermediate forms of infantile spinal amyotrophy. Apropos of 20 personal observations].
    Pou-Serradell A, Montserrat L, Ugarte A.
    Rev Neurol (Paris); 1978 Jan; 134(1):35-44. PubMed ID: 674984
    [Abstract] [Full Text] [Related]

  • 4. Some electrophysiological and immunological problems in Werdnig--Hoffmann disease.
    Ryniewicz B.
    Acta Univ Carol Med Monogr; 1976 Jan; (75):37-8. PubMed ID: 1052639
    [No Abstract] [Full Text] [Related]

  • 5. [Progressive infantile spinal atrophy. Werdnig-Hoffmann disease].
    Sotelo-Cruz N, Torres-Cárdenas O, Gallegos-Gardner M.
    Bol Med Hosp Infant Mex; 1984 Jul; 41(7):387-92. PubMed ID: 6477703
    [No Abstract] [Full Text] [Related]

  • 6. Sensory nerve conduction in the spinal muscular atrophies.
    Schwartz MS, Moosa A.
    Dev Med Child Neurol; 1977 Feb; 19(1):50-3. PubMed ID: 844665
    [Abstract] [Full Text] [Related]

  • 7. Spinal muscular atrophy: experience in diagnosis and rehabilitation management of 60 patients.
    Eng GD, Binder H, Koch B.
    Arch Phys Med Rehabil; 1984 Sep; 65(9):549-53. PubMed ID: 6477090
    [Abstract] [Full Text] [Related]

  • 8. Spinal muscular atrophy: survival pattern and functional status.
    Chung BH, Wong VC, Ip P.
    Pediatrics; 2004 Nov; 114(5):e548-53. PubMed ID: 15492357
    [Abstract] [Full Text] [Related]

  • 9. [Familial occurrence of Kugelberg-Welander pseudomyopathic spinal muscular atrophy].
    Zeiler K, Mamoli B, Heiss WD.
    Nervenarzt; 1976 Jul; 47(7):444-8. PubMed ID: 958547
    [No Abstract] [Full Text] [Related]

  • 10. [Werding-Hoffmann disease and Kugelberg-Welander disease].
    Uono M.
    No To Shinkei; 1970 Aug; 22(8):902-6. PubMed ID: 5468436
    [No Abstract] [Full Text] [Related]

  • 11. Electromyographic analysis in spinal progressive muscular atrophy, juvenile unilateral muscular atrophy, neural progressive muscular atrophy and myeloradiculoneuritis.
    Iida M, Fujiwara R, Yamamura Y.
    Nagoya J Med Sci; 1966 Dec; 29(2):105-17. PubMed ID: 5984523
    [No Abstract] [Full Text] [Related]

  • 12. [Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy].
    Spiegel R, Hagmann A, Boltshauser E, Moser H.
    Schweiz Med Wochenschr; 1996 May 25; 126(21):907-14. PubMed ID: 8693311
    [Abstract] [Full Text] [Related]

  • 13. Scapuloperoneal muscular atrophy: Davidenkow's syndrome. Family report.
    Milanov I, Georgiev D, Krushkov C.
    Electromyogr Clin Neurophysiol; 1996 May 25; 36(5):259-63. PubMed ID: 8877316
    [Abstract] [Full Text] [Related]

  • 14. [Bioelectric characteristics of spinal muscular atrophy].
    Hausmanowa-Petrusewicz I.
    Neurol Neurochir Pol; 1983 May 25; 17(2):171-6. PubMed ID: 6633794
    [Abstract] [Full Text] [Related]

  • 15. Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease).
    Fried K, Emery AE.
    Clin Genet; 1971 May 25; 2(4):203-9. PubMed ID: 5146579
    [No Abstract] [Full Text] [Related]

  • 16. [Infantile spinal muscular atrophy].
    Barois A, Estournet B, Duval-Beaupère G, Bataille J, Leclair-Richard D.
    Rev Neurol (Paris); 1989 May 25; 145(4):299-304. PubMed ID: 2660222
    [Abstract] [Full Text] [Related]

  • 17. Motor and sensory conduction velocity in spinal muscular atrophy. Follow-up study.
    Ryniewicz B.
    Electromyogr Clin Neurophysiol; 1977 May 25; 17(5):385-91. PubMed ID: 604062
    [No Abstract] [Full Text] [Related]

  • 18. [Heart involvement in progressive spinal muscular atrophy. A review of the literature and case histories in childhood].
    Distefano G, Sciacca P, Parisi MG, Parano E, Smilari P, Marletta M, Fiumara A.
    Pediatr Med Chir; 1994 May 25; 16(2):125-8. PubMed ID: 8078785
    [Abstract] [Full Text] [Related]

  • 19. [A case of Wohlfart-Kugelberg-Welander disease or hereditary familial spinal juvenile muscular atrophy].
    Manara F, Gasco P, Milani L.
    Minerva Med; 1977 Feb 04; 68(6):417-24. PubMed ID: 840437
    [No Abstract] [Full Text] [Related]

  • 20. [Neonatal muscular spinal atrophy: a case report].
    Pavone P, Velardita M, Trigilia T, Luca G, Lucenti C, Romeo G, Falsaperla R.
    Pediatr Med Chir; 2004 Feb 04; 26(2):139-41. PubMed ID: 15700740
    [Abstract] [Full Text] [Related]

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