BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 5711032)

  • 1. Neurogenic muscular atrophy of infancy with prolonged survival--the variable course of Werdnig-Hoffmann disease.
    Munsat TL; Woods R
    Trans Am Neurol Assoc; 1968; 93():248-50. PubMed ID: 5711032
    [No Abstract]   [Full Text] [Related]  

  • 2. Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werdnig-Hoffmann Disease.
    Munsat TL; Woods R; Fowler W; Pearson CM
    Brain; 1969 Mar; 92(1):9-24. PubMed ID: 5774034
    [No Abstract]   [Full Text] [Related]  

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

  • 4. Spinal muscular atrophy.
    McLeod JG; Williams IM
    Minn Med; 1971 Jun; 54(6):457-61. PubMed ID: 5559368
    [No Abstract]   [Full Text] [Related]  

  • 5. [Electromyographic tracings of neurogenic type with muscular biopsies of myopathic type].
    Turner M; Dominelli JC
    Prensa Med Argent; 1970 Dec; 57(41):1913-7. PubMed ID: 5509206
    [No Abstract]   [Full Text] [Related]  

  • 6. [Electromyogram and Werdnig-Hoffmann disease].
    GAUDIER B; MILBLED G; RAMEZ T
    J Radiol Electrol Med Nucl; 1962; 43():426-8. PubMed ID: 13897277
    [No Abstract]   [Full Text] [Related]  

  • 7. [Value of the muscular responses evoked by electric impulses in the diagnosis of heredodegenerative muscular atrophy].
    Călcăianu G; Tudor I
    Neurol Psihiatr Neurochir; 1967; 12(6):539-44. PubMed ID: 5593230
    [No Abstract]   [Full Text] [Related]  

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

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

  • 10. [Familial neurogenic amyotrophy, similar to Charcot-Marie-Tooth disease. Clinical and ultrastructural study].
    Vital C; Julien J; Vallat JM; Le Blanc M
    Rev Neurol (Paris); 1970 Jan; 122(1):15-28. PubMed ID: 5433253
    [No Abstract]   [Full Text] [Related]  

  • 11. [Clinical course of Werdnig-Hoffmann spinal amyotrophy].
    Drobinskiĭ AD; Klimenko AV
    Klin Med (Mosk); 1976 Sep; 54(9):87-90. PubMed ID: 1003924
    [No Abstract]   [Full Text] [Related]  

  • 12. The diagnosis of some neuromuscular disorders of infancy and childhood.
    Bharucha EP; Iyer CG; Bharucha PE; Mulla-Firoz PK
    Neurol India; 1966; 14(4):178-83. PubMed ID: 5977715
    [No Abstract]   [Full Text] [Related]  

  • 13. Late progressive muscular atrophy and antecedent poliomyelitis.
    Alter M; Kurland LT; Molgaard CA
    Adv Neurol; 1982; 36():303-9. PubMed ID: 6983825
    [No Abstract]   [Full Text] [Related]  

  • 14. [Electromyography in Charcot-Marie disease].
    Zumstein V; Schneider C
    Schweiz Arch Neurol Neurochir Psychiatr; 1982; 130(2):297-307. PubMed ID: 7134908
    [No Abstract]   [Full Text] [Related]  

  • 15. [Infantile neurogenic amyotrophies with prolonged course: the problem of their nosologic classification in relation to Werdnig-Hoffmann's disease].
    Lugaresi E; Giovanardi-Rossi P; Gambetti P
    Riv Sper Freniatr Med Leg Alien Ment; 1965 Jun; 89(3):594-619. PubMed ID: 5845541
    [No Abstract]   [Full Text] [Related]  

  • 16. Is Kugelberg-Welander spinal muscular atrophy a fetal defect?
    Hausmanowa-Petrusewicz I; Fidziańska A; Niebrój-Dobosz I; Strugalska MH
    Muscle Nerve; 1980; 3(5):389-402. PubMed ID: 7421874
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Variants of neuromuscular pathology in a case of familial-hereditary disease (the Werdnig-Hoffman syndrome and the Wolfart-Kugelberg-Welander syndrome in two sisters)].
    Il'ina NA; Sosnovskaia LS; Kogan EI; Kalmykova LG
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1969; 69(6):817-22. PubMed ID: 5370144
    [No Abstract]   [Full Text] [Related]  

  • 18. [A case of Werdnig-Hoffmann disease in a 6-month-old child].
    Wazna S; Warakomska-Grzycka S
    Przegl Lek; 1966; 22(6):457-9. PubMed ID: 5912249
    [No Abstract]   [Full Text] [Related]  

  • 19. [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]  

  • 20. [Neurophysiologic aspects of progressive spinal amyotrophies].
    Krstić S; Radojicić B
    Neurologija; 1979; 27(1-4):121-6. PubMed ID: 261999
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.