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

113 related items for PubMed ID: 7180297

  • 1. [Proximal spinal muscular atrophies].
    Magalov ShI.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(11):18-22. PubMed ID: 7180297
    [Abstract] [Full Text] [Related]

  • 2. [Electoneuromyography in the study of diseases of the neuromuscular system].
    Skvortsov IA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(12):1642-9. PubMed ID: 525113
    [Abstract] [Full Text] [Related]

  • 3. [Clinical picture, pathogenesis and geneology of hereditary progressive spinal muscular atrophies].
    Nesterov LN, Sushcheva GP, Viatkina SIa, Novikova NP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):321-30. PubMed ID: 6326437
    [Abstract] [Full Text] [Related]

  • 4. [Clinicoelectroneuromyographic characteristics of neuralgic amyotrophy].
    Viatkina SIa, Novikova NP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(11):1650-5. PubMed ID: 6275642
    [Abstract] [Full Text] [Related]

  • 5. [Clinical electrodiagnostic findings in peroneal muscular atrophy (author's transl)].
    Leven B.
    Fortschr Neurol Psychiatr Grenzgeb; 1976 Nov; 44(11):661-70. PubMed ID: 1049563
    [Abstract] [Full Text] [Related]

  • 6. The genetic heterogeneity of spinal muscular atrophy (SMA).
    Zellweger H.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):82-9. PubMed ID: 5173130
    [Abstract] [Full Text] [Related]

  • 7. [Family with progressive myelopathic muscular atrophy with proximal distribution and onset in adulthood].
    Mapelli G.
    Riv Patol Nerv Ment; 1983 Feb; 104(4):159-70. PubMed ID: 6681331
    [Abstract] [Full Text] [Related]

  • 8. [Variability of hereditary spinal amyotrophies].
    Popoy'ian MD, Dubinskaia EE, Kabanova AE.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1979 Feb; 79(3):276-82. PubMed ID: 442895
    [Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. Electromyographic findings in different forms of infantile and juvenile proximal spinal muscular atrophy.
    Hausmanowa-Petrusewicz I, Karwańska A.
    Muscle Nerve; 1986 Jan 25; 9(1):37-46. PubMed ID: 3951479
    [Abstract] [Full Text] [Related]

  • 11. Autosomal dominant late adult spinal muscular atrophy, type Finkel.
    Richieri-Costa A, Rogatko A, Levisky R, Finkel N, Frota-Pessoa O.
    Am J Med Genet; 1981 Jan 25; 9(2):119-28. PubMed ID: 7258225
    [Abstract] [Full Text] [Related]

  • 12. [Genetics of child spinal amyotrophy : existence of 2 autosomal recessive forms].
    Feingold J, Arthuis M, Celers J.
    Ann Genet; 1977 Mar 25; 20(1):19-23. PubMed ID: 302668
    [Abstract] [Full Text] [Related]

  • 13. 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 Mar 25; 2(4):203-9. PubMed ID: 5146579
    [No Abstract] [Full Text] [Related]

  • 14. Spinal motoneuron function in lower motor neuron disease: normal corticomotoneuronal and peripheral Ia EPSPs in patients with spinal muscular atrophy.
    Gonschorek AS, Feistner H, Awiszus F.
    Electromyogr Clin Neurophysiol; 1999 Mar 25; 39(1):27-32. PubMed ID: 10076758
    [Abstract] [Full Text] [Related]

  • 15. [Hereditary spinal distal muscular atrophy (report of 2 cases)].
    Badalian LO, Timonina OV, Aingorn ED, Avakian GN, Koroleva IA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1980 Mar 25; 80(11):1614-7. PubMed ID: 7456910
    [No Abstract] [Full Text] [Related]

  • 16. Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: clinical picture, influence of gender, and genetic implications.
    Rudnik-Schöneborn S, Röhrig D, Morgan G, Wirth B, Zerres K.
    Am J Med Genet; 1994 May 15; 51(1):70-6. PubMed ID: 8030672
    [Abstract] [Full Text] [Related]

  • 17. [Terminal polineuropathy (independent clinical syndrome or variant course of myasthenia)].
    Gekht BM, Nikitin SS, Sanadze AG, Samoĭlov MI.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1983 May 15; 83(11):1611-20. PubMed ID: 6326436
    [Abstract] [Full Text] [Related]

  • 18. [Kennedy syndrome--bulbo-spinal muscular atrophy].
    Szabó A, Mechler F.
    Ideggyogy Sz; 2002 Sep 20; 55(9-10):323-9. PubMed ID: 12503246
    [Abstract] [Full Text] [Related]

  • 19. [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 Sep 20; 16(2):125-8. PubMed ID: 8078785
    [Abstract] [Full Text] [Related]

  • 20. The Kugelberg-Welander syndrome (hereditary proximal spinal muscular atrophy).
    Beighton PH.
    Birth Defects Orig Artic Ser; 1971 Feb 20; 7(2):99. PubMed ID: 5173132
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.