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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

193 related items for PubMed ID: 8293160

  • 1.
    ; . PubMed ID:
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  • 2. Transient cytoplasmic bodies in muscle of three infants with Werdnig-Hoffmann disease.
    Buchino JJ, Bove KE, Iannaccone ST.
    Pediatr Pathol; 1990; 10(4):563-73. PubMed ID: 2164661
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  • 3. [Infantile spinal muscular atrophy. Description of 2 cases of Werdnig-Hoffmann disease].
    Priora U, Quaglia P, Vivalda M, Giachino-Amistà MT, Domeneghetti G, Sardi R.
    Minerva Pediatr; 1987 Sep 30; 39(17-18):709-14. PubMed ID: 3437861
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  • 5. Spinal muscular atrophy.
    Wessel HB.
    Pediatr Ann; 1989 Jul 30; 18(7):421-7. PubMed ID: 2666923
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  • 6. [Spinal muscular atrophy].
    Porro G, Carboni P.
    Riv Neurol; 1988 Jul 30; 58(2):45-9. PubMed ID: 3051286
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  • 8. Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.
    Boylan KB, Cornblath DR.
    Ann Neurol; 1992 Sep 30; 32(3):404-7. PubMed ID: 1416812
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  • 9. Spinal muscular atrophy with respiratory distress type 1 (SMARD1).
    Kaindl AM, Guenther UP, Rudnik-Schöneborn S, Varon R, Zerres K, Schuelke M, Hübner C, von Au K.
    J Child Neurol; 2008 Feb 30; 23(2):199-204. PubMed ID: 18263757
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  • 11. [Nusinersen in the treatment of 4 children with presymptomatic spinal muscular atrophy].
    Feng YJ, Yu YC, Yan Y, Xu L, Zhao CY, Sheng GX, Chen C, Yang RL, Chen TT, Gao F, Mao SS.
    Zhonghua Er Ke Za Zhi; 2024 Aug 02; 62(8):786-788. PubMed ID: 39039883
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  • 14. [The spectrum of spinal muscular atrophies: a population study].
    Rudenskaia GE, Mamedova RA.
    Zh Nevrol Psikhiatr Im S S Korsakova; 1997 Aug 02; 97(8):22-5. PubMed ID: 9343477
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  • 15. Adult-onset motor neuron disease and infantile Werdnig-Hoffmann disease (spinal muscular atrophy type 1) in the same family.
    Shaw PJ, Ince PG, Goodship J, Burn J, Slade J, Bates D, Medwin DG.
    Neurology; 1992 Aug 02; 42(8):1477-80. PubMed ID: 1641139
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  • 16. [Spinal muscular atrophy in young infants].
    Smit LM, Hageman EG.
    Tijdschr Kindergeneeskd; 1989 Jun 02; 57(3):102-6. PubMed ID: 2799798
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  • 19. Congenital cytoplasmic body myopathy with survival motor neuron gene deletion or Werdnig-Hoffmann disease.
    Vajsar J, Balslev T, Ray PN, Siegel-Bartelt J, Jay V.
    Neurology; 1998 Sep 02; 51(3):873-5. PubMed ID: 9748045
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