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Journal Abstract Search

611 related items for PubMed ID: 25300987

  • 1. Congenital segmental spinal muscular atrophy: a case report.
    Savaş T, Erol I, Özkale Y, Saygi S.
    J Child Neurol; 2015 Mar; 30(4):509-12. PubMed ID: 25300987
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  • 2. [Very severe spinal muscular atrophy--type 0. A cause of congenital multiple arthrogryposis].
    Balslev T, Hertz JM, Rackauskaite G, Sørensen LA.
    Ugeskr Laeger; 2001 Oct 08; 163(41):5679-80. PubMed ID: 11665473
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  • 3. Congenital cervical spinal muscular atrophy: a non-familial, non progressive condition of the upper limbs.
    Hageman G, Ramaekers VT, Hilhorst BG, Rozeboom AR.
    J Neurol Neurosurg Psychiatry; 1993 Apr 08; 56(4):365-8. PubMed ID: 8482956
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  • 5. 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 08; 23(2):199-204. PubMed ID: 18263757
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  • 7. Congenital caudal spinal atrophy: a case report.
    Tsukamoto H, Inagaki M, Tomita Y, Ohno K.
    Neuropediatrics; 1992 Oct 08; 23(5):260-2. PubMed ID: 1454146
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  • 8. Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cells.
    Oates EC, Reddel S, Rodriguez ML, Gandolfo LC, Bahlo M, Hawke SH, Lamandé SR, Clarke NF, North KN.
    Brain; 2012 Jun 08; 135(Pt 6):1714-23. PubMed ID: 22628388
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  • 10. Severe lethal spinal muscular atrophy variant with arthrogryposis.
    Kizilates SU, Talim B, Sel K, Köse G, Caglar M.
    Pediatr Neurol; 2005 Mar 08; 32(3):201-4. PubMed ID: 15730903
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  • 12. Type 0 Spinal Muscular Atrophy: Further Delineation of Prenatal and Postnatal Features in 16 Patients.
    Grotto S, Cuisset JM, Marret S, Drunat S, Faure P, Audebert-Bellanger S, Desguerre I, Flurin V, Grebille AG, Guerrot AM, Journel H, Morin G, Plessis G, Renolleau S, Roume J, Simon-Bouy B, Touraine R, Willems M, Frébourg T, Verspyck E, Saugier-Veber P.
    J Neuromuscul Dis; 2016 Nov 29; 3(4):487-495. PubMed ID: 27911332
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  • 16. [An autopsy case with lower motor neuron disease showing a transient-appearance of anti-GM1 antibody and an improvement of conduction block after gamma-globulin administration].
    Kikuchi H, Kawano Y, Dohura K, Kawamura T, Taniwaki T, Yamada T, Kato M, Iwaki T, Kira J.
    No To Shinkei; 1999 May 29; 51(5):455-64. PubMed ID: 10396755
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  • 17. Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.
    Boylan KB, Cornblath DR.
    Ann Neurol; 1992 Sep 29; 32(3):404-7. PubMed ID: 1416812
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  • 19. [Juvenile muscular atrophy of unilateral upper extremity (Hirayama disease)--half-century progress and establishment since its discovery].
    Hirayama K.
    Brain Nerve; 2008 Jan 29; 60(1):17-29. PubMed ID: 18232329
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