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Journal Abstract Search

177 related items for PubMed ID: 1641139

  • 1. 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; 42(8):1477-80. PubMed ID: 1641139
    [Abstract] [Full Text] [Related]

  • 2. Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.
    Boylan KB, Cornblath DR.
    Ann Neurol; 1992 Sep; 32(3):404-7. PubMed ID: 1416812
    [Abstract] [Full Text] [Related]

  • 3. The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13.
    Brunialti AL, Poirier C, Schmalbruch H, Guénet JL.
    Genomics; 1995 Sep 01; 29(1):131-5. PubMed ID: 8530062
    [Abstract] [Full Text] [Related]

  • 4. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.
    Gilliam TC, Brzustowicz LM, Castilla LH, Lehner T, Penchaszadeh GK, Daniels RJ, Byth BC, Knowles J, Hislop JE, Shapira Y.
    Nature; 1990 Jun 28; 345(6278):823-5. PubMed ID: 1972783
    [Abstract] [Full Text] [Related]

  • 5. Infantile progressive spinal muscular atrophy with ophthalmoplegia and pyramidal symptoms.
    Hamano K, Tsukamoto H, Yazawa T, Yoshimura M, Takita H.
    Pediatr Neurol; 1994 Jun 28; 10(4):320-4. PubMed ID: 8068160
    [Abstract] [Full Text] [Related]

  • 6. [Indirect molecular-genetic family study and prenatal diagnosis of infantile spinal muscular atrophy].
    Heber U, Müller CR.
    Klin Padiatr; 1994 Jun 28; 206(1):30-5. PubMed ID: 8152204
    [Abstract] [Full Text] [Related]

  • 7. Ultrastructural analysis and TUNEL demonstrate motor neuron apoptosis in Werdnig-Hoffmann disease.
    Simic G, Seso-Simic D, Lucassen PJ, Islam A, Krsnik Z, Cviko A, Jelasic D, Barisic N, Winblad B, Kostovic I, Kruslin B.
    J Neuropathol Exp Neurol; 2000 May 28; 59(5):398-407. PubMed ID: 10888370
    [Abstract] [Full Text] [Related]

  • 8. Controversy over Werdnig-Hoffmann disease and multiple system atrophy.
    Chou SM.
    Curr Opin Neurol; 1993 Dec 28; 6(6):861-4. PubMed ID: 8293160
    [No Abstract] [Full Text] [Related]

  • 9. Spinal muscular atrophy.
    Melki J.
    Curr Opin Neurol; 1997 Oct 28; 10(5):381-5. PubMed ID: 9330883
    [Abstract] [Full Text] [Related]

  • 10. 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 28; 23(2):199-204. PubMed ID: 18263757
    [Abstract] [Full Text] [Related]

  • 11. X-linked infantile spinal muscular atrophy.
    Greenberg F, Fenolio KR, Hejtmancik JF, Armstrong D, Willis JK, Shapira E, Huntington HW, Haun RL.
    Am J Dis Child; 1988 Feb 28; 142(2):217-9. PubMed ID: 3341327
    [Abstract] [Full Text] [Related]

  • 12. Migrating atelectasis in Werdnig-Hoffmann disease: pulmonary manifestations in two cases of spinal muscular atrophy type 1.
    Leistikow EA, Jones NE, Josephson KD, de Sierra TM, Costakos DT, Sprague D, Gorch DH, Asonye UO.
    Pediatr Pulmonol; 1999 Aug 28; 28(2):149-53. PubMed ID: 10423316
    [Abstract] [Full Text] [Related]

  • 13. Neonatal spinal muscular atrophy with multiple contractures, bone fractures, respiratory insufficiency and 5q13 deletion.
    García-Cabezas MA, García-Alix A, Martín Y, Gutiérrez M, Hernández C, Rodríguez JI, Morales C.
    Acta Neuropathol; 2004 May 28; 107(5):475-8. PubMed ID: 14968368
    [Abstract] [Full Text] [Related]

  • 14. [Spinal muscular atrophy in young infants].
    Smit LM, Hageman EG.
    Tijdschr Kindergeneeskd; 1989 Jun 28; 57(3):102-6. PubMed ID: 2799798
    [Abstract] [Full Text] [Related]

  • 15. Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophy.
    Omran H, Ketelsen UP, Heinen F, Sauer M, Rudnik-Schöneborn S, Wirth B, Zerres K, Kratzer W, Korinthenberg R.
    J Child Neurol; 1998 Jul 28; 13(7):327-31. PubMed ID: 9701481
    [Abstract] [Full Text] [Related]

  • 16. [Spinal muscular atrophy : Time for newborn screening?].
    Vill K, Blaschek A, Schara U, Kölbel H, Hohenfellner K, Harms E, Olgemöller B, Walter MC, Müller-Felber W.
    Nervenarzt; 2017 Dec 28; 88(12):1358-1366. PubMed ID: 29101527
    [Abstract] [Full Text] [Related]

  • 17. Infantile spinal muscular atrophy (SMA) and multiple congenital bone fractures in sibs: a lethal new syndrome.
    Borochowitz Z, Glick B, Blazer S.
    J Med Genet; 1991 May 28; 28(5):345-8. PubMed ID: 1865475
    [Abstract] [Full Text] [Related]

  • 18. [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
    [No Abstract] [Full Text] [Related]

  • 19. Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family.
    Appelbaum JS, Roos RP.
    Muscle Nerve; 1993 Dec 30; 16(12):1416. PubMed ID: 8232401
    [No Abstract] [Full Text] [Related]

  • 20. Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degeneration.
    Rudnik-Schöneborn S, Wirth B, Röhrig D, Saule H, Zerres K.
    Neuromuscul Disord; 1995 Jan 30; 5(1):19-23. PubMed ID: 7719136
    [Abstract] [Full Text] [Related]

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