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Journal Abstract Search

235 related items for PubMed ID: 10700541

  • 1. Prenatal onset spinal muscular atrophy.
    MacLeod MJ, Taylor JE, Lunt PW, Mathew CG, Robb SA.
    Eur J Paediatr Neurol; 1999; 3(2):65-72. PubMed ID: 10700541
    [Abstract] [Full Text] [Related]

  • 2. Very severe spinal muscular atrophy (SMA type 0): an expanding clinical phenotype.
    Dubowitz V.
    Eur J Paediatr Neurol; 1999; 3(2):49-51. PubMed ID: 10700538
    [Abstract] [Full Text] [Related]

  • 3. [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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  • 7. Genotype-phenotype studies in infantile spinal muscular atrophy (SMA) type I in Germany: implications for clinical trials and genetic counselling.
    Rudnik-Schöneborn S, Berg C, Zerres K, Betzler C, Grimm T, Eggermann T, Eggermann K, Wirth R, Wirth B, Heller R.
    Clin Genet; 2009 Aug 08; 76(2):168-78. PubMed ID: 19780763
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  • 8. Prenatal diagnosis of spinal muscular atrophy in Chinese by genetic analysis of fetal cells.
    Wu T, Ding XS, Li WL, Yao J, Deng XX.
    Chin Med J (Engl); 2005 Aug 05; 118(15):1274-7. PubMed ID: 16117881
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  • 9. Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system.
    Shaw SW, Cheng PJ, Chang SD, Lin YT, Hung CC, Chen CP, Su YN.
    Acta Obstet Gynecol Scand; 2008 Aug 05; 87(9):960-8. PubMed ID: 18720039
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  • 10. Spinal muscular atrophy: survival pattern and functional status.
    Chung BH, Wong VC, Ip P.
    Pediatrics; 2004 Nov 05; 114(5):e548-53. PubMed ID: 15492357
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  • 11. Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature.
    Haliloglu G, Chattopadhyay A, Skorodis L, Manzur A, Mercuri E, Talim B, Akçören Z, Renda Y, Muntoni F, Topaloğlu H.
    Neuropediatrics; 2002 Dec 05; 33(6):314-9. PubMed ID: 12571787
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  • 13. [Molecular diagnosis of spinal muscular atrophy by multiplex ligation-dependent probe amplification].
    Zeng J, Ke LF, Deng XJ, Cai MY, Tu XD, Lan FH.
    Zhonghua Yi Xue Za Zhi; 2008 Dec 16; 88(46):3262-4. PubMed ID: 19159550
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  • 14. [Diagnostic progress in spinal muscular atrophy].
    Gergont A, Kaciński M, Steczkowska-Klucznik M.
    Przegl Lek; 2001 Dec 16; 58(11):989-91. PubMed ID: 11987841
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  • 15. Prenatal prediction of spinal muscular atrophy by SMN deletion analysis.
    Dhamcharee V, Mutirangura A, Tannirandom Y, Jongpiputvanich S, Romyanan O.
    Southeast Asian J Trop Med Public Health; 1999 Dec 16; 30 Suppl 2():186-7. PubMed ID: 11400766
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  • 16. Prenatal diagnosis of Werdnig-Hoffmann disease in China.
    Feng J, Toshiyuki Y.
    Chin Med J (Engl); 2003 May 16; 116(5):673-5. PubMed ID: 12875676
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  • 17. [Gene diagnosis for spinal muscular atrophy and its application study].
    Cao DH, Ren MH, Lin CK, Cui WT, Ma HW, Wu YY, Jin CL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun 16; 26(3):306-9. PubMed ID: 19504445
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  • 18. Synaptic defects in type I spinal muscular atrophy in human development.
    Martínez-Hernández R, Bernal S, Also-Rallo E, Alías L, Barceló MJ, Hereu M, Esquerda JE, Tizzano EF.
    J Pathol; 2013 Jan 16; 229(1):49-61. PubMed ID: 22847626
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  • 19. Clinical and molecular diagnosis of spinal muscular atrophy.
    Panigrahi I, Kesari A, Phadke SR, Mittal B.
    Neurol India; 2002 Jun 16; 50(2):117-22. PubMed ID: 12134171
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  • 20. [The gene of spinal muscular atrophy localized. Possibilities for prenatal diagnosis].
    Blennow ES, Bui TH, Söderhäll S, Anvret M, Nordenskjöld M.
    Lakartidningen; 1993 Jan 27; 90(4):269-75. PubMed ID: 8433608
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