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Journal Abstract Search


127 related items for PubMed ID: 9330889

  • 1. Emery-Dreifuss syndrome.
    Tsuchiya Y, Arahata K.
    Curr Opin Neurol; 1997 Oct; 10(5):421-5. PubMed ID: 9330889
    [Abstract] [Full Text] [Related]

  • 2. Emery-Dreifuss syndrome.
    Emery AE.
    J Med Genet; 1989 Oct; 26(10):637-41. PubMed ID: 2685312
    [Abstract] [Full Text] [Related]

  • 3. X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type).
    Emery AE.
    Clin Genet; 1987 Nov; 32(5):360-7. PubMed ID: 3319295
    [Abstract] [Full Text] [Related]

  • 4. Early onset, autosomal recessive muscular dystrophy with Emery-Dreifuss phenotype and normal emerin expression.
    Taylor J, Sewry CA, Dubowitz V, Muntoni F.
    Neurology; 1998 Oct; 51(4):1116-20. PubMed ID: 9781539
    [Abstract] [Full Text] [Related]

  • 5. [Emery-Dreifuss muscular dystrophy].
    Kubo S, Tsukahara T, Arahata K.
    Nihon Rinsho; 1997 Dec; 55(12):3186-9. PubMed ID: 9436433
    [Abstract] [Full Text] [Related]

  • 6. Cardiac involvement in Emery Dreifuss muscular dystrophy: a case series.
    Buckley AE, Dean J, Mahy IR.
    Heart; 1999 Jul; 82(1):105-8. PubMed ID: 10377322
    [Abstract] [Full Text] [Related]

  • 7. Distinct regions specify the nuclear membrane targeting of emerin, the responsible protein for Emery-Dreifuss muscular dystrophy.
    Tsuchiya Y, Hase A, Ogawa M, Yorifuji H, Arahata K.
    Eur J Biochem; 1999 Feb; 259(3):859-65. PubMed ID: 10092874
    [Abstract] [Full Text] [Related]

  • 8. Emerin and cardiomyopathy in Emery-Dreifuss muscular dystrophy.
    Funakoshi M, Tsuchiya Y, Arahata K.
    Neuromuscul Disord; 1999 Mar; 9(2):108-14. PubMed ID: 10220866
    [Abstract] [Full Text] [Related]

  • 9. Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletion.
    Fujimoto S, Ishikawa T, Saito M, Wada Y, Wada I, Arahata K, Nonaka I.
    Neuropediatrics; 1999 Jun; 30(3):161-3. PubMed ID: 10480214
    [Abstract] [Full Text] [Related]

  • 10. [Hauptmann-Thannhauser muscular dystrophy and differential diagnosis of myopathies associated with contractures].
    Hanisch F, Neudecker S, Wehnert M, Zierz S.
    Nervenarzt; 2002 Oct; 73(10):1004-11. PubMed ID: 12376891
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  • 13. Emery-Dreifuss muscular dystrophy and other related disorders.
    Emery AE.
    Br Med Bull; 1989 Jul; 45(3):772-87. PubMed ID: 2688828
    [Abstract] [Full Text] [Related]

  • 14. Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy.
    Muntoni F, Lichtarowicz-Krynska EJ, Sewry CA, Manilal S, Recan D, Llense S, Taylor J, Morris GE, Dubowitz V.
    Neuromuscul Disord; 1998 Apr; 8(2):72-6. PubMed ID: 9608559
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  • 16. Changes at P183 of emerin weaken its protein-protein interactions resulting in X-linked Emery-Dreifuss muscular dystrophy.
    Ellis JA, Yates JR, Kendrick-Jones J, Brown CA.
    Hum Genet; 1999 Mar; 104(3):262-8. PubMed ID: 10323252
    [Abstract] [Full Text] [Related]

  • 17. [Dominant autosomal humeroperoneal syndrome with early contractures and cardiomyopathy (Emery-Dreifuss syndrome)].
    Baur X, Witt TN, Pongratz D, Gokel M, Rosenbeiger P, Steinbeck G.
    Klin Wochenschr; 1987 Aug 03; 65(15):738-45. PubMed ID: 3626437
    [Abstract] [Full Text] [Related]

  • 18. Mutation analysis in Emery-Dreifuss muscular dystrophy.
    Nevo Y, Al-Lozi M, Parsadanian AS, Elliott JL, Connolly AM, Pestronk A.
    Pediatr Neurol; 1999 Jul 03; 21(1):456-9. PubMed ID: 10428430
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