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Journal Abstract Search

214 related items for PubMed ID: 8232383

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  • 3. Newly recognized congenital myasthenic syndrome associated with high conductance and fast closure of the acetylcholine receptor channel.
    Engel AG, Uchitel OD, Walls TJ, Nagel A, Harper CM, Bodensteiner J.
    Ann Neurol; 1993 Jul; 34(1):38-47. PubMed ID: 7685992
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  • 5. A new myasthenic syndrome with end-plate acetylcholinesterase deficiency, small nerve terminals, and reduced acetylcholine release.
    Engel AG, Lambert EH, Gomez MR.
    Ann Neurol; 1977 Apr; 1(4):315-30. PubMed ID: 214017
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  • 7. Structure-function correlations in myasthenia gravis and a new myasthenic syndrome.
    Engel AG, Lambert EH.
    Electroencephalogr Clin Neurophysiol Suppl; 1978 Apr; (34):469-77. PubMed ID: 220007
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  • 15. Patch-clamp analysis of the properties of acetylcholine receptor channels at the normal human endplate.
    Milone M, Hutchinson DO, Engel AG.
    Muscle Nerve; 1994 Dec; 17(12):1364-9. PubMed ID: 7526207
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  • 16. A newly recognized congenital myasthenic syndrome attributed to a prolonged open time of the acetylcholine-induced ion channel.
    Engel AG, Lambert EH, Mulder DM, Torres CF, Sahashi K, Bertorini TE, Whitaker JN.
    Ann Neurol; 1982 Jun; 11(6):553-69. PubMed ID: 6287911
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  • 17. Novel truncating RAPSN mutations causing congenital myasthenic syndrome responsive to 3,4-diaminopyridine.
    Banwell BL, Ohno K, Sieb JP, Engel AG.
    Neuromuscul Disord; 2004 Mar; 14(3):202-7. PubMed ID: 15036330
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  • 18. Desensitization of mutant acetylcholine receptors in transgenic mice reduces the amplitude of neuromuscular synaptic currents.
    Bhattacharyya BJ, Day JW, Gundeck JE, Leonard S, Wollmann RL, Gomez CM.
    Synapse; 1997 Dec; 27(4):367-77. PubMed ID: 9372559
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