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APPROACH TO PATIENTS WITH NEUROMUSCULAR DISEASE and clinical correlates of anti-neural IgM antibodies in neuropathy associated with IgM monoclonal gammopathy Ann Neurol 1994;36:416 424 Nobile-Orazio E, Latov N, Takatsu M, et al Neuropathy and anti-MAG antibodies without detectable serum M-protein Neurology 1984;34:218 221 Pestronk A, Li F, Bieser K, et al Anti-MAG antibodies: Major effects of antigen purity and antibody crossreactivity on ELISA results and clinical correlation Neurology 1994;44:1131 1137 Patrick J, Lindstrom J Autoimmune response to acetylcholine receptor Science 1973;180:871 872 Kaminski HJ, Sanantilan C, Wolfe GI Antibody testing in neuromuscular disorders, part 2: Neuromuscular junction, hyperexcitability and muscle disorders J Clin Neuromusc Dis 2000:2:96 105 Lindstrom JM, Seybold ME, Lennon VA, Whittingham S, Duane DD Antibody to acetylcholine receptor in myasthenia gravis Prevalence, clinical correlates, and diagnostic value Neurology 1976;26:1054 1059 Vincent A, Newsom-Davis J Acetylcholine receptor antibody as a diagnostic test for myasthenia gravis: Results in 153 validated cases and 2967 diagnostic assays J Neurol Neurosurg Psychiatry 1985, 48:1246 1252 Lanska DJ Diagnosis of thymoma in myasthenics using anti-striated muscle antibodies: Predictive value and gain in diagnostic certainty Neurology 1991;41:520 524 Aarli JA Titin, thymoma, and myasthenia gravis Arch Neurol 2001;58:869 870 Lennon VA Serological diagnosis of myasthenia gravis and the Lambert Eaton myasthenic syndrome In Dekker M (ed) Handbook of Myasthenia Gravis and Myasthenic Syndromes New York, NY: Marcel Dekker, 1994, pp 149 164 Reimers CD, Schedel H, Fleckenstein JL, et al Magnetic resonance imaging of skeletal muscles in idiopathic in ammatory myopathies of adults J Neurol 1994;241:306 314 Cikes N, Momoi M, Williams CL, et al Striational autoantibodies: Quantitative detection by enzyme immunoassay in myasthenia gravis, thymoma and recipients of Dpenicillamine and allogeneic bone marrow Mayo Clin Proc 1988;63:474 481 Burges J, Vincent A, Molennar PC, Newsom-Davis J, Peers C, Wray D Passive transfer of seronegative myasthenia gravis to mice Muscle Nerve 1994;17:1393 1400 Evoli A, Batocchi AP, Lo Monaco M, et al Clinical heterogeneity of seronegative myasthenia gravis Neuromuscul Disord 1996;6:155 161 Hoch W, McConville J, Helms S, Newsom-Davis J, Melms A, Vincent A Autoantibodies to the receptor tyrosine kinase MuSK in patients with myasthenia gravis without acetylcholine receptor antibodies Nat Med 2001;7:365 368 Deymeer F, Gungor-Tuncer O, Yilmaz V, et al Clinical comparison of anti-MuSK- vs anti-AchR-positive and seronegative myasthenia gravis Neurology 2007;68:609 611 Evoli A, Padua L, Monaco ML, et al Clinical correlates with anti-MuSK antibodies in generalized seronegative myasthenia gravis Brain 2003;126:2304 2311
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82 Carpo M, Allaria S, Scarlato G, Nobile-Orazio E Marginally improved detection of GM1 antibodies by Covalink ELISA in multifocal motor neuropathy Neurology 1999;53:2206 2207 83 Freddo L, Yu RK, Latov N, et al Gangliosides GM1 and GD1b are antigens for IgM M-protein in a patient with motor neuron disease Neurology 1986;36:454 458 84 Kinsella LJ, Lange DJ, Trojaborg W, Sadiq SA, Younger DS, Latov N Clinical and electrophysiologic correlates of elevated anti-GM-1 antibody titers Neurology 1994;44:1278 1282 85 Nobile-Orazio E, Cappellari A, Priori A Multifocal motor neuropathy: Current concepts and controversies Muscle Nerve 2005;31:663 680 86 Pestronk A, Chaudhry, Feldman EL, et al Lower motor neuron syndromes de ned by patterns of weakness, nerve conduction abnormalities, and high titres of antiglycolipid antibodies Ann Neurol 1990;27:316 326 87 von Schaik IN, Bossuyt PM, Brand A, Vermeulen M Diagnostic value of GM1 antibodies in motor neuron disorders and neuropathies: A meta-analysis Neurology 1995;45:1570 1577 88 Park JH, Olsen NJ, King L, Jr, et al Use of magnetic resonance imaging and P-31 magnetic resonance spectroscopy to detect and quantify muscle dysfunction in the amyopathic and myopathic variants of dermatomyositis Arthritis Rheum 1995;38:68 77 89 Swash M, Brown MM, Thakkar C CT muscle imaging and the clinical assessment of neuromuscular disease Muscle Nerve 1995;18:708 714 90 Pestronk A, Choksi R Multifocal motor neuropathy Serum IgM anti-GM1 ganglioside antibodies in most patients detected using covalent linkage of GM1 to ELISA plates Neurology 1997;49:1289 1292 91 Carpo M, Pedotti R, Allaria S, et al Clinical presentation and outcome of Guillain Barr and related syndromes e in relation to anti-ganglioside antibodies J Neurol Sci 1999;168:78 84 92 Chiba A, Kusunoki S, Obata H, et al Serum antiGQ1b IgG antibody is associated with ophthalmoplegia in Miller Fisher syndrome and Guillain Barre syndrome: Clinical and immunohistochemical studies Neurology 1993;43:414 417 93 Willison HJ, Veitch J, Paterson G, et al Miller Fisher syndrome is associated with serum antibodies to GQ1b ganglioside J Neurol Neurosurg Psychiatry 1993;56:204 206 94 Yuki N, Sato S, Tsuji S, et al Frequent presence of anti-GQ1b antibody in Fisher s syndrome Neurology 1993;43:414 417 95 Latov N, Sherman WH, Nemni R, et al Plasma-cell dyscrasia and peripheral neuropathy with a monoclonal antibody to peripheral-nerve myelin N Engl J Med 1980;303:618 621 96 Gosselin S, Kyle RA, Dyck PJ Neuropathy associated with monoclonal gammopathy of undetermined signi cance Ann Neurol 1991;30:54 61 97 Katz JS, Saperstein DS, Gronseth G, et al Distal acquired demyelinating symmetric neuropathy Neurology 2000;54:615 620 98 Nobile-Orazio E, Manfredini E, Carpo M, et al Frequency
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