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Volumn 4, Issue 2, 2007, Pages 252-257

Correction to: The Therapy of Congenital Myasthenic Syndromes (Neurotherapeutics, (2007), 4, 2, (252-257), 10.1016/j.nurt.2007.01.001);The Therapy of Congenital Myasthenic Syndromes

Author keywords

3,4 diaminopyridine; acetylcholine receptor; acetylcholinesterase; choline acetyltransferase; cholinesterase inhibitors; Congenital myasthenic syndromes; Dok 7; fluoxetine; MuSK; quinidine; rapsyn

Indexed keywords

3,4 DIAMINOPYRIDINE; ACETYLCHOLINE; ANTIARRHYTHMIC AGENT; CHOLINE ACETYLTRANSFERASE; CHOLINERGIC RECEPTOR; CHOLINESTERASE INHIBITOR; CIMETIDINE; CODEINE; DIGOXIN; EPHEDRINE; EPHEDRINE SULFATE; FLUOXETINE; NEOSTIGMINE METHYL SULFATE; PREDNISONE; PROTEIN DOK7; PYRIDOSTIGMINE; QUINIDINE SULFATE; RAPSYN; REGULATOR PROTEIN; TRICYCLIC ANTIDEPRESSANT AGENT; UNCLASSIFIED DRUG; VERAPAMIL; WARFARIN;

EID: 33947497536     PISSN: 19337213     EISSN: 18787479     Source Type: Journal    
DOI: 10.1007/s13311-018-00672-6     Document Type: Erratum
Times cited : (99)

References (46)
  • 1
    • 0002321039 scopus 로고
    • Vertebrate neuromuscular junctions: general morphology, molecular organization, and functional consequences
    • Salpeter M.M. (Ed), Wiley, New York
    • Salpeter M.M. Vertebrate neuromuscular junctions: general morphology, molecular organization, and functional consequences. In: Salpeter M.M. (Ed). The vertebrate neuromuscular junction (1987), Wiley, New York 1-54
    • (1987) The vertebrate neuromuscular junction , pp. 1-54
    • Salpeter, M.M.1
  • 2
    • 0024708031 scopus 로고
    • Distribution of Na+ channels and ankyrin in neuromuscular junctions is complementary to that of acetylcholine receptors and the 43 kd protein
    • Flucher B.E., and Daniels M.P. Distribution of Na+ channels and ankyrin in neuromuscular junctions is complementary to that of acetylcholine receptors and the 43 kd protein. Neuron 3 (1989) 163-175
    • (1989) Neuron , vol.3 , pp. 163-175
    • Flucher, B.E.1    Daniels, M.P.2
  • 3
    • 0030006021 scopus 로고    scopus 로고
    • Sodium channel slow inactivation and the distribution of sodium channels on skeletal muscle fibres enable the performance properties of different skeletal muscle fiber types
    • Ruff R.L. Sodium channel slow inactivation and the distribution of sodium channels on skeletal muscle fibres enable the performance properties of different skeletal muscle fiber types. Acta Physiol Scand 156 (1996) 159-168
    • (1996) Acta Physiol Scand , vol.156 , pp. 159-168
    • Ruff, R.L.1
  • 4
    • 0028595963 scopus 로고
    • Amplification of neuromuscular transmission by postjunctional folds
    • Martin A.R. Amplification of neuromuscular transmission by postjunctional folds. Proc R Soc Lond B Biol Sci 258 (1994) 321-326
    • (1994) Proc R Soc Lond B Biol Sci , vol.258 , pp. 321-326
    • Martin, A.R.1
  • 5
    • 0035084963 scopus 로고    scopus 로고
    • Safety factor at the neuromuscular junction
    • Wood S.J., and Slater C.P. Safety factor at the neuromuscular junction. Prog Neurobiol 64 (2001) 393-429
    • (2001) Prog Neurobiol , vol.64 , pp. 393-429
    • Wood, S.J.1    Slater, C.P.2
  • 6
    • 10144229353 scopus 로고    scopus 로고
    • New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome
    • Engel A.G., Ohno K., Milone M., et al. New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome. Hum Mol Genet 5 (1996) 1217-1227
    • (1996) Hum Mol Genet , vol.5 , pp. 1217-1227
    • Engel, A.G.1    Ohno, K.2    Milone, M.3
  • 7
    • 0035852681 scopus 로고    scopus 로고
    • Choline acetyltransferase mutations cause myasthenic syndrome associated with episodic apnea in humans
    • Ohno K., Tsujino A., Brengman J.M., et al. Choline acetyltransferase mutations cause myasthenic syndrome associated with episodic apnea in humans. Proc Natl Acad Sci U S A 98 (2001) 2017-2022
    • (2001) Proc Natl Acad Sci U S A , vol.98 , pp. 2017-2022
    • Ohno, K.1    Tsujino, A.2    Brengman, J.M.3
  • 8
    • 0027200547 scopus 로고
    • The investigation of congenital myasthenic syndromes
    • Engel A.G. The investigation of congenital myasthenic syndromes. Ann NY Acad Sci 681 (1993) 425-434
    • (1993) Ann NY Acad Sci , vol.681 , pp. 425-434
    • Engel, A.G.1
  • 9
    • 0032103142 scopus 로고    scopus 로고
    • Quinidine normalizes the open duration of slow-channel mutants of the acetylcholine receptor
    • Fukudome T., Ohno K., Brengman J.M., and Engel A.G. Quinidine normalizes the open duration of slow-channel mutants of the acetylcholine receptor. Neuroreport 9 (1998) 1907-1911
    • (1998) Neuroreport , vol.9 , pp. 1907-1911
    • Fukudome, T.1    Ohno, K.2    Brengman, J.M.3    Engel, A.G.4
  • 10
    • 0038476135 scopus 로고    scopus 로고
    • Treatment of slow channel congenital myasthenic syndrome with fluoxetine
    • Harper C.M., Fukudome T., and Engel A.G. Treatment of slow channel congenital myasthenic syndrome with fluoxetine. Neurology 60 (2003) 170-173
    • (2003) Neurology , vol.60 , pp. 170-173
    • Harper, C.M.1    Fukudome, T.2    Engel, A.G.3
  • 11
    • 0032483003 scopus 로고    scopus 로고
    • Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme
    • Ohno K., Brengman J.M., Tsujino A., and Engel A.G. Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme. Proc Natl Acad Sci U S A 95 (1998) 9654-9659
    • (1998) Proc Natl Acad Sci U S A , vol.95 , pp. 9654-9659
    • Ohno, K.1    Brengman, J.M.2    Tsujino, A.3    Engel, A.G.4
  • 12
    • 8244225989 scopus 로고    scopus 로고
    • Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor e subunit gene: identification and functional characterization of six new mutations
    • Ohno K., Quiram P.A., Milone M., et al. Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor e subunit gene: identification and functional characterization of six new mutations. Hum Mol Genet 6 (1997) 753-766
    • (1997) Hum Mol Genet , vol.6 , pp. 753-766
    • Ohno, K.1    Quiram, P.A.2    Milone, M.3
  • 13
    • 0036206747 scopus 로고    scopus 로고
    • Rapsyn mutations in humans cause endplate acetylcholine receptor deficiency and myasthenic syndrome
    • Ohno K., Engel A.G., Shen X.M., et al. Rapsyn mutations in humans cause endplate acetylcholine receptor deficiency and myasthenic syndrome. Am J Hum Genet 70 (2002) 875-885
    • (2002) Am J Hum Genet , vol.70 , pp. 875-885
    • Ohno, K.1    Engel, A.G.2    Shen, X.M.3
  • 14
    • 19944396127 scopus 로고    scopus 로고
    • MUSK, a new target for mutations causing congenital myasthenic syndrome
    • Chevessier F., Faraut B., Ravel-Chapuis A., et al. MUSK, a new target for mutations causing congenital myasthenic syndrome. Hum Mol Genet 13 (2004) 3229-3240
    • (2004) Hum Mol Genet , vol.13 , pp. 3229-3240
    • Chevessier, F.1    Faraut, B.2    Ravel-Chapuis, A.3
  • 15
    • 33749068357 scopus 로고    scopus 로고
    • Dok-7 mutations underlie a neuromuscular junction synaptopathy
    • Beeson D., Higuchi O., Palace J., et al. Dok-7 mutations underlie a neuromuscular junction synaptopathy. Science 313 (2006) 1975-1978
    • (2006) Science , vol.313 , pp. 1975-1978
    • Beeson, D.1    Higuchi, O.2    Palace, J.3
  • 16
    • 0031829201 scopus 로고    scopus 로고
    • Myasthenic syndromes in Turkish kinships due to mutations in the acetylcholine receptor
    • Ohno K., Anlar B., Ozdirim E., Brengman J.M., DeBleecker J.L., and Engel A.G. Myasthenic syndromes in Turkish kinships due to mutations in the acetylcholine receptor. Ann Neurol 44 (1998) 234-241
    • (1998) Ann Neurol , vol.44 , pp. 234-241
    • Ohno, K.1    Anlar, B.2    Ozdirim, E.3    Brengman, J.M.4    DeBleecker, J.L.5    Engel, A.G.6
  • 17
    • 20244383427 scopus 로고    scopus 로고
    • Congenital myasthenic syndromes linked to chromosome 17p are caused by defects in acetylcholine receptor e subunit gene
    • Middleton L., Ohno K., Christodoulou K., and Sine S.M. Congenital myasthenic syndromes linked to chromosome 17p are caused by defects in acetylcholine receptor e subunit gene. Neurology 53 (1999) 1076-1082
    • (1999) Neurology , vol.53 , pp. 1076-1082
    • Middleton, L.1    Ohno, K.2    Christodoulou, K.3    Sine, S.M.4
  • 18
    • 0037162345 scopus 로고    scopus 로고
    • Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes
    • Croxen R., Hatton C., Shelley C., et al. Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes. Neurology 59 (2002) 162-168
    • (2002) Neurology , vol.59 , pp. 162-168
    • Croxen, R.1    Hatton, C.2    Shelley, C.3
  • 19
    • 33947531963 scopus 로고
    • Kinetic analysis of a large facilitatory action of 4-aminopyridine on the motor nerve terminal of the neuromuscular junction
    • Maeno T. Kinetic analysis of a large facilitatory action of 4-aminopyridine on the motor nerve terminal of the neuromuscular junction. Proc Jpn Acad 56 (1980) 241-245
    • (1980) Proc Jpn Acad , vol.56 , pp. 241-245
    • Maeno, T.1
  • 20
    • 0024350963 scopus 로고
    • The effects of 4-aminopyridine and tetraethylammonium on the kinetics of transmitter release at the mammalian neuromuscular synapse
    • Saint D.A. The effects of 4-aminopyridine and tetraethylammonium on the kinetics of transmitter release at the mammalian neuromuscular synapse. Can J Physiol Pharmacol 67 (1989) 1045-1050
    • (1989) Can J Physiol Pharmacol , vol.67 , pp. 1045-1050
    • Saint, D.A.1
  • 21
    • 0024367939 scopus 로고
    • 3,4-Diaminopyridine in the treatment of Lambert-Eaton myasthenic syndrome
    • McEvoy K.M., Windebank A.J., Daube J.R., and Low P.A. 3,4-Diaminopyridine in the treatment of Lambert-Eaton myasthenic syndrome. N Engl J Med 321 (1989) 1567-1571
    • (1989) N Engl J Med , vol.321 , pp. 1567-1571
    • McEvoy, K.M.1    Windebank, A.J.2    Daube, J.R.3    Low, P.A.4
  • 22
    • 0027199048 scopus 로고
    • 3,4-diaminopyridine in Lambert-Eaton myasthenic syndrome and myasthenia gravis
    • Sanders D.B., Howard Jr. J.F., and Massey J.M. 3,4-diaminopyridine in Lambert-Eaton myasthenic syndrome and myasthenia gravis. Ann NY Acad Sci 681 (1993) 588-590
    • (1993) Ann NY Acad Sci , vol.681 , pp. 588-590
    • Sanders, D.B.1    Howard Jr., J.F.2    Massey, J.M.3
  • 23
    • 0001057062 scopus 로고    scopus 로고
    • Treatment of 31 congenital myasthenic syndrome patients with 3,4-diaminopyridine
    • Harper C.M., and Engel A.G. Treatment of 31 congenital myasthenic syndrome patients with 3,4-diaminopyridine. Neurology 54 suppl 3 (2000) A395
    • (2000) Neurology , vol.54 , Issue.SUPPL. 3
    • Harper, C.M.1    Engel, A.G.2
  • 24
    • 0026322540 scopus 로고
    • 3,4-diaminopyridine in the treatment of congenital (hereditary) myasthenia
    • Palace J., Wiles C.M., and Newsom-Davis J. 3,4-diaminopyridine in the treatment of congenital (hereditary) myasthenia. J Neurol Neurosurg Psychiatry 54 (1991) 1069-1072
    • (1991) J Neurol Neurosurg Psychiatry , vol.54 , pp. 1069-1072
    • Palace, J.1    Wiles, C.M.2    Newsom-Davis, J.3
  • 25
    • 0029827473 scopus 로고    scopus 로고
    • 3,4-diaminopyridine in childhood myasthenia: double blind, placebo controlled trial
    • Anlar B., Varli K., Ozdirim E., and Ertan M. 3,4-diaminopyridine in childhood myasthenia: double blind, placebo controlled trial. J Child Neurol 11 (1996) 458-461
    • (1996) J Child Neurol , vol.11 , pp. 458-461
    • Anlar, B.1    Varli, K.2    Ozdirim, E.3    Ertan, M.4
  • 26
    • 0029807971 scopus 로고    scopus 로고
    • End-plate acetylcholine receptor deficiency due to nonsense mutations in the e subunit
    • Engel A.G., Ohno K., Bouzat C., Sine S.M., and Griggs R.G. End-plate acetylcholine receptor deficiency due to nonsense mutations in the e subunit. Ann Neurol 40 (1996) 810-817
    • (1996) Ann Neurol , vol.40 , pp. 810-817
    • Engel, A.G.1    Ohno, K.2    Bouzat, C.3    Sine, S.M.4    Griggs, R.G.5
  • 27
    • 0037530441 scopus 로고    scopus 로고
    • Sleuthing molecular targets for neurological diseases at the neuromuscular junction
    • Engel A.G., Ohno K., and Sine S.M. Sleuthing molecular targets for neurological diseases at the neuromuscular junction. Nat Rev Neurosci 4 (2003) 339-352
    • (2003) Nat Rev Neurosci , vol.4 , pp. 339-352
    • Engel, A.G.1    Ohno, K.2    Sine, S.M.3
  • 28
    • 0031749640 scopus 로고    scopus 로고
    • Quinidine sulfate therapy for the slow-channel congenital myasthenic syndrome
    • Harper C.M., and Engel A.G. Quinidine sulfate therapy for the slow-channel congenital myasthenic syndrome. Ann Neurol 43 (1998) 480-484
    • (1998) Ann Neurol , vol.43 , pp. 480-484
    • Harper, C.M.1    Engel, A.G.2
  • 29
    • 85080317870 scopus 로고
    • American Medical Association, Milwaukee, WI
    • Drug Evaluations Annual. 7th ed. (1995), American Medical Association, Milwaukee, WI 677-679
    • (1995) Drug Evaluations Annual. 7th ed. , pp. 677-679
  • 30
    • 85080463811 scopus 로고
    • American Medical Association, Milwaukee, WI
    • Drug Evaluations Annual. 7th ed. (1995), American Medical Association, Milwaukee, WI 310-311
    • (1995) Drug Evaluations Annual. 7th ed. , pp. 310-311
  • 31
    • 14744285328 scopus 로고    scopus 로고
    • Are the SSRIs and atypical antidepressants safe and effective for children and adolescents?
    • Whittington C.J., Kendall T., and Pilling S. Are the SSRIs and atypical antidepressants safe and effective for children and adolescents?. Curr Opin Psychiatry 18 (2005) 21-25
    • (2005) Curr Opin Psychiatry , vol.18 , pp. 21-25
    • Whittington, C.J.1    Kendall, T.2    Pilling, S.3
  • 32
    • 33748636892 scopus 로고    scopus 로고
    • Efficacy of selective serotonin reuptake inhibitor treatment in children and adolescents
    • Bailly D. Efficacy of selective serotonin reuptake inhibitor treatment in children and adolescents. Presse Med 35 (2006) 1293-1302
    • (2006) Presse Med , vol.35 , pp. 1293-1302
    • Bailly, D.1
  • 33
    • 0002622227 scopus 로고    scopus 로고
    • Congenital myasthenic syndromes
    • Engel A.G. (Ed), Oxford University Press, New York
    • Engel A.G., Ohno K., and Sine S.M. Congenital myasthenic syndromes. In: Engel A.G. (Ed). Myasthenia gravis and myasthenic disorders (1999), Oxford University Press, New York 251-297
    • (1999) Myasthenia gravis and myasthenic disorders , pp. 251-297
    • Engel, A.G.1    Ohno, K.2    Sine, S.M.3
  • 34
    • 22044438577 scopus 로고    scopus 로고
    • Congenital endplate acetylcholinesterase deficiency responsive to ephedrine
    • Bestue-Cardiel M., Saenz de Cabezon-Alvarez A., Capablo-Liesa J.L., et al. Congenital endplate acetylcholinesterase deficiency responsive to ephedrine. Neurology 65 (2005) 144-146
    • (2005) Neurology , vol.65 , pp. 144-146
    • Bestue-Cardiel, M.1    Saenz de Cabezon-Alvarez, A.2    Capablo-Liesa, J.L.3
  • 35
    • 0027301105 scopus 로고
    • Congenital endplate acetylcholinesterase deficiency
    • Hutchinson D.O., Walls T.J., Nakano S., et al. Congenital endplate acetylcholinesterase deficiency. Brain 116 (1993) 633-653
    • (1993) Brain , vol.116 , pp. 633-653
    • Hutchinson, D.O.1    Walls, T.J.2    Nakano, S.3
  • 36
    • 0029681791 scopus 로고    scopus 로고
    • Treatment of congenital endplate acetylcholinesterase deficiency by neuromuscular blockade
    • Breningstall G.N., Kurachek S.C., Fugate J.H., and Engel A.G. Treatment of congenital endplate acetylcholinesterase deficiency by neuromuscular blockade. J Child Neurol 11 (1996) 345-346
    • (1996) J Child Neurol , vol.11 , pp. 345-346
    • Breningstall, G.N.1    Kurachek, S.C.2    Fugate, J.H.3    Engel, A.G.4
  • 37
    • 10744220964 scopus 로고    scopus 로고
    • Rapsyn mutations in hereditary myasthenia: distinct early- and late-onset phenotypes
    • Burke G., Cossins J., Maxwell S., et al. Rapsyn mutations in hereditary myasthenia: distinct early- and late-onset phenotypes. Neurology 61 (2003) 826-828
    • (2003) Neurology , vol.61 , pp. 826-828
    • Burke, G.1    Cossins, J.2    Maxwell, S.3
  • 38
    • 1242316360 scopus 로고    scopus 로고
    • Novel truncating RAPSN mutation causing congenital myasthenic syndrome responsive to 3,4-diaminopyridine
    • Banwell B.L., Ohno K., Sieb J.P., and Engel A.G. Novel truncating RAPSN mutation causing congenital myasthenic syndrome responsive to 3,4-diaminopyridine. Neuromuscul Disord 14 (2004) 202-207
    • (2004) Neuromuscul Disord , vol.14 , pp. 202-207
    • Banwell, B.L.1    Ohno, K.2    Sieb, J.P.3    Engel, A.G.4
  • 39
    • 33745495950 scopus 로고    scopus 로고
    • The muscle protein Dok-7 is essential for neuromuscular synaptogenesis
    • Okada K., Inoue A., Okada M., et al. The muscle protein Dok-7 is essential for neuromuscular synaptogenesis. Science 312 (2006) 1802-1805
    • (2006) Science , vol.312 , pp. 1802-1805
    • Okada, K.1    Inoue, A.2    Okada, M.3
  • 40
    • 33747883025 scopus 로고    scopus 로고
    • Pre- and postsynaptic abnormalities associated with impaired neuromuscular transmission in a group of patients with 'limb-girdle myasthenia'
    • Slater C.R., Fawcett P.R.W., Walls T.J., et al. Pre- and postsynaptic abnormalities associated with impaired neuromuscular transmission in a group of patients with 'limb-girdle myasthenia'. Brain 129 (2006) 2061-2076
    • (2006) Brain , vol.129 , pp. 2061-2076
    • Slater, C.R.1    Fawcett, P.R.W.2    Walls, T.J.3
  • 41
    • 0027216425 scopus 로고
    • Congenital myasthenic syndrome associated with paucity of synaptic vesicles and reduced quantal release
    • Walls T.J., Engel A.G., Nagel A.S., Harper C.M., and Trastek V.F. Congenital myasthenic syndrome associated with paucity of synaptic vesicles and reduced quantal release. Ann N Y Acad Sci 681 (1993) 461-468
    • (1993) Ann N Y Acad Sci , vol.681 , pp. 461-468
    • Walls, T.J.1    Engel, A.G.2    Nagel, A.S.3    Harper, C.M.4    Trastek, V.F.5
  • 42
    • 0034643865 scopus 로고    scopus 로고
    • Lambert-Eaton myasthenic syndrome: electrodiagnostic findings and response to treatment
    • Tim R.W., Massey J.M., and Sanders D.B. Lambert-Eaton myasthenic syndrome: electrodiagnostic findings and response to treatment. Neurology 54 (2000) 2176-2178
    • (2000) Neurology , vol.54 , pp. 2176-2178
    • Tim, R.W.1    Massey, J.M.2    Sanders, D.B.3
  • 44
    • 0037794423 scopus 로고    scopus 로고
    • Myasthenic syndrome caused by mutation of the SCN4A sodium channel
    • Tsujino A., Maertens C., Ohno K., et al. Myasthenic syndrome caused by mutation of the SCN4A sodium channel. Proc Natl Acad Sci U S A 100 (2003) 7377-7382
    • (2003) Proc Natl Acad Sci U S A , vol.100 , pp. 7377-7382
    • Tsujino, A.1    Maertens, C.2    Ohno, K.3
  • 45
    • 0020047892 scopus 로고
    • A newly recognized congenital myasthenic syndrome attributed to a prolonged open time of the acetylcholine-induced ion channel
    • Engel A.G., Lambert E.H., Mulder D.M., et al. A newly recognized congenital myasthenic syndrome attributed to a prolonged open time of the acetylcholine-induced ion channel. Ann Neurol 11 (1982) 553-569
    • (1982) Ann Neurol , vol.11 , pp. 553-569
    • Engel, A.G.1    Lambert, E.H.2    Mulder, D.M.3
  • 46
    • 0036310759 scopus 로고    scopus 로고
    • Congenital myasthenic syndrome associated with episodic apnea and sudden infant death
    • Byring R.F., Pihko H., Tsujino A., et al. Congenital myasthenic syndrome associated with episodic apnea and sudden infant death. Neuromuscul Disord 12 (2002) 548-553
    • (2002) Neuromuscul Disord , vol.12 , pp. 548-553
    • Byring, R.F.1    Pihko, H.2    Tsujino, A.3


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