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Volumn 17, Issue 6, 2010, Pages 767-773

EFNS guidelines on the diagnostic approach to pauci- or asymptomatic hyperCKemia

Author keywords

Asymptomatic; HyperC Kemia; Investigation; Pauci symptomatic

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT; COLCHICINE; CREATINE KINASE; FIBRIC ACID DERIVATIVE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; ISOTRETINOIN; NEUROLEPTIC AGENT; ZIDOVUDINE;

EID: 77952491243     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2010.03012.x     Document Type: Review
Times cited : (154)

References (34)
  • 2
    • 58249092064 scopus 로고    scopus 로고
    • Should high creatine kinase discourage the initiation or continuance of statins for the treatment of hypercholesterolemia?
    • Glueck CJ, Rawal B, Khan NA, Yeramaneni S, Goldenberg N, Wang P. Should high creatine kinase discourage the initiation or continuance of statins for the treatment of hypercholesterolemia? Metabolism 2009 58 : 233 238.
    • (2009) Metabolism , vol.58 , pp. 233-238
    • Glueck, C.J.1    Rawal, B.2    Khan, N.A.3    Yeramaneni, S.4    Goldenberg, N.5    Wang, P.6
  • 3
    • 65649154464 scopus 로고    scopus 로고
    • Effect of newly proposed CK reference limits on neuromuscular diagnosis
    • Nardin RA, Zarrin AR, Horowitz GL, Tarulli AW. Effect of newly proposed CK reference limits on neuromuscular diagnosis. Muscle Nerve 2009 39 : 494 497.
    • (2009) Muscle Nerve , vol.39 , pp. 494-497
    • Nardin, R.A.1    Zarrin, A.R.2    Horowitz, G.L.3    Tarulli, A.W.4
  • 4
    • 34548784368 scopus 로고    scopus 로고
    • Distribution of creatine kinase in the general population: Implications for statin therapy
    • Brewster LM, Mairuhu G, Sturk A, van Montfrans GA. Distribution of creatine kinase in the general population: implications for statin therapy. Am Heart J 2007 154 : 655 661.
    • (2007) Am Heart J , vol.154 , pp. 655-661
    • Brewster, L.M.1    Mairuhu, G.2    Sturk, A.3    Van Montfrans, G.A.4
  • 5
    • 37849189496 scopus 로고    scopus 로고
    • High plasma creatine kinase: Review of the literature and proposal for a diagnostic algorithm
    • Morandi L, Angelini C, Prelle A, et al. High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm. Neurol Sci 2006 27 : 303 311.
    • (2006) Neurol Sci , vol.27 , pp. 303-311
    • Morandi, L.1    Angelini, C.2    Prelle, A.3
  • 6
    • 4644249308 scopus 로고    scopus 로고
    • Guidance for the preparation of neurological management guidelines by EFNS scientific task forces - Revised recommendations 2004
    • Brainin M, Barnes M, Baron JC, et al. Guidance for the preparation of neurological management guidelines by EFNS scientific task forces - revised recommendations 2004. Eur J Neurol 2004 11 : 577 581.
    • (2004) Eur J Neurol , vol.11 , pp. 577-581
    • Brainin, M.1    Barnes, M.2    Baron, J.C.3
  • 7
    • 77952494654 scopus 로고
    • Approaches to the membrane theory of Duchenne muscular dystrophy
    • Angelini, C. Danielli, G.A. Fontanari, D. eds., Muscular Dystrophy Research: Advances and New Trends, Amsterdam
    • Rowland LPWJ, Cerri C, DiMauro S, Miranda A. Approaches to the membrane theory of Duchenne muscular dystrophy. In : Angelini C, Danielli GA, Fontanari D, eds. Muscular Dystrophy Research: Advances and New Trends, Amsterdam. Excerpta Med 1980 3 13.
    • (1980) Excerpta Med , pp. 3-13
    • Lpwj, R.1    Cerri, C.2    Dimauro, S.3    Miranda, A.4
  • 8
    • 33744951413 scopus 로고    scopus 로고
    • Familial idiopathic hyper-CK-emia: An underrecognized condition
    • Capasso M, De Angelis MV, Di Muzio A, et al. Familial idiopathic hyper-CK-emia: an underrecognized condition. Muscle Nerve 2006 33 : 760 765.
    • (2006) Muscle Nerve , vol.33 , pp. 760-765
    • Capasso, M.1    De Angelis, M.V.2    Di Muzio, A.3
  • 9
    • 18344373838 scopus 로고    scopus 로고
    • Retrospective study of a large population of patients with asymptomatic or minimally symptomatic raised serum creatine kinase levels
    • Prelle A, Tancredi L, Sciacco M, et al. Retrospective study of a large population of patients with asymptomatic or minimally symptomatic raised serum creatine kinase levels. J Neurol 2002 249 : 305 311.
    • (2002) J Neurol , vol.249 , pp. 305-311
    • Prelle, A.1    Tancredi, L.2    Sciacco, M.3
  • 10
    • 0037311248 scopus 로고    scopus 로고
    • Muscle biopsy in the evaluation of patients with modestly elevated creatine kinase levels
    • Simmons Z, Peterlin BL, Boyer PJ, Towfighi J. Muscle biopsy in the evaluation of patients with modestly elevated creatine kinase levels. Muscle Nerve 2003 27 : 242 244.
    • (2003) Muscle Nerve , vol.27 , pp. 242-244
    • Simmons, Z.1    Peterlin, B.L.2    Boyer, P.J.3    Towfighi, J.4
  • 12
    • 33745424580 scopus 로고    scopus 로고
    • Diagnostic evaluation of clinically normal subjects with chronic hyperCKemia
    • Fernandez C, de Paula AM, Figarella-Branger D, et al. Diagnostic evaluation of clinically normal subjects with chronic hyperCKemia. Neurology 2006 66 : 1585 1587.
    • (2006) Neurology , vol.66 , pp. 1585-1587
    • Fernandez, C.1    De Paula, A.M.2    Figarella-Branger, D.3
  • 13
    • 33846265671 scopus 로고    scopus 로고
    • The role of muscle biopsy in investigating isolated muscle pain
    • Filosto M, Tonin P, Vattemi G, et al. The role of muscle biopsy in investigating isolated muscle pain. Neurology 2007 68 : 181 186.
    • (2007) Neurology , vol.68 , pp. 181-186
    • Filosto, M.1    Tonin, P.2    Vattemi, G.3
  • 14
    • 0024544201 scopus 로고
    • Asymptomatic hyper-CK-emia: An electrophysiologic and histopathologic study
    • Joy JL, Oh SJ. Asymptomatic hyper-CK-emia: an electrophysiologic and histopathologic study. Muscle Nerve 1989 12 : 206 209.
    • (1989) Muscle Nerve , vol.12 , pp. 206-209
    • Joy, J.L.1    Oh, S.J.2
  • 15
    • 33244496467 scopus 로고    scopus 로고
    • Asymptomatic or minimally symptomatic hyperCKemia: Histopathologic correlates
    • Dabby R, Sadeh M, Herman O, et al. Asymptomatic or minimally symptomatic hyperCKemia: histopathologic correlates. Isr Med Assoc J 2006 8 : 110 113.
    • (2006) Isr Med Assoc J , vol.8 , pp. 110-113
    • Dabby, R.1    Sadeh, M.2    Herman, O.3
  • 16
    • 54749098890 scopus 로고    scopus 로고
    • Muscle biopsy and in vitro contracture test in subjects with idiopathic HyperCKemia
    • Malandrini A, Orrico A, Gaudiano C, et al. Muscle biopsy and in vitro contracture test in subjects with idiopathic HyperCKemia. Anesthesiology 2008 109 : 625 628.
    • (2008) Anesthesiology , vol.109 , pp. 625-628
    • Malandrini, A.1    Orrico, A.2    Gaudiano, C.3
  • 17
    • 17044449846 scopus 로고    scopus 로고
    • Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia
    • Carbone I, Bruno C, Sotgia F, et al. Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia. Neurology 2000 54 : 1373 1376.
    • (2000) Neurology , vol.54 , pp. 1373-1376
    • Carbone, I.1    Bruno, C.2    Sotgia, F.3
  • 18
    • 1342267006 scopus 로고    scopus 로고
    • Caveolinopathies: Mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases
    • Woodman SE, Sotgia F, Galbiati F, Minetti C, Lisanti MP. Caveolinopathies: mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases. Neurology 2004 62 : 538 543.
    • (2004) Neurology , vol.62 , pp. 538-543
    • Woodman, S.E.1    Sotgia, F.2    Galbiati, F.3    Minetti, C.4    Lisanti, M.P.5
  • 19
    • 0036299366 scopus 로고    scopus 로고
    • Familial isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) gene
    • Merlini L, Carbone I, Capanni C, et al. Familial isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) gene. J Neurol Neurosurg Psychiatry 2002 73 : 65 67.
    • (2002) J Neurol Neurosurg Psychiatry , vol.73 , pp. 65-67
    • Merlini, L.1    Carbone, I.2    Capanni, C.3
  • 20
    • 34347403691 scopus 로고    scopus 로고
    • Frequency of calpain-3 c.550delA mutation in limb girdle muscular dystrophy type 2 and isolated hyperCKemia in German patients
    • Hanisch F, Muller CR, Grimm D, et al. Frequency of calpain-3 c.550delA mutation in limb girdle muscular dystrophy type 2 and isolated hyperCKemia in German patients. Clin Neuropathol 2007 26 : 157 163.
    • (2007) Clin Neuropathol , vol.26 , pp. 157-163
    • Hanisch, F.1    Muller, C.R.2    Grimm, D.3
  • 21
    • 67449119353 scopus 로고    scopus 로고
    • Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
    • Fanin M, Nascimbeni AC, Aurino S, et al. Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes. Neurology 2009 72 : 1432 1435.
    • (2009) Neurology , vol.72 , pp. 1432-1435
    • Fanin, M.1    Nascimbeni, A.C.2    Aurino, S.3
  • 22
    • 0030247740 scopus 로고    scopus 로고
    • Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle
    • Prelle A, Rigoletto C, Moggio M, et al. Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle. J Neurol Sci 1996 140 : 132 136.
    • (1996) J Neurol Sci , vol.140 , pp. 132-136
    • Prelle, A.1    Rigoletto, C.2    Moggio, M.3
  • 23
    • 45449100121 scopus 로고    scopus 로고
    • Clinical, genetic, and cardiac magnetic resonance imaging findings in primary desminopathies
    • Strach K, Sommer T, Grohe C, et al. Clinical, genetic, and cardiac magnetic resonance imaging findings in primary desminopathies. Neuromuscul Disord 2008 18 : 475 482.
    • (2008) Neuromuscul Disord , vol.18 , pp. 475-482
    • Strach, K.1    Sommer, T.2    Grohe, C.3
  • 24
    • 34547882325 scopus 로고    scopus 로고
    • Phenotypic study in 40 patients with dysferlin gene mutations: High frequency of atypical phenotypes
    • Nguyen K, Bassez G, Krahn M, et al. Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes. Arch Neurol 2007 64 : 1176 1182.
    • (2007) Arch Neurol , vol.64 , pp. 1176-1182
    • Nguyen, K.1    Bassez, G.2    Krahn, M.3
  • 25
    • 28944454254 scopus 로고    scopus 로고
    • Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I
    • Boito CA, Melacini P, Vianello A, et al. Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I. Arch Neurol 2005 62 : 1894 1899.
    • (2005) Arch Neurol , vol.62 , pp. 1894-1899
    • Boito, C.A.1    Melacini, P.2    Vianello, A.3
  • 26
    • 60549088537 scopus 로고    scopus 로고
    • Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion
    • Ferreiro V, Giliberto F, Muniz GM, et al. Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion. Muscle Nerve 2009 39 : 239 243.
    • (2009) Muscle Nerve , vol.39 , pp. 239-243
    • Ferreiro, V.1    Giliberto, F.2    Muniz, G.M.3
  • 27
    • 33645716619 scopus 로고    scopus 로고
    • Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: Case series
    • Ramelli GP, Joncourt F, Luetschg J, Weis J, Tolnay M, Burgunder JM. Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series. Swiss Med Wkly 2006 136 : 189 193.
    • (2006) Swiss Med Wkly , vol.136 , pp. 189-193
    • Ramelli, G.P.1    Joncourt, F.2    Luetschg, J.3    Weis, J.4    Tolnay, M.5    Burgunder, J.M.6
  • 30
    • 0031811334 scopus 로고    scopus 로고
    • Homozygous alpha-sarcoglycan mutation in two siblings: One asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient
    • Angelini C, Fanin M, Menegazzo E, Freda MP, Duggan DJ, Hoffman EP. Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient. Muscle Nerve 1998 21 : 769 775.
    • (1998) Muscle Nerve , vol.21 , pp. 769-775
    • Angelini, C.1    Fanin, M.2    Menegazzo, E.3    Freda, M.P.4    Duggan, D.J.5    Hoffman, E.P.6
  • 31
    • 19544393908 scopus 로고    scopus 로고
    • Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2
    • Merlini L, Sabatelli P, Columbaro M, et al. Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2. Muscle Nerve 2005 31 : 764 767.
    • (2005) Muscle Nerve , vol.31 , pp. 764-767
    • Merlini, L.1    Sabatelli, P.2    Columbaro, M.3
  • 32
    • 33845696843 scopus 로고    scopus 로고
    • Follow-up of a large population of asymptomatic/oligosymptomatic hyperckemic subjects
    • D'Adda E, Sciacco M, Fruguglietti ME, et al. Follow-up of a large population of asymptomatic/oligosymptomatic hyperckemic subjects. J Neurol 2006 253 : 1399 1403.
    • (2006) J Neurol , vol.253 , pp. 1399-1403
    • D'Adda, E.1    Sciacco, M.2    Fruguglietti, M.E.3
  • 34
    • 0030909759 scopus 로고    scopus 로고
    • Malignant hyperthermia testing in patients with persistently increased serum creatine kinase levels
    • Weglinski MR, Wedel DJ, Engel AG. Malignant hyperthermia testing in patients with persistently increased serum creatine kinase levels. Anesth Analg 1997 84 : 1038 1041.
    • (1997) Anesth Analg , vol.84 , pp. 1038-1041
    • Weglinski, M.R.1    Wedel, D.J.2    Engel, A.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.