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Volumn 28, Issue 2, 2008, Pages 185-194

Charcot-Marie-Tooth neuropathies: Diagnosis and management

Author keywords

Charcot Marie Tooth disease; Diagnosis; Heterogeneity; Treatment

Indexed keywords

AMITRIPTYLINE; ANTICONVULSIVE AGENT; ASCORBIC ACID; CARBAMAZEPINE; DESIPRAMINE; GABAPENTIN; IMMUNOMODULATING AGENT; LAMOTRIGINE; LIDOCAINE; NORTRIPTYLINE; ONAPRISTONE; PREGABALIN; TRICYCLIC ANTIDEPRESSANT AGENT;

EID: 41149085223     PISSN: 02718235     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1062264     Document Type: Review
Times cited : (65)

References (54)
  • 1
    • 0016266593 scopus 로고
    • Genetic and clinical aspects of Charcot-Marie-Tooth's disease
    • Skre H. Genetic and clinical aspects of Charcot-Marie-Tooth's disease. Clin Genet 1974;6:98-118
    • (1974) Clin Genet , vol.6 , pp. 98-118
    • Skre, H.1
  • 2
    • 84882866259 scopus 로고    scopus 로고
    • The hereditary motor and sensory neuropathies: An overview of the clinical, genetic, electrophysiologic and pathologic features
    • Dyck PJ, ed, 4th ed. Philadelphia: WB Saunders;
    • Shy M, Lupski JR, Chance PF, Klein CJ, Dyck P. The hereditary motor and sensory neuropathies: an overview of the clinical, genetic, electrophysiologic and pathologic features. In: Dyck PJ, ed. Peripheral Neuropathy. 4th ed. Philadelphia: WB Saunders; 2005:1623-1658
    • (2005) Peripheral Neuropathy , pp. 1623-1658
    • Shy, M.1    Lupski, J.R.2    Chance, P.F.3    Klein, C.J.4    Dyck, P.5
  • 3
    • 33747209344 scopus 로고    scopus 로고
    • No mutation was detected in the LMNA gene among sporadic Charcot-Marie-Tooth patients
    • Song SJ, Zhang YZ, Chen B, et al. No mutation was detected in the LMNA gene among sporadic Charcot-Marie-Tooth patients. Beijing Da Xue Xue Bao 2006;38:78-79
    • (2006) Beijing Da Xue Xue Bao , vol.38 , pp. 78-79
    • Song, S.J.1    Zhang, Y.Z.2    Chen, B.3
  • 4
    • 0002896804 scopus 로고
    • Sue une forme particulaire d'atrophie musculaire progressive souvent familial debutant par les pieds et les jamber et atteingnant plus tard les mains.
    • Charcot J, Marie P. Sue une forme particulaire d'atrophie musculaire progressive souvent familial debutant par les pieds et les jamber et atteingnant plus tard les mains. Re Med 1886;6:97-138
    • (1886) Re Med , vol.6 , pp. 97-138
    • Charcot, J.1    Marie, P.2
  • 6
    • 0002649152 scopus 로고
    • Sur la nevritte interstitielle, hypertrophique et progressive de l'enfance.
    • Dejerine H, Sottas J. Sur la nevritte interstitielle, hypertrophique et progressive de l'enfance. CR Soc Biol Paris 1893;45:63-96
    • (1893) CR Soc Biol Paris , vol.45 , pp. 63-96
    • Dejerine, H.1    Sottas, J.2
  • 7
    • 0001210517 scopus 로고
    • A sept cas d'une maladie familiale particulaire.
    • Roussy G, Levy G. A sept cas d'une maladie familiale particulaire. Rev Neurol 1926;33:427-450
    • (1926) Rev Neurol , vol.33 , pp. 427-450
    • Roussy, G.1    Levy, G.2
  • 8
    • 0011900910 scopus 로고
    • Über die neurotische Muskelatrophie Charcot-Marie: Klinisch-genetische Studien.
    • Dawidenkow S. Über die neurotische Muskelatrophie Charcot-Marie: Klinisch-genetische Studien. Z Ges Neurol Psychiat 1927;107:259
    • (1927) Z Ges Neurol Psychiat , vol.107 , pp. 259
    • Dawidenkow, S.1
  • 9
    • 0011853208 scopus 로고
    • Über dir neurotische Muskelatrophie Charcot-Marie: Klinisch-genetische Studien.
    • Dawidenkow S. Über dir neurotische Muskelatrophie Charcot-Marie: Klinisch-genetische Studien. Z Neurol 1927; 108:344
    • (1927) Z Neurol , vol.108 , pp. 344
    • Dawidenkow, S.1
  • 10
    • 0014301112 scopus 로고
    • Lower motor and primary sensory neuron diseases with peroneal muscular atrophy: II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations
    • Dyck PJ, Lambert EH. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy: II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations. Arch Neurol 1968;18:619-625
    • (1968) Arch Neurol , vol.18 , pp. 619-625
    • Dyck, P.J.1    Lambert, E.H.2
  • 11
    • 0014301249 scopus 로고
    • Lower motor and primary sensory neuron diseases with peroneal muscular atrophy: I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies
    • Dyck PJ, Lambert EH. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy: I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. Arch Neurol 1968;18:603-618
    • (1968) Arch Neurol , vol.18 , pp. 603-618
    • Dyck, P.J.1    Lambert, E.H.2
  • 12
    • 0018942439 scopus 로고
    • The clinical features of hereditary motor and sensory neuropathy types I and II
    • Harding AE, Thomas PK. The clinical features of hereditary motor and sensory neuropathy types I and II. Brain 1980;103: 259-280
    • (1980) Brain , vol.103 , pp. 259-280
    • Harding, A.E.1    Thomas, P.K.2
  • 13
    • 0018949405 scopus 로고
    • Genetic aspects of hereditary motor and sensory neuropathy (types I and II)
    • Harding AE, Thomas PK. Genetic aspects of hereditary motor and sensory neuropathy (types I and II). J Med Genet 1980;17:329-336
    • (1980) J Med Genet , vol.17 , pp. 329-336
    • Harding, A.E.1    Thomas, P.K.2
  • 14
  • 15
    • 0017744163 scopus 로고
    • Myelination of mouse axons by Schwann cells transplanted from normal and abnormal human nerves
    • Aguayo AJ, Kasarjian J, Skamene E, Kongshavn P, Bray GM. Myelination of mouse axons by Schwann cells transplanted from normal and abnormal human nerves. Nature 1977;268:753-755
    • (1977) Nature , vol.268 , pp. 753-755
    • Aguayo, A.J.1    Kasarjian, J.2    Skamene, E.3    Kongshavn, P.4    Bray, G.M.5
  • 16
    • 0025868571 scopus 로고
    • DNA duplication associated with Charcot-Marie-Tooth disease type 1A
    • Lupski JR, de Oca-Luna RM, Slaugenhaupt S, et al. DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell 1991;66:219-232
    • (1991) Cell , vol.66 , pp. 219-232
    • Lupski, J.R.1    de Oca-Luna, R.M.2    Slaugenhaupt, S.3
  • 17
    • 0025997898 scopus 로고
    • Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). The HMSN Collaborative Research Group
    • Raeymaekers P, Timmerman V, Nelis E, et al. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). The HMSN Collaborative Research Group. Neuromuscul Disord 1991;1:93-97
    • (1991) Neuromuscul Disord , vol.1 , pp. 93-97
    • Raeymaekers, P.1    Timmerman, V.2    Nelis, E.3
  • 18
    • 10744221158 scopus 로고    scopus 로고
    • Phenotypic clustering in MPZ mutations
    • Shy ME, Jani A, Krajewski KM, et al. Phenotypic clustering in MPZ mutations. Brain 2004;127:371-384
    • (2004) Brain , vol.127 , pp. 371-384
    • Shy, M.E.1    Jani, A.2    Krajewski, K.M.3
  • 19
    • 0017374733 scopus 로고    scopus 로고
    • Bradley WG, Madrid R, Davis CJ. The peroneal muscular atrophy syndrome. Clinical, genetic, electrophysiological and nerve biopsy studies. Part 3: Clinical, electrophysiological and pathological correlations. J Neurol Sci 1977;32: 123-136
    • Bradley WG, Madrid R, Davis CJ. The peroneal muscular atrophy syndrome. Clinical, genetic, electrophysiological and nerve biopsy studies. Part 3: Clinical, electrophysiological and pathological correlations. J Neurol Sci 1977;32: 123-136
  • 20
    • 0025218902 scopus 로고
    • Hereditary induced peripheral neuropathies
    • Lovelace R. Hereditary induced peripheral neuropathies. Clin Podiatr Med Surg 1990;7:37-50
    • (1990) Clin Podiatr Med Surg , vol.7 , pp. 37-50
    • Lovelace, R.1
  • 21
    • 0027723256 scopus 로고
    • Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families
    • Nicholson G, Nash J. Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families. Neurology 1993;43:2558-2564
    • (1993) Neurology , vol.43 , pp. 2558-2564
    • Nicholson, G.1    Nash, J.2
  • 22
    • 0029863589 scopus 로고    scopus 로고
    • Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: A European collaborative study
    • Nelis E, Van Broeckhoven C, De Jonghe P, et al. Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study. Eur J Hum Genet 1996;4:25-33
    • (1996) Eur J Hum Genet , vol.4 , pp. 25-33
    • Nelis, E.1    Van Broeckhoven, C.2    De Jonghe, P.3
  • 23
    • 32044474017 scopus 로고    scopus 로고
    • T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy
    • Shy ME, Scavina MT, Clark A, et al. T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy. Ann Neurol 2006;59:358-364
    • (2006) Ann Neurol , vol.59 , pp. 358-364
    • Shy, M.E.1    Scavina, M.T.2    Clark, A.3
  • 24
    • 0019494495 scopus 로고
    • Intensive evaluation of unclassified neuropathies yields improved diagnosis
    • Dyck PJ, Oviatt KF, Lambert EH. Intensive evaluation of unclassified neuropathies yields improved diagnosis. Ann Neurol 1981;10:222-226
    • (1981) Ann Neurol , vol.10 , pp. 222-226
    • Dyck, P.J.1    Oviatt, K.F.2    Lambert, E.H.3
  • 25
    • 0023708417 scopus 로고
    • X-linked dominant Charcot-Marie-Tooth neuropathy with 15 cases in a family genetic linkage study
    • Ionasescu W, Burns TL, Searby C, Ionasescu R. X-linked dominant Charcot-Marie-Tooth neuropathy with 15 cases in a family genetic linkage study. Muscle Nerve 1988;11:1154-1156
    • (1988) Muscle Nerve , vol.11 , pp. 1154-1156
    • Ionasescu, W.1    Burns, T.L.2    Searby, C.3    Ionasescu, R.4
  • 26
    • 0027374931 scopus 로고
    • Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication
    • Wise CA, Garcia CA, Davis SN, et al. Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication. Am J Hum Genet 1993;53:853-863
    • (1993) Am J Hum Genet , vol.53 , pp. 853-863
    • Wise, C.A.1    Garcia, C.A.2    Davis, S.N.3
  • 27
    • 0842304504 scopus 로고    scopus 로고
    • Loss-of-function phenotype of hereditary neuropathy with liability to pressure palsies
    • Li J, Krajewski K, Lewis RA, Shy ME. Loss-of-function phenotype of hereditary neuropathy with liability to pressure palsies. Muscle Nerve 2004;29:205-210
    • (2004) Muscle Nerve , vol.29 , pp. 205-210
    • Li, J.1    Krajewski, K.2    Lewis, R.A.3    Shy, M.E.4
  • 28
    • 0033554348 scopus 로고    scopus 로고
    • Mutation testing in Charcot-Marie-Tooth neuropathy
    • Nicholson GA. Mutation testing in Charcot-Marie-Tooth neuropathy. Ann N Y Acad Sci 1999;883:383-388
    • (1999) Ann N Y Acad Sci , vol.883 , pp. 383-388
    • Nicholson, G.A.1
  • 29
    • 0027359513 scopus 로고
    • Screening of dominantly inherited Charcot-Marie-Tooth neuropathies
    • Ionasescu W, Ionasescu R, Searby C. Screening of dominantly inherited Charcot-Marie-Tooth neuropathies. Muscle Nerve 1993;16:1232-1238
    • (1993) Muscle Nerve , vol.16 , pp. 1232-1238
    • Ionasescu, W.1    Ionasescu, R.2    Searby, C.3
  • 30
    • 33745273262 scopus 로고    scopus 로고
    • Therapeutic strategies for the inherited neuropathies
    • Shy ME. Therapeutic strategies for the inherited neuropathies. Neuromolecular Med 2006;8:255-278
    • (2006) Neuromolecular Med , vol.8 , pp. 255-278
    • Shy, M.E.1
  • 31
    • 0141833983 scopus 로고    scopus 로고
    • Disease mechanisms in inherited neuropathies
    • Suter U, Scherer SS. Disease mechanisms in inherited neuropathies. Nat Rev Neurosci 2003;4:714-726
    • (2003) Nat Rev Neurosci , vol.4 , pp. 714-726
    • Suter, U.1    Scherer, S.S.2
  • 32
    • 0034065232 scopus 로고    scopus 로고
    • On the molecular architecture of myelinated fibers
    • Arroyo EJ, Scherer SS. On the molecular architecture of myelinated fibers. Histochem Cell Biol 2000;113:1-18
    • (2000) Histochem Cell Biol , vol.113 , pp. 1-18
    • Arroyo, E.J.1    Scherer, S.S.2
  • 34
    • 0033963592 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth disease type 1: Molecular pathogenesis to gene therapy
    • Kamholz J, Menichella D, Jani A, et al. Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapy. Brain 2000;123:222-233
    • (2000) Brain , vol.123 , pp. 222-233
    • Kamholz, J.1    Menichella, D.2    Jani, A.3
  • 35
    • 84903029662 scopus 로고    scopus 로고
    • Inherited neuropathies: Clinical, genetic, and biological features
    • Lazzarini RA, ed, London: Elsevier;
    • Wrabetz L, Feltri ML, Kleopa K. Inherited neuropathies: clinical, genetic, and biological features. In: Lazzarini RA, ed. Myelin Biology and Disorders. London: Elsevier; 2004: 905-952
    • (2004) Myelin Biology and Disorders , pp. 905-952
    • Wrabetz, L.1    Feltri, M.L.2    Kleopa, K.3
  • 36
    • 2342444048 scopus 로고    scopus 로고
    • Axonal neuregulin-1 regulates myelin sheath thickness
    • Michailov GV, Sereda MW, Brinkmann BG, et al. Axonal neuregulin-1 regulates myelin sheath thickness. Science 2004;304:700-703
    • (2004) Science , vol.304 , pp. 700-703
    • Michailov, G.V.1    Sereda, M.W.2    Brinkmann, B.G.3
  • 37
    • 23944503110 scopus 로고    scopus 로고
    • Neuregulin-1 type III determines the ensheathment fate of axons
    • Taveggia C, Zanazzi G, Petrylak A, et al. Neuregulin-1 type III determines the ensheathment fate of axons. Neuron 2005-47:681-694
    • (2005) Neuron , pp. 681-694
    • Taveggia, C.1    Zanazzi, G.2    Petrylak, A.3
  • 38
    • 0033809078 scopus 로고    scopus 로고
    • Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis
    • Lewis RA, Sumner AJ, Shy ME. Electrophysiological features of inherited demyelinating neuropathies: a reappraisal in the era of molecular diagnosis. Muscle Nerve 2000; 23:1472-1487
    • (2000) Muscle Nerve , vol.23 , pp. 1472-1487
    • Lewis, R.A.1    Sumner, A.J.2    Shy, M.E.3
  • 39
    • 0017872262 scopus 로고
    • Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome
    • Brust JC, Lovelace RE, Devi S. Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome. Acta Neurol Scand Suppl 1978;68:1-142
    • (1978) Acta Neurol Scand Suppl , vol.68 , pp. 1-142
    • Brust, J.C.1    Lovelace, R.E.2    Devi, S.3
  • 40
    • 0018222952 scopus 로고
    • The peroneal muscular atrophy syndrome: Clinical, genetic, electrophysiological and nerve biopsy findings and classification
    • Davis CJF, Bradley WG, Madrid R. The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy findings and classification. J Genet Hum 1978; 26:311-349
    • (1978) J Genet Hum , vol.26 , pp. 311-349
    • Davis, C.J.F.1    Bradley, W.G.2    Madrid, R.3
  • 41
    • 0033921060 scopus 로고    scopus 로고
    • Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A
    • Krajewski KM, Lewis RA, Fuerst DR, et al. Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A. Brain 2000;123:1516-1527
    • (2000) Brain , vol.123 , pp. 1516-1527
    • Krajewski, K.M.1    Lewis, R.A.2    Fuerst, D.R.3
  • 42
    • 25444531406 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth disease impairs quality of life: Why? And how do we improve it?
    • Shy ME, Rose MR. Charcot-Marie-Tooth disease impairs quality of life: why? And how do we improve it? Neurology 2005;65:790-791
    • (2005) Neurology , vol.65 , pp. 790-791
    • Shy, M.E.1    Rose, M.R.2
  • 43
    • 33646789831 scopus 로고    scopus 로고
    • Vulvodynia: Characteristics and associations with comorbidities and quality of life
    • Arnold LD, Bachmann GA, Rosen R, Kelly S, Rhoads GG. Vulvodynia: characteristics and associations with comorbidities and quality of life. Obstet Gynecol 2006;107:617-624
    • (2006) Obstet Gynecol , vol.107 , pp. 617-624
    • Arnold, L.D.1    Bachmann, G.A.2    Rosen, R.3    Kelly, S.4    Rhoads, G.G.5
  • 44
    • 25444449876 scopus 로고    scopus 로고
    • Quality of life in patients with Charcot-Marie-Tooth disease
    • Vinci P, Serrao M, Millul A, et al. Quality of life in patients with Charcot-Marie-Tooth disease. Neurology 2005;65:922-924
    • (2005) Neurology , vol.65 , pp. 922-924
    • Vinci, P.1    Serrao, M.2    Millul, A.3
  • 45
    • 33846387467 scopus 로고    scopus 로고
    • The importance of assessing quality of life in patients with neuromuscular disorders
    • Carter GT, Han JJ, Abresch RT, Jensen MP. The importance of assessing quality of life in patients with neuromuscular disorders. Am J Hosp Palliat Care 2006;23: 493-497
    • (2006) Am J Hosp Palliat Care , vol.23 , pp. 493-497
    • Carter, G.T.1    Han, J.J.2    Abresch, R.T.3    Jensen, M.P.4
  • 46
    • 2942705992 scopus 로고    scopus 로고
    • Genetic testing in neuromuscular disease
    • Krajewski KM, Shy ME. Genetic testing in neuromuscular disease. Neurol Clin 2004;22:481-508
    • (2004) Neurol Clin , vol.22 , pp. 481-508
    • Krajewski, K.M.1    Shy, M.E.2
  • 47
    • 0032710350 scopus 로고    scopus 로고
    • Risks and benefits of DNA testing for neurogenetic disorders
    • Bird TD. Risks and benefits of DNA testing for neurogenetic disorders. Semin Neurol 1999;19:253-259
    • (1999) Semin Neurol , vol.19 , pp. 253-259
    • Bird, T.D.1
  • 48
    • 0036157054 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth disease and related neuropathies: Mutation distribution and genotype-phenotype correlation
    • Boerkoel CF, Takashima H, Garcia CA, et al. Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype correlation. Ann Neurol 2002;51:190-201
    • (2002) Ann Neurol , vol.51 , pp. 190-201
    • Boerkoel, C.F.1    Takashima, H.2    Garcia, C.A.3
  • 49
    • 15844393894 scopus 로고    scopus 로고
    • A transgenic rat model of Charcot-Marie-Tooth disease
    • Sereda M, Griffiths I, Puhlhofer A, et al. A transgenic rat model of Charcot-Marie-Tooth disease. Neuron 1996;16: 1049-1060
    • (1996) Neuron , vol.16 , pp. 1049-1060
    • Sereda, M.1    Griffiths, I.2    Puhlhofer, A.3
  • 50
    • 0344267738 scopus 로고    scopus 로고
    • Effective gene transfer of lacZ and P0 into Schwann cells of P0-deficient mice
    • Guenard V, Schweitzer B, Flechsig E, et al. Effective gene transfer of lacZ and P0 into Schwann cells of P0-deficient mice. Glia 1999;25:165-178
    • (1999) Glia , vol.25 , pp. 165-178
    • Guenard, V.1    Schweitzer, B.2    Flechsig, E.3
  • 51
    • 41149095244 scopus 로고    scopus 로고
    • AAV-GDNF improves neuropathy in MPZ-/- mice
    • lanokova E, Lewis R, Acsadi G, et al. AAV-GDNF improves neuropathy in MPZ-/- mice. Neurology 2006;66 (suppl 2):A276
    • (2006) Neurology , vol.66 , Issue.SUPPL. 2
    • lanokova, E.1    Lewis, R.2    Acsadi, G.3
  • 52
    • 0036252837 scopus 로고    scopus 로고
    • Role of immune cells in animal models for inherited neuropathies: Facts and visions
    • Maurer M, Kobsar I, Berghoff M, Schmid CD, Carenini S, Martini R. Role of immune cells in animal models for inherited neuropathies: facts and visions. J Anat 2002;200: 405-414
    • (2002) J Anat , vol.200 , pp. 405-414
    • Maurer, M.1    Kobsar, I.2    Berghoff, M.3    Schmid, C.D.4    Carenini, S.5    Martini, R.6
  • 53
    • 1942422646 scopus 로고    scopus 로고
    • Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease
    • Passage E, Norreel JC, Noack-Fraissignes P, et al. Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease. Nat Med 2004;10:396-401
    • (2004) Nat Med , vol.10 , pp. 396-401
    • Passage, E.1    Norreel, J.C.2    Noack-Fraissignes, P.3
  • 54
    • 0347185347 scopus 로고    scopus 로고
    • Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A)
    • Sereda MW, Meyer Zu Horste G, Suter U, Uzma N, Nave KA. Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A). Nat Med 2003;9:1533-1537
    • (2003) Nat Med , vol.9 , pp. 1533-1537
    • Sereda, M.W.1    Meyer, Z.2    Horste, G.3    Suter, U.4    Uzma, N.5    Nave, K.A.6


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