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Volumn 62, Issue 2, 2007, Pages 107-109

Myelin mishaps

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN; PROTEOLIPID PROTEIN;

EID: 35148825118     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.21165     Document Type: Editorial
Times cited : (4)

References (11)
  • 1
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    • Phenotypic characterization of hypomyelination and congenital cataracts
    • Biancheri R, Zara F, Bruno C, et al. Phenotypic characterization of hypomyelination and congenital cataracts. Ann Neurol 2007:62;121-127.
    • (2007) Ann Neurol , vol.62 , pp. 121-127
    • Biancheri, R.1    Zara, F.2    Bruno, C.3
  • 2
    • 0026410630 scopus 로고
    • Pattern recognition in magnetic resonance imaging of white matter disorders in children and young adults
    • van der Knaap MS, Valk J, de Neeling N, Nauta JJ. Pattern recognition in magnetic resonance imaging of white matter disorders in children and young adults. Neuroradiology 1991;33: 478-493.
    • (1991) Neuroradiology , vol.33 , pp. 478-493
    • van der Knaap, M.S.1    Valk, J.2    de Neeling, N.3    Nauta, J.J.4
  • 3
    • 0030975392 scopus 로고    scopus 로고
    • A new leukoencephalopathy with vanishing white matter
    • van der Knaap MS, Barth PG, Gabreëls FJM, et al. A new leukoencephalopathy with vanishing white matter. Neurology 1997;48:845-855.
    • (1997) Neurology , vol.48 , pp. 845-855
    • van der Knaap, M.S.1    Barth, P.G.2    Gabreëls, F.J.M.3
  • 4
    • 0032886533 scopus 로고    scopus 로고
    • Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach
    • van der Knaap M, Breiter S, Naidu S, et al. Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach. Radiology 1999;213:121-133.
    • (1999) Radiology , vol.213 , pp. 121-133
    • van der Knaap, M.1    Breiter, S.2    Naidu, S.3
  • 5
    • 0036793880 scopus 로고    scopus 로고
    • New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellum
    • van der Knaap M, Naidu S, Pouwels P, et al. New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellum. AJNR Am J Neuroradiol 2002;23:1466-1474.
    • (2002) AJNR Am J Neuroradiol , vol.23 , pp. 1466-1474
    • van der Knaap, M.1    Naidu, S.2    Pouwels, P.3
  • 6
    • 0029973244 scopus 로고    scopus 로고
    • Histopathology of an infantile-onset spongiform leukoencephalopathy with a discrepantly mild clinical course
    • van der Knaap M, Barth P, Vrensen G, Valk J. Histopathology of an infantile-onset spongiform leukoencephalopathy with a discrepantly mild clinical course. Acta Neuropathol (Berl) 1996; 92:206-212.
    • (1996) Acta Neuropathol (Berl) , vol.92 , pp. 206-212
    • van der Knaap, M.1    Barth, P.2    Vrensen, G.3    Valk, J.4
  • 7
    • 35148840706 scopus 로고    scopus 로고
    • 2 Gangliosidosis. In: van der Knaap MS, Valk J. Magnetic resonance of myelination and myelin disorders. 3rd ed. Berlin: Springer, 2005: 103-111.
    • 2 Gangliosidosis. In: van der Knaap MS, Valk J. Magnetic resonance of myelination and myelin disorders. 3rd ed. Berlin: Springer, 2005: 103-111.
  • 8
    • 0026348463 scopus 로고
    • Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease
    • Raskind WH, Williams CA, Hudson LD, Bird TD. Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease. Am J Hum Genet 1991; 49:1355-1360.
    • (1991) Am J Hum Genet , vol.49 , pp. 1355-1360
    • Raskind, W.H.1    Williams, C.A.2    Hudson, L.D.3    Bird, T.D.4
  • 9
    • 0030020210 scopus 로고    scopus 로고
    • A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch family
    • Sistermans EA, de Wijs IJ, de Coo RF, et al. A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch family. Hum Genet 1996;97:337-339.
    • (1996) Hum Genet , vol.97 , pp. 337-339
    • Sistermans, E.A.1    de Wijs, I.J.2    de Coo, R.F.3
  • 10
    • 0031801082 scopus 로고    scopus 로고
    • Duplication of the proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease
    • Sistermans EA, de Coo rFM, De Wijs IJ, Van Oost BA. Duplication of the proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease. Neurology 1998;50:1749-1754.
    • (1998) Neurology , vol.50 , pp. 1749-1754
    • Sistermans, E.A.1    de Coo rFM, D.2    Wijs, I.J.3    Van Oost, B.A.4
  • 11
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    • Childhood white matter disorders: Quantitative MR imaging and spectroscopy
    • van der Voorn JP, Pouwels PJW, Hart AAM, et al. Childhood white matter disorders: quantitative MR imaging and spectroscopy. Radiology 2006;241:510-517.
    • (2006) Radiology , vol.241 , pp. 510-517
    • van der Voorn, J.P.1    Pouwels, P.J.W.2    Hart, A.A.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.