Magnetic resonance techniques in the assessment of myelin and myelination

被引:99
作者
Barkovich, AJ [1 ]
机构
[1] Univ Calif San Francisco, San Francisco, CA 94143 USA
关键词
D O I
10.1007/s10545-005-5952-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Leukodystrophy is a common central nervous system manifestation of inborn errors of metabolism. Until magnetic resonance imaging (MRI) emerged as a clinical tool, the diagnosis of leukodystrophy was difficult and imprecise; MRI has allowed new understandings and classifications of leukodystrophies that have greatly enhanced both our diagnostic ability and our understanding of these complex disorders. However, optimal use of MRI in this setting requires a fundamental understanding of myelin structure, myelin development, and the changes seen on MRI with myelination and demyelination. The purpose of this review is to provide the reader with the necessary tools for the use of MRI to diagnose and follow patients with leukodystrophies.
引用
收藏
页码:311 / 343
页数:33
相关论文
共 113 条
  • [81] QUARLES RH, 1985, RES METHODS NEUROCHE, V6, P303
  • [82] RASKIND WH, 1991, AM J HUM GENET, V49, P1355
  • [83] ADULT AND NEONATAL HUMAN BRAIN - DIFFUSIONAL ANISOTROPY AND MYELINATION WITH DIFFUSION-WEIGHTED MR IMAGING
    SAKUMA, H
    NOMURA, Y
    TAKEDA, K
    TAGAMI, T
    NAKAGAWA, T
    TAMAGAWA, Y
    ISHII, Y
    TSUKAMOTO, T
    [J]. RADIOLOGY, 1991, 180 (01) : 229 - 233
  • [84] X-linked creatine-transporter gene (SLC6A8) defect:: A new creatine-deficiency syndrome
    Salomons, GS
    van Dooren, SJM
    Verhoeven, NM
    Cecil, KM
    Ball, WS
    Degrauw, TJ
    Jakobs, C
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (06) : 1497 - 1500
  • [85] 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
    deWijs, IJ
    deCoo, RFM
    Smit, LME
    Menko, FH
    vanOost, BA
    [J]. HUMAN GENETICS, 1996, 97 (03) : 337 - 339
  • [86] 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
    [J]. NEUROLOGY, 1998, 50 (06) : 1749 - 1754
  • [87] MYELINATION OF THE BRAIN IN MRI - A STAGING SYSTEM
    STAUDT, M
    SCHROPP, C
    STAUDT, F
    OBLETTER, N
    BISE, K
    BREIT, A
    [J]. PEDIATRIC RADIOLOGY, 1993, 23 (03) : 169 - 176
  • [88] MRI ASSESSMENT OF MYELINATION - AN AGE STANDARDIZATION
    STAUDT, M
    SCHROPP, C
    STAUDT, F
    OBLETTER, N
    BISE, K
    BREIT, A
    WEINMANN, HM
    [J]. PEDIATRIC RADIOLOGY, 1994, 24 (02) : 122 - 127
  • [89] Stecca B, 2000, J NEUROSCI, V20, P4002