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Volumn 87, Issue , 2016, Pages 50-58

Hypomyelinating disorders: An MRI approach

Author keywords

Dysmyelinating and demyelinating disorders; Genetic leukoencephalopathies; Hypomyelinating disorders

Indexed keywords

CLINICAL FEATURE; DEMYELINATING DISEASE; DIFFUSION WEIGHTED IMAGING; DISEASE CLASSIFICATION; DISEASE COURSE; GENETIC DISORDER; HUMAN; HYPOMYELINATING DISORDER; IMAGING SYSTEM; INBORN ERROR OF METABOLISM; LEUKODYSTROPHY; LEUKOENCEPHALOPATHY; MYELIN WATER FRACTION IMAGING; MYELINATION; NEUROLOGIC DISEASE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REVIEW; SYSTEMIC DISEASE; WHITE MATTER; ANIMAL; BRAIN; METABOLISM; MYELIN SHEATH; PATHOLOGY; PROCEDURES;

EID: 84951083885     PISSN: 09699961     EISSN: 1095953X     Source Type: Journal    
DOI: 10.1016/j.nbd.2015.10.015     Document Type: Review
Times cited : (27)

References (111)
  • 1
    • 85011325143 scopus 로고    scopus 로고
    • Fundamentals of MR spectroscopy
    • Cambridge, New York, J.H. Gillard, A.D. Waldman, P.B. Barker (Eds.)
    • Barker P.B. Fundamentals of MR spectroscopy. Clinical MR Imaging 2010, 5-20. Cambridge, New York. 2nd ed. J.H. Gillard, A.D. Waldman, P.B. Barker (Eds.).
    • (2010) Clinical MR Imaging , pp. 5-20
    • Barker, P.B.1
  • 2
    • 0034040115 scopus 로고    scopus 로고
    • Concepts of myelin and myelination in neuroradiology
    • Barkovich A.J. Concepts of myelin and myelination in neuroradiology. AJNR Am. J. Neuroradiol. 2000, 21(6):1099-1109.
    • (2000) AJNR Am. J. Neuroradiol. , vol.21 , Issue.6 , pp. 1099-1109
    • Barkovich, A.J.1
  • 3
    • 0023848868 scopus 로고
    • Normal maturation of the neonatal and infant brain: MR imaging at 1.5T
    • Barkovich A.J., Kjos B.O., Jackson D.E., Norman D. Normal maturation of the neonatal and infant brain: MR imaging at 1.5T. Radiology 1988, 166:173-180.
    • (1988) Radiology , vol.166 , pp. 173-180
    • Barkovich, A.J.1    Kjos, B.O.2    Jackson, D.E.3    Norman, D.4
  • 4
    • 42249100179 scopus 로고    scopus 로고
    • N-acetylaspartate and N-acetylaspartylglutamate. Neurobiology and clinical significance
    • Benarroch E.E. N-acetylaspartate and N-acetylaspartylglutamate. Neurobiology and clinical significance. Neurology 2008, 70:1353-1357.
    • (2008) Neurology , vol.70 , pp. 1353-1357
    • Benarroch, E.E.1
  • 5
    • 85045011215 scopus 로고    scopus 로고
    • Pol III-related leukodystrophies
    • Bernard G., Vanderver A. Pol III-related leukodystrophies. Gene Rev. 2012, (http://www.ncbi.nlm.nih.gov/pubmed/22855961).
    • (2012) Gene Rev.
    • Bernard, G.1    Vanderver, A.2
  • 6
    • 35148883885 scopus 로고    scopus 로고
    • Phenotypic characterization of hypomyelination and congenital cataract
    • Biancheri R., Zara F., Bruno C., et al. Phenotypic characterization of hypomyelination and congenital cataract. Ann. Neurol. 2007, 62:121-127.
    • (2007) Ann. Neurol. , vol.62 , pp. 121-127
    • Biancheri, R.1    Zara, F.2    Bruno, C.3
  • 7
    • 80052702127 scopus 로고    scopus 로고
    • Hypomyelination and congenital cataract: broadening the clinical phenotype
    • Biancheri R., Zara F., Rossi A., et al. Hypomyelination and congenital cataract: broadening the clinical phenotype. Arch. Neurol. 2011, 68(9):1191-1194.
    • (2011) Arch. Neurol. , vol.68 , Issue.9 , pp. 1191-1194
    • Biancheri, R.1    Zara, F.2    Rossi, A.3
  • 8
    • 84871204629 scopus 로고    scopus 로고
    • Expanded spectrum of Pelizaeus-Merzbacher-like disease: literature revision and description of a novel GJC2 mutation in an unusually severe form
    • Biancheri R., Rosano C., Denegri L., et al. Expanded spectrum of Pelizaeus-Merzbacher-like disease: literature revision and description of a novel GJC2 mutation in an unusually severe form. Eur. J. Hum. Genet. 2013, 21:34-39.
    • (2013) Eur. J. Hum. Genet. , vol.21 , pp. 34-39
    • Biancheri, R.1    Rosano, C.2    Denegri, L.3
  • 9
    • 27644564737 scopus 로고    scopus 로고
    • Characterization of the NMR behaviour of white matter in bovine brain
    • Bjarnson T.A., Vavasour I.M., Chia C.L.L., MacKay A.L. Characterization of the NMR behaviour of white matter in bovine brain. Magn. Reson. Med. 2005, 54:1072-1081.
    • (2005) Magn. Reson. Med. , vol.54 , pp. 1072-1081
    • Bjarnson, T.A.1    Vavasour, I.M.2    Chia, C.L.L.3    MacKay, A.L.4
  • 10
    • 33947522227 scopus 로고    scopus 로고
    • T Hart BA. Quantitative MRI-pathology correlations of brain white matter lesions developing in a non-human primate model of multiple sclerosis
    • Blezer E.L.A., Bauer J., Brok H.P.M., Nicolay K. t Hart BA. Quantitative MRI-pathology correlations of brain white matter lesions developing in a non-human primate model of multiple sclerosis. NMR Biomed. 2007, 20(2):90-103.
    • (2007) NMR Biomed. , vol.20 , Issue.2 , pp. 90-103
    • Blezer, E.L.A.1    Bauer, J.2    Brok, H.P.M.3    Nicolay, K.4
  • 11
    • 84876848499 scopus 로고    scopus 로고
    • Chapter 162 - inborn errors of brain myelin formation
    • Elsevier, M.L. Olivier Dulac, B.S. Harvey (Eds.)
    • Boespflug-tanguy O. Chapter 162 - inborn errors of brain myelin formation. Handbook of Clinical Neurology 2013, vol. 113:1581-1592. Elsevier. M.L. Olivier Dulac, B.S. Harvey (Eds.).
    • (2013) Handbook of Clinical Neurology , vol.113 , pp. 1581-1592
    • Boespflug-tanguy, O.1
  • 12
    • 84874771923 scopus 로고    scopus 로고
    • Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism
    • (March 1, 2013)
    • Daoud H., Tétreault M., Gibson W., et al. Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism. J. Med. Genet. 2013, 50(3):194-197. (March 1, 2013).
    • (2013) J. Med. Genet. , vol.50 , Issue.3 , pp. 194-197
    • Daoud, H.1    Tétreault, M.2    Gibson, W.3
  • 13
    • 84885344514 scopus 로고    scopus 로고
    • Neurological manifestations of oculodentodigital dysplasia: a Cx43 channelopathy of the central nervous system?
    • De Bock M., Kerrebrouck M., Wang N., Leybaert L. Neurological manifestations of oculodentodigital dysplasia: a Cx43 channelopathy of the central nervous system?. Front. Pharmacol. 2013, 4.
    • (2013) Front. Pharmacol. , vol.4
    • De Bock, M.1    Kerrebrouck, M.2    Wang, N.3    Leybaert, L.4
  • 14
    • 84919865242 scopus 로고    scopus 로고
    • Investigating the stability of mcDESPOT myelin water fraction values derived using a stochastic region contraction approach
    • Deoni S.C.L., Kolind S.H. Investigating the stability of mcDESPOT myelin water fraction values derived using a stochastic region contraction approach. Magn. Reson. Med. 2015, 73(1):161-169.
    • (2015) Magn. Reson. Med. , vol.73 , Issue.1 , pp. 161-169
    • Deoni, S.C.L.1    Kolind, S.H.2
  • 15
    • 80054770781 scopus 로고    scopus 로고
    • Misalignment of PLP/DM20 transmembrane domains determines protein misfolding in Pelizaeus-Merzbacher disease
    • Dhaunchak A.S., Colman D.R., Nave K.-A. Misalignment of PLP/DM20 transmembrane domains determines protein misfolding in Pelizaeus-Merzbacher disease. J. Neurosci 2011, 31(42):14961-14971.
    • (2011) J. Neurosci , vol.31 , Issue.42 , pp. 14961-14971
    • Dhaunchak, A.S.1    Colman, D.R.2    Nave, K.-A.3
  • 16
    • 18344412917 scopus 로고
    • MR evaluation of early myelination patterns in normal and developmentally delayed infants
    • Dietrich R.B., Bradley W.G., Zagaroza E.J., et al. MR evaluation of early myelination patterns in normal and developmentally delayed infants. AJNR Am. J. Neuroradiol. 1988, 9:69-76.
    • (1988) AJNR Am. J. Neuroradiol. , vol.9 , pp. 69-76
    • Dietrich, R.B.1    Bradley, W.G.2    Zagaroza, E.J.3
  • 17
  • 18
    • 33646473693 scopus 로고    scopus 로고
    • Assessment of the early organization and maturation of infants' cerebral white matter fiber bundles: a feasibility study using quantitative diffusion tensor imaging and tractography
    • Dubois J., Hertz-Pannier L., Dehaene-Lambertz G., Cointepas Y., Le Bihan D. Assessment of the early organization and maturation of infants' cerebral white matter fiber bundles: a feasibility study using quantitative diffusion tensor imaging and tractography. NeuroImage 2006, 30:1121-1132.
    • (2006) NeuroImage , vol.30 , pp. 1121-1132
    • Dubois, J.1    Hertz-Pannier, L.2    Dehaene-Lambertz, G.3    Cointepas, Y.4    Le Bihan, D.5
  • 19
    • 84906794628 scopus 로고    scopus 로고
    • The early development of brain white matter: a review of imaging studies in fetuses, newborns and infants
    • Dubois J., Dehaene-Lambertz G., Kulikova S., Poupon C., Hüppi P.S., Hertz-Pannier L. The early development of brain white matter: a review of imaging studies in fetuses, newborns and infants. Neuroscience 2014, 276:48-71.
    • (2014) Neuroscience , vol.276 , pp. 48-71
    • Dubois, J.1    Dehaene-Lambertz, G.2    Kulikova, S.3    Poupon, C.4    Hüppi, P.S.5    Hertz-Pannier, L.6
  • 20
    • 77950618784 scopus 로고    scopus 로고
    • Multiexponential T2, magnetization transfer, and quantitative histology in white matter tracts of rat spinal cord
    • Dula A.N., Gochberg D.F., Valentine H.L., Valentine W.M., Does M.D. Multiexponential T2, magnetization transfer, and quantitative histology in white matter tracts of rat spinal cord. Magn. Reson. Med. 2010, 63(4):902-909.
    • (2010) Magn. Reson. Med. , vol.63 , Issue.4 , pp. 902-909
    • Dula, A.N.1    Gochberg, D.F.2    Valentine, H.L.3    Valentine, W.M.4    Does, M.D.5
  • 21
    • 84951150643 scopus 로고    scopus 로고
    • Quantification and analysis in MR spectroscopy
    • Cambridge, New York, J.H. Gillard, A.D. Waldman, P.B. Barker (Eds.)
    • Ernst T. Quantification and analysis in MR spectroscopy. Clinical MR Imaging 2010, 21-29. Cambridge, New York. 2nd ed. J.H. Gillard, A.D. Waldman, P.B. Barker (Eds.).
    • (2010) Clinical MR Imaging , pp. 21-29
    • Ernst, T.1
  • 23
    • 54049139573 scopus 로고    scopus 로고
    • Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations
    • (October 1, 2008)
    • Faghri S., Tamura D., Kraemer K.H., DiGiovanna J.J. Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations. J. Med. Genet. 2008, 45(10):609-621. (October 1, 2008).
    • (2008) J. Med. Genet. , vol.45 , Issue.10 , pp. 609-621
    • Faghri, S.1    Tamura, D.2    Kraemer, K.H.3    DiGiovanna, J.J.4
  • 25
    • 84880014019 scopus 로고    scopus 로고
    • Microtubule-based transport - basic mechanisms, traffic rules and role in neurological pathogenesis
    • (June 1, 2013)
    • Franker M.A.M., Hoogenraad C.C. Microtubule-based transport - basic mechanisms, traffic rules and role in neurological pathogenesis. J. Cell Sci. 2013, 126(11):2319-2329. (June 1, 2013).
    • (2013) J. Cell Sci. , vol.126 , Issue.11 , pp. 2319-2329
    • Franker, M.A.M.1    Hoogenraad, C.C.2
  • 26
    • 0033554340 scopus 로고    scopus 로고
    • Peripheral neuropathy caused by proteolipid protein gene mutations
    • Garbern J.Y., Cambi F., Lewis R., et al. Peripheral neuropathy caused by proteolipid protein gene mutations. Ann. N. Y. Acad. Sci. 1999, 883(1):351-365.
    • (1999) Ann. N. Y. Acad. Sci. , vol.883 , Issue.1 , pp. 351-365
    • Garbern, J.Y.1    Cambi, F.2    Lewis, R.3
  • 27
    • 0034038644 scopus 로고    scopus 로고
    • Magnetization transfer and multicomponent T2 relaxation measurements with histopathologic correlation in an experimental model of MS
    • Gareau P.J., Rutt B.K., Karlik S.J., Mitchell J.R. Magnetization transfer and multicomponent T2 relaxation measurements with histopathologic correlation in an experimental model of MS. J. Magn. Reson. Imaging 2000, 11(6):586-595.
    • (2000) J. Magn. Reson. Imaging , vol.11 , Issue.6 , pp. 586-595
    • Gareau, P.J.1    Rutt, B.K.2    Karlik, S.J.3    Mitchell, J.R.4
  • 28
    • 3042781670 scopus 로고    scopus 로고
    • A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A
    • (07//print)
    • Giglia-Mari G., Coin F., Ranish J.A., et al. A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A. Nat. Genet. 2004, 36(7):714-719. (07//print).
    • (2004) Nat. Genet. , vol.36 , Issue.7 , pp. 714-719
    • Giglia-Mari, G.1    Coin, F.2    Ranish, J.A.3
  • 29
    • 84894494639 scopus 로고    scopus 로고
    • GJC2 promoter mutations causing Pelizaeus-Merzbacher-like disease
    • (3//)
    • Gotoh L., Inoue K., Helman G., et al. GJC2 promoter mutations causing Pelizaeus-Merzbacher-like disease. Mol. Genet. Metab. 2014, 111(3):393-398. (3//).
    • (2014) Mol. Genet. Metab. , vol.111 , Issue.3 , pp. 393-398
    • Gotoh, L.1    Inoue, K.2    Helman, G.3
  • 30
    • 0032823227 scopus 로고    scopus 로고
    • Pulsed magnetization transfer imaging: evaluation of technique
    • (1999/09/01)
    • Graham S.J., Henkelman R.M. Pulsed magnetization transfer imaging: evaluation of technique. Radiology 1999, 212(3):903-910. (1999/09/01).
    • (1999) Radiology , vol.212 , Issue.3 , pp. 903-910
    • Graham, S.J.1    Henkelman, R.M.2
  • 31
    • 84867472678 scopus 로고    scopus 로고
    • Neural stem cell engraftment and myelination in the human brain
    • (October 10, 2012)
    • Gupta N., Henry R.G., Strober J., et al. Neural stem cell engraftment and myelination in the human brain. Sci. Transl. Med. 2012, 4(155):155ra137. (October 10, 2012).
    • (2012) Sci. Transl. Med. , vol.4 , Issue.155 , pp. 155ra137
    • Gupta, N.1    Henry, R.G.2    Strober, J.3
  • 33
    • 80052769310 scopus 로고    scopus 로고
    • Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophy
    • Gv B., Chouery E., Putorti M.L., et al. Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophy. Am. J. Hum. Genet. 2011, 89(3):415-423.
    • (2011) Am. J. Hum. Genet. , vol.89 , Issue.3 , pp. 415-423
    • Gv, B.1    Chouery, E.2    Putorti, M.L.3
  • 34
    • 84903532539 scopus 로고    scopus 로고
    • Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation
    • Hamilton E.M., Polder E., Vanderver A., et al. Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation. Brain 2014, 137(7):1921-1930.
    • (2014) Brain , vol.137 , Issue.7 , pp. 1921-1930
    • Hamilton, E.M.1    Polder, E.2    Vanderver, A.3
  • 35
    • 24644498062 scopus 로고    scopus 로고
    • Quantitative proton MRS of Pelizaeus-Merzbacher disease. Evidence of dys- and hypomyelination
    • Hanefeld F.A., Brockmann K., Pouwels P.J.W., Wilken B., Frahm J., Dechent P. Quantitative proton MRS of Pelizaeus-Merzbacher disease. Evidence of dys- and hypomyelination. Neurology 2005, 65:701-706.
    • (2005) Neurology , vol.65 , pp. 701-706
    • Hanefeld, F.A.1    Brockmann, K.2    Pouwels, P.J.W.3    Wilken, B.4    Frahm, J.5    Dechent, P.6
  • 37
    • 31844433052 scopus 로고    scopus 로고
    • Brain dysmyelination and recovery assessment by noninvasive in vivo diffusion tensor magnetic resonance imaging
    • Harsan L.A., Poulet P., Guignard B., et al. Brain dysmyelination and recovery assessment by noninvasive in vivo diffusion tensor magnetic resonance imaging. J. Neurosci. Res. 2006, 83(3):392-402.
    • (2006) J. Neurosci. Res. , vol.83 , Issue.3 , pp. 392-402
    • Harsan, L.A.1    Poulet, P.2    Guignard, B.3
  • 38
    • 77956985370 scopus 로고    scopus 로고
    • Trichothiodystrophy view from the molecular basis of DNA repair/transcription factor TFIIH
    • (October 15, 2009)
    • Hashimoto S., Egly J.M. Trichothiodystrophy view from the molecular basis of DNA repair/transcription factor TFIIH. Hum. Mol. Genet. 2009, 18(R2):R224-R230. (October 15, 2009).
    • (2009) Hum. Mol. Genet. , vol.18 , Issue.R2 , pp. R224-R230
    • Hashimoto, S.1    Egly, J.M.2
  • 39
  • 40
    • 0027967644 scopus 로고
    • Human nucleotide excision repair syndromes: molecular clues to unexpected intricacies
    • Hoeijmakers J.H.J. Human nucleotide excision repair syndromes: molecular clues to unexpected intricacies. Cancer 1994, 30A:1912-1924.
    • (1994) Cancer , vol.30A , pp. 1912-1924
    • Hoeijmakers, J.H.J.1
  • 42
    • 0343094621 scopus 로고    scopus 로고
    • Microstructural development of human newborn cerebral white matter assessed in vivo by diffusion tensor magnetic resonance imaging
    • Hüppi P., Maier S., Peled S., et al. Microstructural development of human newborn cerebral white matter assessed in vivo by diffusion tensor magnetic resonance imaging. Pediatr. Res. 1998, 44:584-590.
    • (1998) Pediatr. Res. , vol.44 , pp. 584-590
    • Hüppi, P.1    Maier, S.2    Peled, S.3
  • 43
    • 77955660153 scopus 로고    scopus 로고
    • MRI quantification of non-Gaussian water diffusion by kurtosis analysis
    • Jensen J.H., Helpern J.A. MRI quantification of non-Gaussian water diffusion by kurtosis analysis. NMR Biomed. 2010, 23(7):698-710.
    • (2010) NMR Biomed. , vol.23 , Issue.7 , pp. 698-710
    • Jensen, J.H.1    Helpern, J.A.2
  • 44
    • 85028208167 scopus 로고    scopus 로고
    • Neurochemistry in shiverer mouse depicted on MR spectroscopy
    • (n/a-n/a)
    • J-i T., Nitta N., Iwasaki N., et al. Neurochemistry in shiverer mouse depicted on MR spectroscopy. J. Magn. Reson. Imaging 2013, (n/a-n/a).
    • (2013) J. Magn. Reson. Imaging
    • J-i, T.1    Nitta, N.2    Iwasaki, N.3
  • 45
    • 84875234773 scopus 로고    scopus 로고
    • White matter integrity, fiber count, and other fallacies: the do's and don'ts of diffusion MRI
    • (6//)
    • Jones D.K., Knösche T.R., Turner R. White matter integrity, fiber count, and other fallacies: the do's and don'ts of diffusion MRI. NeuroImage 2013, 73(0):239-254. (6//).
    • (2013) NeuroImage , vol.73 , pp. 239-254
    • Jones, D.K.1    Knösche, T.R.2    Turner, R.3
  • 46
    • 84991209261 scopus 로고    scopus 로고
    • Altered PLP1 splicing causes hypomyelination of early myelinating structures
    • Kevelam S.H., Taube J.R., van Spaendonk R.M.L., et al. Altered PLP1 splicing causes hypomyelination of early myelinating structures. Ann. Clin. Transl. Neurol. 2015, 2(6):648-661.
    • (2015) Ann. Clin. Transl. Neurol. , vol.2 , Issue.6 , pp. 648-661
    • Kevelam, S.H.1    Taube, J.R.2    van Spaendonk, R.M.L.3
  • 47
    • 0023885478 scopus 로고
    • Sequence of central nervous system myelination in human infancy. II. Patterns of myelination in autopsied infants
    • Kinney H.C., Brody B.A., Kloman A.S., Gilles F.H. Sequence of central nervous system myelination in human infancy. II. Patterns of myelination in autopsied infants. J. Neuropathol. Exp. Neurol. 1988, 47:217-234.
    • (1988) J. Neuropathol. Exp. Neurol. , vol.47 , pp. 217-234
    • Kinney, H.C.1    Brody, B.A.2    Kloman, A.S.3    Gilles, F.H.4
  • 48
    • 0023153460 scopus 로고
    • Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease
    • Koeppen A.H., Ronca N.A., Greenfield E., Hans M.B. Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease. Ann. Neurol. 1987, 21:159-170.
    • (1987) Ann. Neurol. , vol.21 , pp. 159-170
    • Koeppen, A.H.1    Ronca, N.A.2    Greenfield, E.3    Hans, M.B.4
  • 49
    • 84892714156 scopus 로고    scopus 로고
    • Brain magnetic resonance imaging (MRI) pattern recognition in Pol III-related leukodystrophies
    • February 1, 2014
    • La Piana R., Tonduti D., Dressman H.G., et al. Brain magnetic resonance imaging (MRI) pattern recognition in Pol III-related leukodystrophies. J. Child Neurol. 2014, 29(2):214-220. February 1, 2014.
    • (2014) J. Child Neurol. , vol.29 , Issue.2 , pp. 214-220
    • La Piana, R.1    Tonduti, D.2    Dressman, H.G.3
  • 50
    • 84890797506 scopus 로고    scopus 로고
    • Myelin water mapping by spatially regularized longitudinal relaxographic imaging at high magnetic fields
    • Labadie C., Lee J.-H., Rooney W.D., et al. Myelin water mapping by spatially regularized longitudinal relaxographic imaging at high magnetic fields. Magn. Reson. Med. 2014, 71(1):375-387.
    • (2014) Magn. Reson. Med. , vol.71 , Issue.1 , pp. 375-387
    • Labadie, C.1    Lee, J.-H.2    Rooney, W.D.3
  • 51
    • 84872872374 scopus 로고    scopus 로고
    • On the inherent precision of mcDESPOT
    • 03/12
    • Lankford C.L., Does M.D. On the inherent precision of mcDESPOT. Magn. Reson. Med. 2013, 69(1):127-136. 03/12.
    • (2013) Magn. Reson. Med. , vol.69 , Issue.1 , pp. 127-136
    • Lankford, C.L.1    Does, M.D.2
  • 52
    • 73149102998 scopus 로고    scopus 로고
    • Characterizing healthy and diseased white matter using quantitative magnetization transfer and multicomponent T2 relaxometry: a unified view via a four-pool model
    • Levesque I.R., Pike G.B. Characterizing healthy and diseased white matter using quantitative magnetization transfer and multicomponent T2 relaxometry: a unified view via a four-pool model. Magn. Reson. Med. 2009, 62(6):1487-1496.
    • (2009) Magn. Reson. Med. , vol.62 , Issue.6 , pp. 1487-1496
    • Levesque, I.R.1    Pike, G.B.2
  • 53
    • 0025222748 scopus 로고
    • Developmental expression of proteolipid protein and DM20 mRNAs and proteins in the rat brain
    • LeVine S.M., Wong D., Macklin W.B. Developmental expression of proteolipid protein and DM20 mRNAs and proteins in the rat brain. Dev. Neurosci. 1990, 12(4-5):235-250.
    • (1990) Dev. Neurosci. , vol.12 , Issue.4-5 , pp. 235-250
    • LeVine, S.M.1    Wong, D.2    Macklin, W.B.3
  • 54
    • 32444432752 scopus 로고    scopus 로고
    • 18q deletions: clinical, molecular, and brain MRI findings of 14 individuals
    • Linnankivi T., Tienari P., Somer M., et al. 18q deletions: clinical, molecular, and brain MRI findings of 14 individuals. Am. J. Med. Genet. A 2006, 140A(4):331-339.
    • (2006) Am. J. Med. Genet. A , vol.140A , Issue.4 , pp. 331-339
    • Linnankivi, T.1    Tienari, P.2    Somer, M.3
  • 55
    • 0028338642 scopus 로고
    • In vivo visualization of myelin water in brain by magnetic resonance
    • Mackay A., Whittall K., Adler J., Li D., Paty D., Graeb D. In vivo visualization of myelin water in brain by magnetic resonance. Magn. Reson. Med. 1994, 31(6):673-677.
    • (1994) Magn. Reson. Med. , vol.31 , Issue.6 , pp. 673-677
    • Mackay, A.1    Whittall, K.2    Adler, J.3    Li, D.4    Paty, D.5    Graeb, D.6
  • 58
    • 0025856859 scopus 로고
    • Multiexponential proton relaxation in model cellular systems
    • Menon R.S., Rusinko M.S., Allen P.S. Multiexponential proton relaxation in model cellular systems. Magn. Reson. Med. 1991, 20(2):196-213.
    • (1991) Magn. Reson. Med. , vol.20 , Issue.2 , pp. 196-213
    • Menon, R.S.1    Rusinko, M.S.2    Allen, P.S.3
  • 59
    • 82255175854 scopus 로고    scopus 로고
    • Promoter mutation is a common variant in GJC2-associated Pelizaeus-Merzbacher-like disease
    • Meyer E., Kurian M.A., Morgan N.V., et al. Promoter mutation is a common variant in GJC2-associated Pelizaeus-Merzbacher-like disease. Mol. Genet. Metab. 2011, 104(4):637-643.
    • (2011) Mol. Genet. Metab. , vol.104 , Issue.4 , pp. 637-643
    • Meyer, E.1    Kurian, M.A.2    Morgan, N.V.3
  • 60
    • 0029071158 scopus 로고
    • Oculodentodigital dysplasia with cerebral white matter abnormalities in a two-generation family
    • Norton K., Carey J.C., Gutmann D.H. Oculodentodigital dysplasia with cerebral white matter abnormalities in a two-generation family. Am. J. Med. Genet. 1995, 57:458-461.
    • (1995) Am. J. Med. Genet. , vol.57 , pp. 458-461
    • Norton, K.1    Carey, J.C.2    Gutmann, D.H.3
  • 61
    • 84862495187 scopus 로고    scopus 로고
    • Deep gray matter maturation in very preterm neonates: regional variations and pathology-related age-dependent changes in magnetization transfer ratio
    • (2012/05/01)
    • Nossin-Manor R., Chung A.D., Whyte H.E.A., Shroff M.M., Taylor M.J., Sled J.G. Deep gray matter maturation in very preterm neonates: regional variations and pathology-related age-dependent changes in magnetization transfer ratio. Radiology 2012, 263(2):510-517. (2012/05/01).
    • (2012) Radiology , vol.263 , Issue.2 , pp. 510-517
    • Nossin-Manor, R.1    Chung, A.D.2    Whyte, H.E.A.3    Shroff, M.M.4    Taylor, M.J.5    Sled, J.G.6
  • 62
    • 84867449241 scopus 로고    scopus 로고
    • Quantitative MRI in the very preterm brain: assessing tissue organization and myelination using magnetization transfer, diffusion tensor and T1 imaging
    • (1/1/)
    • Nossin-Manor R., Card D., Morris D., et al. Quantitative MRI in the very preterm brain: assessing tissue organization and myelination using magnetization transfer, diffusion tensor and T1 imaging. NeuroImage 2013, 64(0):505-516. (1/1/).
    • (2013) NeuroImage , vol.64 , pp. 505-516
    • Nossin-Manor, R.1    Card, D.2    Morris, D.3
  • 63
    • 84875192186 scopus 로고    scopus 로고
    • Depletion of molecular chaperones from the endoplasmic reticulum and fragmentation of the Golgi apparatus associated with pathogenesis in Pelizaeus-Merzbacher disease
    • March 15, 2013
    • Numata Y., Morimura T., Nakamura S., et al. Depletion of molecular chaperones from the endoplasmic reticulum and fragmentation of the Golgi apparatus associated with pathogenesis in Pelizaeus-Merzbacher disease. J. Biol. Chem. 2013, 288(11)):7451-7466. March 15, 2013.
    • (2013) J. Biol. Chem. , vol.288 , Issue.11 , pp. 7451-7466
    • Numata, Y.1    Morimura, T.2    Nakamura, S.3
  • 64
    • 23844436002 scopus 로고    scopus 로고
    • MR properties of excised neural tissue following experimentally induced demyelination
    • Odrobina E.E., Lam T.Y.J., Pun T., Midha R., Stanisz G.J. MR properties of excised neural tissue following experimentally induced demyelination. NMR Biomed. 2005, 18(5):277-284.
    • (2005) NMR Biomed. , vol.18 , Issue.5 , pp. 277-284
    • Odrobina, E.E.1    Lam, T.Y.J.2    Pun, T.3    Midha, R.4    Stanisz, G.J.5
  • 65
    • 0030473218 scopus 로고    scopus 로고
    • The central nervous system in Tay syndrome
    • Ostergaard J.R., Christensen T. The central nervous system in Tay syndrome. Neuropediatrics 1996, 27:326-330.
    • (1996) Neuropediatrics , vol.27 , pp. 326-330
    • Ostergaard, J.R.1    Christensen, T.2
  • 66
    • 0030473218 scopus 로고    scopus 로고
    • The central nervous system in Tay syndrome
    • Østergaard J.R., Christensen T. The central nervous system in Tay syndrome. Neuropediatrics 1996, 27:326-330.
    • (1996) Neuropediatrics , vol.27 , pp. 326-330
    • Østergaard, J.R.1    Christensen, T.2
  • 67
    • 0035065006 scopus 로고    scopus 로고
    • Maturation of white matter in the human brain: a review of magnetic resonance studies
    • (2//)
    • Paus T., Collins D.L., Evans A.C., Leonard G., Pike B., Zijdenbos A. Maturation of white matter in the human brain: a review of magnetic resonance studies. Brain Res. Bull. 2001, 54(3):255-266. (2//).
    • (2001) Brain Res. Bull. , vol.54 , Issue.3 , pp. 255-266
    • Paus, T.1    Collins, D.L.2    Evans, A.C.3    Leonard, G.4    Pike, B.5    Zijdenbos, A.6
  • 68
    • 66749106316 scopus 로고    scopus 로고
    • GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype
    • Paznekas W.A., Karczeski B., Vermeer S., et al. GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype. Hum. Mutat. 2009, 30(5):724-733.
    • (2009) Hum. Mutat. , vol.30 , Issue.5 , pp. 724-733
    • Paznekas, W.A.1    Karczeski, B.2    Vermeer, S.3
  • 69
    • 0029908076 scopus 로고    scopus 로고
    • Toward a quantitative assessment of diffusion anisotropy
    • Pierpaoli C., Basser P.J. Toward a quantitative assessment of diffusion anisotropy. Magn. Reson. Med. 1996, 36(6):893-906.
    • (1996) Magn. Reson. Med. , vol.36 , Issue.6 , pp. 893-906
    • Pierpaoli, C.1    Basser, P.J.2
  • 70
    • 84922260233 scopus 로고    scopus 로고
    • TUBB4A de novo mutations cause isolated hypomyelination
    • (02/07/received 06/02/accepted)
    • Pizzino A., Pierson T.M., Guo Y., et al. TUBB4A de novo mutations cause isolated hypomyelination. Neurology 2014, 83(10):898-902. (02/07/received 06/02/accepted).
    • (2014) Neurology , vol.83 , Issue.10 , pp. 898-902
    • Pizzino, A.1    Pierson, T.M.2    Guo, Y.3
  • 72
    • 84904750732 scopus 로고    scopus 로고
    • Hypomyelinating leukodystrophies: translational research progress and prospects
    • Pouwels P.J.W., Vanderver A., Bernard G., et al. Hypomyelinating leukodystrophies: translational research progress and prospects. Ann. Neurol. 2014, 76(1):5-19.
    • (2014) Ann. Neurol. , vol.76 , Issue.1 , pp. 5-19
    • Pouwels, P.J.W.1    Vanderver, A.2    Bernard, G.3
  • 73
    • 0034831377 scopus 로고    scopus 로고
    • Visualization of nonstructural changes in early white matter development on diffusion weighted MR images: evidence supporting premyelination anisotropy
    • Prayer D., Barkovich A.J., Kirschner D.A., et al. Visualization of nonstructural changes in early white matter development on diffusion weighted MR images: evidence supporting premyelination anisotropy. AJNR Am. J. Neuroradiol. 2001, 22:1572-1576.
    • (2001) AJNR Am. J. Neuroradiol. , vol.22 , pp. 1572-1576
    • Prayer, D.1    Barkovich, A.J.2    Kirschner, D.A.3
  • 74
    • 84855306010 scopus 로고    scopus 로고
    • High-resolution diffusion tensor imaging of fixed brain in a mouse model of Pelizaeus-Merzbacher disease: comparison with quantitative measures of white matter pathology
    • Ruest T., Holmes W.M., Barrie J.A., et al. High-resolution diffusion tensor imaging of fixed brain in a mouse model of Pelizaeus-Merzbacher disease: comparison with quantitative measures of white matter pathology. NMR Biomed. 2011, 24:1369-1379.
    • (2011) NMR Biomed. , vol.24 , pp. 1369-1379
    • Ruest, T.1    Holmes, W.M.2    Barrie, J.A.3
  • 76
    • 62349126641 scopus 로고    scopus 로고
    • Invited article: an MRI-based approach to the diagnosis of white matter disorders
    • Schiffmann R., van der Knaap M.S. Invited article: an MRI-based approach to the diagnosis of white matter disorders. Neurology 2009, 72(8):750-759.
    • (2009) Neurology , vol.72 , Issue.8 , pp. 750-759
    • Schiffmann, R.1    van der Knaap, M.S.2
  • 77
    • 0028351908 scopus 로고
    • Childhood ataxia with diffuse central nervous system hypomyelination
    • Schiffmann R., Moller J.R., Trapp B.D., et al. Childhood ataxia with diffuse central nervous system hypomyelination. Ann. Neurol. 1994, 35:331-340.
    • (1994) Ann. Neurol. , vol.35 , pp. 331-340
    • Schiffmann, R.1    Moller, J.R.2    Trapp, B.D.3
  • 78
    • 34547809867 scopus 로고    scopus 로고
    • Quantitative magnetization transfer imaging in postmortem multiple sclerosis brain
    • Schmierer K., Tozer D.J., Scaravilli F., et al. Quantitative magnetization transfer imaging in postmortem multiple sclerosis brain. J. Magn. Reson. Imaging 2007, 26(1):41-51.
    • (2007) J. Magn. Reson. Imaging , vol.26 , Issue.1 , pp. 41-51
    • Schmierer, K.1    Tozer, D.J.2    Scaravilli, F.3
  • 79
    • 84877586063 scopus 로고    scopus 로고
    • A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum
    • (0)
    • Simons C., Wolf Nicole I., McNeil N., et al. A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum. Am. J. Hum. Genet. 2013, (0).
    • (2013) Am. J. Hum. Genet.
    • Simons, C.1    Wolf Nicole, I.2    McNeil, N.3
  • 80
    • 0031801082 scopus 로고    scopus 로고
    • Duplication of the proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease
    • Sistermans E.A., de Coo rFM., De Wijs I.J., Van Oost B.A. 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, R.2    De Wijs, I.J.3    Van Oost, B.A.4
  • 81
    • 0034759242 scopus 로고    scopus 로고
    • Quantitative imaging of magnetization transfer exchange and relaxation properties in vivo using MRI
    • Sled J.G., Pike G.B. Quantitative imaging of magnetization transfer exchange and relaxation properties in vivo using MRI. Magn. Reson. Med. 2001, 46(5):923-931.
    • (2001) Magn. Reson. Med. , vol.46 , Issue.5 , pp. 923-931
    • Sled, J.G.1    Pike, G.B.2
  • 82
    • 0036430645 scopus 로고    scopus 로고
    • Dysmyelination revealed through MRI as increased radial (but unchanged axial) diffusion of water
    • Song S.-K., Sun S.-W., Ramsbottom M.J., Chang C., Russell J., Cross A.H. Dysmyelination revealed through MRI as increased radial (but unchanged axial) diffusion of water. NeuroImage 2002, 17(3):1429.
    • (2002) NeuroImage , vol.17 , Issue.3 , pp. 1429
    • Song, S.-K.1    Sun, S.-W.2    Ramsbottom, M.J.3    Chang, C.4    Russell, J.5    Cross, A.H.6
  • 83
    • 0037079142 scopus 로고    scopus 로고
    • The unfolded protein response modulates disease severity in Pelizaeus-Merzbacher disease
    • Southwood C.M., Garbern J.Y., Jiang W., Gow A. The unfolded protein response modulates disease severity in Pelizaeus-Merzbacher disease. Neuron 2002, 36(4):585-596.
    • (2002) Neuron , vol.36 , Issue.4 , pp. 585-596
    • Southwood, C.M.1    Garbern, J.Y.2    Jiang, W.3    Gow, A.4
  • 85
    • 77957688535 scopus 로고    scopus 로고
    • Magnetic resonance imaging pattern recognition in hypomyelinating disorders
    • Steenweg M., Vanderver A., Blaser S., et al. Magnetic resonance imaging pattern recognition in hypomyelinating disorders. Brain 2010, 133:2971-2982.
    • (2010) Brain , vol.133 , pp. 2971-2982
    • Steenweg, M.1    Vanderver, A.2    Blaser, S.3
  • 86
    • 84890878934 scopus 로고    scopus 로고
    • MR spectroscopy in 18q-syndrome suggesting other than hypomyelination
    • (1//)
    • Tada H., Takanashi J.-i. MR spectroscopy in 18q-syndrome suggesting other than hypomyelination. Brain Dev. 2014, 36(1):57-60. (1//).
    • (2014) Brain Dev. , vol.36 , Issue.1 , pp. 57-60
    • Tada, H.1    Takanashi, J.-I.2
  • 87
    • 84877252262 scopus 로고    scopus 로고
    • Mutations in DARS cause hypomyelination with brain stem and spinal cord involvement and leg spasticity
    • Taft R., Vanderver A., Leventer Richard J., et al. Mutations in DARS cause hypomyelination with brain stem and spinal cord involvement and leg spasticity. Am. J. Hum. Genet. 2013, 92(5):774-780.
    • (2013) Am. J. Hum. Genet. , vol.92 , Issue.5 , pp. 774-780
    • Taft, R.1    Vanderver, A.2    Leventer Richard, J.3
  • 88
    • 0037154241 scopus 로고    scopus 로고
    • Brain N-acetylaspartate is elevated in Pelizaeus-Merzbacher disease with PLP1 duplication
    • Takanashi J., Inoue K., Tomita M., et al. Brain N-acetylaspartate is elevated in Pelizaeus-Merzbacher disease with PLP1 duplication. Neurology 2002, 58:237-241.
    • (2002) Neurology , vol.58 , pp. 237-241
    • Takanashi, J.1    Inoue, K.2    Tomita, M.3
  • 90
    • 84856968869 scopus 로고    scopus 로고
    • Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination
    • Tanaka R., Iwasaki N., Hayashi M., et al. Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination. Brain Dev. 2012, 34(3):234-237.
    • (2012) Brain Dev. , vol.34 , Issue.3 , pp. 234-237
    • Tanaka, R.1    Iwasaki, N.2    Hayashi, M.3
  • 91
    • 84884593171 scopus 로고    scopus 로고
    • Novel FAM126A mutations in hypomyelination and congenital cataract disease
    • (9/27/)
    • Traverso M., Assereto S., Gazzerro E., et al. Novel FAM126A mutations in hypomyelination and congenital cataract disease. Biochem. Biophys. Res. Commun. 2013, 439(3):369-372. (9/27/).
    • (2013) Biochem. Biophys. Res. Commun. , vol.439 , Issue.3 , pp. 369-372
    • Traverso, M.1    Assereto, S.2    Gazzerro, E.3
  • 92
    • 84867452128 scopus 로고    scopus 로고
    • Human neural stem cells induce functional myelination in mice with severe dysmyelination
    • 155ra136 (October 10, 2012)
    • Uchida N., Chen K., Dohse M., et al. Human neural stem cells induce functional myelination in mice with severe dysmyelination. Sci. Transl. Med. 2012, 4(155):155ra136. (October 10, 2012).
    • (2012) Sci. Transl. Med. , vol.4 , Issue.155
    • Uchida, N.1    Chen, K.2    Dohse, M.3
  • 93
    • 38349192870 scopus 로고    scopus 로고
    • A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract
    • Ugur S.A., Tolun A. A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract. Eur. J. Hum. Genet. 2008, 16:261-264.
    • (2008) Eur. J. Hum. Genet. , vol.16 , pp. 261-264
    • Ugur, S.A.1    Tolun, A.2
  • 94
    • 3242693178 scopus 로고    scopus 로고
    • Mutations in the gene encoding gap junction protein alpha-12 (Connexin 46.6) cause Pelizaeus-Merzbacher-like disease
    • Uhlenberg B., Schuelke M., Rüschendorf F., et al. Mutations in the gene encoding gap junction protein alpha-12 (Connexin 46.6) cause Pelizaeus-Merzbacher-like disease. Am. J. Hum. Genet. 2004, 75(2):251-260.
    • (2004) Am. J. Hum. Genet. , vol.75 , Issue.2 , pp. 251-260
    • Uhlenberg, B.1    Schuelke, M.2    Rüschendorf, F.3
  • 95
    • 0003567951 scopus 로고    scopus 로고
    • Pelizaeus Merzbacher disease and X-linked spastic paraplegia type 2
    • Springer, Berlin, M.S. van der Knaap, J. Valk (Eds.)
    • van der Knaap M.S., Valk J. Pelizaeus Merzbacher disease and X-linked spastic paraplegia type 2. Magnetic Resonance of Myelin, Myelination, and Myelin Disorders 2005, 272-280. Springer, Berlin. 3rd ed. M.S. van der Knaap, J. Valk (Eds.).
    • (2005) Magnetic Resonance of Myelin, Myelination, and Myelin Disorders , pp. 272-280
    • van der Knaap, M.S.1    Valk, J.2
  • 98
    • 34447317261 scopus 로고    scopus 로고
    • Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology
    • van der Knaap M., Linnankivi T., Paetau A., et al. Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology. Neurology 2007, 69:166-171.
    • (2007) Neurology , vol.69 , pp. 166-171
    • van der Knaap, M.1    Linnankivi, T.2    Paetau, A.3
  • 99
    • 84872716294 scopus 로고    scopus 로고
    • Multimodality evaluation of the pediatric brain: DTI and its competitors
    • (2013/01/01)
    • Vasung L., Fischi-Gomez E., Hüppi P. Multimodality evaluation of the pediatric brain: DTI and its competitors. Pediatr. Radiol. 2013, 43(1):60-68. (2013/01/01).
    • (2013) Pediatr. Radiol. , vol.43 , Issue.1 , pp. 60-68
    • Vasung, L.1    Fischi-Gomez, E.2    Hüppi, P.3
  • 100
    • 84885727788 scopus 로고    scopus 로고
    • Microtubule-depolymerizing kinesins
    • (2013/10/06)
    • Walczak C.E., Gayek S., Ohi R. Microtubule-depolymerizing kinesins. Annu. Rev. Cell Dev. Biol. 2013, 29(1):417-441. (2013/10/06).
    • (2013) Annu. Rev. Cell Dev. Biol. , vol.29 , Issue.1 , pp. 417-441
    • Walczak, C.E.1    Gayek, S.2    Ohi, R.3
  • 101
    • 16944363270 scopus 로고    scopus 로고
    • A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy
    • Weeda G., Eveno E., Donker I., et al. A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy. Am. J. Hum. Genet. 1997, 60:320-329.
    • (1997) Am. J. Hum. Genet. , vol.60 , pp. 320-329
    • Weeda, G.1    Eveno, E.2    Donker, I.3
  • 103
    • 84862178407 scopus 로고    scopus 로고
    • Direct magnetic resonance detection of myelin and prospects for quantitative imaging of myelin density
    • (June 12, 2012)
    • Wilhelm M.J., Ong H.H., Wehrli S.L., et al. Direct magnetic resonance detection of myelin and prospects for quantitative imaging of myelin density. Proc. Natl. Acad. Sci. 2012, 109(24):9605-9610. (June 12, 2012).
    • (2012) Proc. Natl. Acad. Sci. , vol.109 , Issue.24 , pp. 9605-9610
    • Wilhelm, M.J.1    Ong, H.H.2    Wehrli, S.L.3
  • 105
    • 20244380309 scopus 로고    scopus 로고
    • Leukoencephalopathy with ataxia, hypodontia, and hypomyelination
    • Wolf N.I., Harting I., Boltshauser E., et al. Leukoencephalopathy with ataxia, hypodontia, and hypomyelination. Neurology 2005, 64(8):1461-1464.
    • (2005) Neurology , vol.64 , Issue.8 , pp. 1461-1464
    • Wolf, N.I.1    Harting, I.2    Boltshauser, E.3
  • 106
    • 34548741364 scopus 로고    scopus 로고
    • Ataxia, delayed dentition and hypomyelination: a novel leukoencephalopathy
    • Wolf N.I., Harting I., Innes A.M., et al. Ataxia, delayed dentition and hypomyelination: a novel leukoencephalopathy. Neuropediatrics 2007, 38(2):64-70.
    • (2007) Neuropediatrics , vol.38 , Issue.2 , pp. 64-70
    • Wolf, N.I.1    Harting, I.2    Innes, A.M.3
  • 107
    • 84904820980 scopus 로고    scopus 로고
    • Mutations in RARS cause hypomyelination
    • Wolf N.I., Salomons G.S., Rodenburg R.J., et al. Mutations in RARS cause hypomyelination. Ann. Neurol. 2014, 76(1):134-139.
    • (2014) Ann. Neurol. , vol.76 , Issue.1 , pp. 134-139
    • Wolf, N.I.1    Salomons, G.S.2    Rodenburg, R.J.3
  • 108
    • 33644668804 scopus 로고    scopus 로고
    • A three-dimensional working model of the multienzyme complex of aminoacyl-tRNA synthetases based on electron microscopic placements of tRNA and proteins
    • (November 18, 2005)
    • Wolfe C.L., Warrington J.A., Treadwell L., Norcum M.T. A three-dimensional working model of the multienzyme complex of aminoacyl-tRNA synthetases based on electron microscopic placements of tRNA and proteins. J. Biol. Chem. 2005, 280(46):38870-38878. (November 18, 2005).
    • (2005) J. Biol. Chem. , vol.280 , Issue.46 , pp. 38870-38878
    • Wolfe, C.L.1    Warrington, J.A.2    Treadwell, L.3    Norcum, M.T.4
  • 109
    • 0024573913 scopus 로고
    • Magnetization transfer contrast (MTC) and tissue water proton relaxation in vivo
    • Wolff S.D., Balaban R.S. Magnetization transfer contrast (MTC) and tissue water proton relaxation in vivo. Magn. Reson. Med. 1989, 11:135-144.
    • (1989) Magn. Reson. Med. , vol.11 , pp. 135-144
    • Wolff, S.D.1    Balaban, R.S.2
  • 110
    • 0001862032 scopus 로고
    • The myelogenetic cycles of regional maturation of the brain
    • Blackwell, Oxford, A. Minkowski (Ed.)
    • Yakovlev P.I., Lecours A.R. The myelogenetic cycles of regional maturation of the brain. Regional Development of the Brain in Early Life 1967, 3-70. Blackwell, Oxford. A. Minkowski (Ed.).
    • (1967) Regional Development of the Brain in Early Life , pp. 3-70
    • Yakovlev, P.I.1    Lecours, A.R.2
  • 111
    • 33749143617 scopus 로고    scopus 로고
    • Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract
    • Zara F., Biancheri R., Bruno C., et al. Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract. Nat. Genet. 2006, 38(10):1111-1113.
    • (2006) Nat. Genet. , vol.38 , Issue.10 , pp. 1111-1113
    • Zara, F.1    Biancheri, R.2    Bruno, C.3


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