Research ArticlePEDIATRICS
Open Access
Temporal and Spatial Development of Axonal Maturation and Myelination of White Matter in the Developing Brain
W. Gao, W. Lin, Y. Chen, G. Gerig, J.K. Smith, V. Jewells and J.H. Gilmore
American Journal of Neuroradiology February 2009, 30 (2) 290-296; DOI: https://doi.org/10.3174/ajnr.A1363
W. Gao
W. Lin
Y. Chen
G. Gerig
J.K. Smith
V. Jewells

References
- ↵McGraw P, Liang L, Provenzale JM. Evaluation of normal age-related changes in anisotropy during infancy and childhood as shown by diffusion tensor imaging. AJR Am J Roentgenol 2002;179:1515–22
- ↵Mukherjee P, Miller JH, Shimony JS, et al. Diffusion-tensor MR imaging of gray and white matter development during normal human brain maturation. AJNR Am J Neuroradiol 2002;23:1445–56
- ↵Partridge SC, Mukherjee P, Henry RG, et al. Diffusion tensor imaging: serial quantitation of white matter tract maturity in premature newborns. Neuroimage 2004;22:1302–14
- ↵Haynes RL, Borenstein NS, Desilva TM, et al. Axonal development in the cerebral white matter of the human fetus and infant. J Comp Neurol 2005;484:156–67
- ↵Schneider JF, Il'yasov KA, Hennig J, et al. Fast quantitative diffusion-tensor imaging of cerebral white matter from the neonatal period to adolescence. Neuroradiology 2004;46:258–66. Epub 2004 Mar 4
- ↵Huppi PS, Maier SE, Peled S, et al. Microstructural development of human newborn cerebral white matter assessed in vivo by diffusion tensor magnetic resonance imaging. Pediatr Res 1998;44:584–90
- ↵Counsell SJ, Shen Y, Boardman JP, et al. Axial and radial diffusivity in preterm infants who have diffuse white matter changes on magnetic resonance imaging at term-equivalent age. Pediatrics 2006;117:376–86
- ↵Schmithorst VJ, Wilke M, Dardzinski BJ, et al. Correlation of white matter diffusivity and anisotropy with age during childhood and adolescence: a cross-sectional diffusion-tensor MR imaging study. Radiology 2002;222:212–18
- ↵Snook L, Paulson LA, Roy D, et al. Diffusion tensor imaging of neurodevelopment in children and young adults. Neuroimage 2005;26:1164–73
- ↵Mukherjee P, Miller JH, Shimony JS, et al. Normal brain maturation during childhood: developmental trends characterized with diffusion-tensor MR imaging. Radiology 2001;221:349–58
- Miller JH, McKinstry RC, Philip JV, et al. Diffusion-tensor MR imaging of normal brain maturation: a guide to structural development and myelination. AJR Am J Roentgenol 2003;180:851–59
- ↵Hermoye L, Saint-Martin C, Cosnard G, et al. Pediatric diffusion tensor imaging: normal database and observation of the white matter maturation in early childhood. Neuroimage 2006;29:493–504
- ↵Zhai G, Lin W, Wilber KP, et al. Comparisons of regional white matter diffusion in healthy neonates and adults performed with a 3.0-T head-only MR imaging unit. Radiology 2003;229:673–81
- ↵Basser PJ. Inferring microstructural features and the physiological state of tissues from diffusion-weighted images. NMR Biomed 1995;8:333–44
- Basser PJ, Pajevic S, Pierpaoli C, et al. In vivo fiber tractography using DT-MRI data. Magn Reson Med 2000;44:625–32
- ↵Xue R, van Zijl PC, Crain BJ, et al. In vivo three-dimensional reconstruction of rat brain axonal projections by diffusion tensor imaging. Magn Reson Med 1999;42:1123–27
- ↵Song SK, Sun SW, Ju WK, et al. Diffusion tensor imaging detects and differentiates axon and myelin degeneration in mouse optic nerve after retinal ischemia. Neuroimage 2003;20:1714–22
- ↵Song SK, Yoshino J, Le TQ, et al. Demyelination increases radial diffusivity in corpus callosum of mouse brain. Neuroimage 2005;26:132–40
- ↵Budde MD, Kim JH, Liang HF, et al. Toward accurate diagnosis of white matter pathology using diffusion tensor imaging. Magn Reson Med 2007;57:688–95
- ↵Gilmore JH, Lin W, Prastawa MW, et al. Regional gray matter growth, sexual dimorphism, and cerebral asymmetry in the neonatal brain. J Neurosci 2007;27:1255–60
- ↵Pierpaoli C, Basser PJ. Toward a quantitative assessment of diffusion anisotropy. Magn Reson Med 1996;36:893–906
- Basser PJ, Pierpaoli C. Microstructural and physiological features of tissues elucidated by quantitative-diffusion-tensor MRI. J Magn Reson B 1996;111:209–19
- ↵Basser PJ, Mattiello J, LeBihan D. Estimation of the effective self-diffusion tensor from the NMR spin echo. J Magn Reson B 1994;103:247–54
- ↵Huang H, Zhang J, Wakana S, et al. White and gray matter development in human fetal, newborn and pediatric brains. Neuroimage 2006;33:27–38
- ↵Gilmore JH, Lin W, Corouge I, et al. Early postnatal development of corpus callosum and corticospinal white matter assessed with quantitative tractography. AJNR Am J Neuroradiol 2007;28:1789–95
- ↵Dobbing J, Sands J. Quantitative growth and development of human brain. Arch Dis Child 1973;48:757–67
- ↵Flechsig P. Developmental (myelogenetic) localisation of the cerebral cortex in the human. Lancet 1901;158:1027–30
- Keene MFL, Hewer EE. Some observations on myelination in the human central nervous system. J Anat 1931;66:1–13
- Kinney HC, Brody BA, Kloman AS, et al. Sequence of central nervous system myelination in human infancy. II. Patterns of myelination in autopsied infants. J Neuropathol Exp Neurol 1988;47:217–34
- ↵Yakovlev P, Lecours A. The myelogenetic cycles of regional maturation of the brain. In: Minkowski A, ed. Regional Development of the Brain in Early Life. Oxford, UK: Blackwell;1967 :3–70
- ↵Volpe JJ. Neurology of the Newborn. Philadelphia: Saunders;1995
- ↵Ashtari M, Cervellione KL, Hasan KM, et al. White matter development during late adolescence in healthy males: a cross-sectional diffusion tensor imaging study. Neuroimage 2007;35:501–10
- ↵Kantor DB, Kolodkin AL. Curbing the excesses of youth: molecular insights into axonal pruning. Neuron 2003;38:849–52
- ↵Richards LJ, Plachez C, Ren T. Mechanisms regulating the development of the corpus callosum and its agenesis in mouse and human. Clin Genet 2004;66:276–89
- ↵Bockhorst KH, Narayana PA, Liu R, et al. Early postnatal development of rat brain: in vivo diffusion tensor imaging. J Neurosci Res 2008;86:1520–28
- ↵
- ↵Jones DK. The effect of gradient sampling schemes on measures derived from diffusion tensor MRI: a Monte Carlo study. Magn Reson Med 2004;51:807–15
- ↵Jones DK, Horsfield MA, Simmons A. Optimal strategies for measuring diffusion in anisotropic systems by magnetic resonance imaging. Magn Reson Med 1999;42:515–25
- ↵Kim JH, Loy DN, Liang HF, et al. Noninvasive diffusion tensor imaging of evolving white matter pathology in a mouse model of acute spinal cord injury. Magn Reson Med 2007;58:253–60
- ↵
In this issue
Advertisement
Temporal and Spatial Development of Axonal Maturation and Myelination of White Matter in the Developing Brain
W. Gao, W. Lin, Y. Chen, G. Gerig, J.K. Smith, V. Jewells, J.H. Gilmore
American Journal of Neuroradiology Feb 2009, 30 (2) 290-296; DOI: 10.3174/ajnr.A1363
Jump to section
Related Articles
- No related articles found.
Cited By...
- Two Axes of White Matter Development
- Dynamics of infant white matter maturation from birth to 6 months
- Baby Open Brains: An Open-Source Repository of Infant Brain Segmentations
- Prenatal Exposure to Early Life Adversity and Neonatal Brain Volumes at Birth
- Correlation between Cranial Nerve Microstructural Characteristics and Vestibular Schwannoma Tumor Volume
- Waves of Maturation and Senescence in Micro-Structural MRI Markers of Human Cortical Myelination over the Lifespan
- Common and heritable components of white matter microstructure predict cognitive function at 1 and 2 y
- Longitudinal Study of the Emerging Functional Connectivity Asymmetry of Primary Language Regions during Infancy
- Intersubject Variability of and Genetic Effects on the Brain's Functional Connectivity during Infancy
- Development of Thalamocortical Connectivity during Infancy and Its Cognitive Correlations
- DTI Values in Key White Matter Tracts from Infancy through Adolescence
- Comparison of Spin-Echo T1- and T2-Weighted and Gradient-Echo T1-Weighted Images at 3T in Evaluating Very Preterm Neonates at Term-Equivalent Age
- Abnormal Interhemispheric Connectivity in Neonates with D-Transposition of the Great Arteries Undergoing Cardiopulmonary Bypass Surgery
- The Diffusion Tensor Imaging Toolbox
- Latency Measures of Pattern-Reversal VEP in Adults and Infants: Different Information from Transient P1 Response and Steady-State Phase
This article has not yet been cited by articles in journals that are participating in Crossref Cited-by Linking.
More in this TOC Section
Similar Articles
Advertisement